What is Rhabdomyosarcoma?

Prepare. Communicate. Find Support.

Read our Comprehensive Guide for the Newly Diagnosed

There are two kinds of muscle cells in the body: smooth muscle cells and skeletal muscle cells. Smooth muscles control involuntary activities; skeletal muscles control voluntary activities. Rhabdomyosarcoma (RMS) is a malignant tumor ("cancer") that arises from a normal skeletal muscle cell. Not very much is known about why normal skeletal muscle cells become cancerous. Because skeletal muscle cells are found in virtually every site of the body, RMS can develop in almost any part of the body.

The first description of RMS was by Weber in 1854. However, the "definitive" publication is usually considered to be by Stout in 1946, 92 years later.

  • Weber, CO. Anatomische Untersuchung Einer Hypertrophieschen Zunge nebst Bemekugen uber die Nubildung querquestreifter Muskelfsern, Virchow Arch. Pathol Anat. 7:115, 1854.
  • Stout AP: Rhabdomyosarcoma of the skeletal muscles, Ann Surg 1946; 123: 447-472.

Figure 1: Age at Diagnosis for children with RMS.

Figure 1: Age at Diagnosis for children with RMS...

RMS is a very rare cancer. There are only about 350 cases of RMS diagnosed each year in the United States in children under the age of 21 years. About four children per million healthy kids under the age of 15 will develop RMS each year. It is slightly more common in boys than in girls and it is most common in young children under the age of five.

Rhabdomyosarcoma is very uncommon in adults. There have been five "large" published series, totaling just over 400 cases of "adult" RMS (including some "children") seen at major cancer centers in the United States and Europe over the past 20-30 years.1-5 Although "pleomorphic" histology is more common in the adult population (and rarely seen in children), treatment principles for managing adults with RMS are similar to those for children, and outcome is not intrinsically worse for adults treated with "modern", multi-modality therapy.

Adult Cases

Rhabdomyosarcoma in AdultsTreatment principles for managing adults with RMS are similar to those for children. The five series mentioned above are from:

  1. Instituto Nazionale Tumori, Milan, Italy, 190 patients 18 years of age or older over a 25 year period,1
  2. Memorial Sloan-Kettering Cancer Center, New York City, NY, 84 patients 16 years of age or older over a 17 year period,2
  3. M.D. Anderson Cancer Center, Houston, TX, 82 patients 17 years of age or older over a 28 year period,3
  4. Dana-Farber Cancer Institute, Boston, MA, 39 patients 16 years of age or older over a 23 year period,4
  5. Armed Forces Institute of Pathology (Washington, D.C., 38 patients 21 years of age or older over a 30 year period, all with pleiomorphic RMS.5

They highlight several key points about "adult" RMS:

  1. They are as intrinsically responsive to chemotherapy as "pediatric" RMS with response rates to chemotherapy as high as 85%.
  2. "Unfavorable" histologies, including alveolar and pleiomorphic, are more common than embryonal histology.
  3. The proportion of patients with Group I, II, III, and IV tumors are comparable to that seen in "pediatric" seri.
  4. With appropriate treatment, even accounting for differences in the proportion of patients with "unfavorable" histologies, survival rates comparable to that seen in "pediatric" series can be achieved.

Although these tumors can arise almost anywhere, the most common locations for these tumors to develop are in the structures of the head and neck (nearly 40% of all cases), the male or female genitourinary tract (about 25% of all cases), and the extremities (about 20% of all cases).

Table 1: Incidence of RMS by site of primary tumor
GU (all)

Approximately 40% of newly diagnosed RMS arise in head and neck structures including parameningeal sites (16% of all cases, and almost half of all head and neck cases), the orbit or eyelid (10% of all cases), and other non-orbit, non-parameningeal sites (10% of all cases). Approximately 25% of cases arise in one of the structures of the genitourinary system including the paratesticular region, the female genitourinary tract (vulva, vagina, cervix, uterus), the urinary bladder, and the prostate. Approximately 20% of cases arise in an extremity. The remainder of cases ("other") arise in diverse sites including the chest wall and retroperitoneum.

Tumors that arise in the orbit, non-parameningeal head and neck sites (for example, the cheek or the ear lobe), and the male (paratesticular) or female (vagina, vulva, cervix, or uterus) genital tracts are considered "favorable." All other sites are considered "unfavorable."

Most children who develop RMS don’t have any clear risk factor for getting cancer. After taking a careful family history and doing a thorough physical examination, approximately one child in five to one child in ten will have an identifiable "genetic risk factor": the most common of these genetic "syndromes" include the Li-Fraumeni syndrome,6 neurofibromatosis,7 Beckwith-Wiedemann syndrome,8 and Costello syndrome.9

Genetic Risk Factors and Syndromes

Although the overwhelming majority of cases of RMS occur sporadically, between 10-33% of children who develop RMS are thought to have an underlying genetic risk factor.10 The development of RMS has been associated with a number of rare familial "cancer syndromes" such as the Li-Fraumeni syndrome (LFS), which includes familial clustering of RMS and other soft tissue tumors in children, with adrenocortical carcinoma and early-onset breast carcinoma in adult relatives. The LFS has been associated with germline mutations of the p53 tumor suppressor gene.11 One study of 33 cases of sporadic RMS, found that three of 13 children younger than three years of age at diagnosis (compared with none of the 20 children older than three years of age) had germline mutations in their p53 gene.12 RMS has also been seen in association with Beckwith-Wiedemann syndrome, a fetal overgrowth syndrome associated with abnormalities on 11p15, where the insulin-like growth factor II (IGFII) gene is located. Studies of children with Costello’s syndrome, likely an autosomal dominant disorder characterized by post natal growth retardation, typical coarse faces, loose skin and developmental delay, have noted an increased risk for development of solid tumors, most commonly rhabdomyosarcoma. There have been ten cases of RMS reported in approximately 100 known children with Costello syndrome.

Rhabdomyosarcoma Symptoms

The symptoms that are associated with RMS can vary widely depending on where the tumor develops. Children with orbital RMS (about 10% of all cases of RMS), may present with a bulging or swollen eye (proptosis). Although this can sometimes be mistaken for a sinus infection, children with tumors in this location usually do not have the other symptoms that children with sinus infections experience (pain, fever, purplish discoloration of the eye).

Case 1

Figure 2: Case 1: A 7-year old boy with orbital RMS.

Figure 2: Case 1: A 7-year old boy with orbital RMS...

A 7-year old boy presented with one week of swelling and pain of the left eye, without fever or purulent rhinorrhea. Intravenous antibiotics were administered for treatment of presumptive peri-orbital cellulitis. An MRI (shown below) was obtained and demonstrated an approximately four cm soft-tissue mass arising in the supero-medial aspect of the left orbit displacing the globe anteriorly and laterally. Biopsy of the mass was accomplished by a small, medially placed incision. The diagnosis of embryonal RMS was confirmed. No distant metastases were found on CT chest, bone scan, or bone marrow biopsy. The patient was Stage 1, Group III and was treated successfully with VA chemotherapy plus 45 Gy local XRT.

Children with tumors arising in the one of the parameningeal sites (basically the sinuses, the middle ear, and the back of the throat) may complain for weeks or months of a stuffy nose, sometimes with nasal discharge; occasionally, a mass may be visible in the nostril or the back of the throat. Unlike sinus and throat infections, these tumors usually don’t spread to the lymph nodes in the neck. If they do, they usually are non-tender. If erosion of the skull base occurs, they may complain of headache or develop cranial neuropathies from infiltration or compression of affected cranial nerves.

Case 2

Figure 3: Case 2 A 14-year old girl with parameningeal RMS.

Figure 3: Case 2 A 14-year old girl with parameningeal RMS...

A 14-year old girl presented with a two week history of rapidly worsening right-sided proptosis and "swollen glands" on the right side of her neck. MRI demonstrated a multi-compartmental nearly seven cm soft tissue mass (shown below) centered in the sinonasal cavity and extending through the cribriform plate into the anterior cranial fossa. No edema was seen within the frontal lobes to suggest direct parenchymal extension of the tumor. Multiple enlarged lymph nodes were also seen in the right lateral retropharyngeal region and in the right anterior cervical chain. Physical examination was notable for marked right-sided proptosis and ophthalmoplegia with preserved vision. A mass was visible in the right nares. Rock-hard cervical lymphadenopathy was present. A fine needle aspiration (FNA) of the cervical nodes revealed a small, round blue cell tumor suspicious for RMS. A biopsy of the mass in the nasal cavity demonstrated the characteristic "alveolar" appearance of alveolar RMS. Immunostains were strongly positive for desmin, vimentin, and myogenin. RT-PCR confirmed the presence of a t(2;13) PAX3-FKHR translocation. CSF cytology was negative for malignant cells. No evidence of distant metastases was found on CT chest, bone scan, PET scan, or bone marrow biopsy. A diagnosis of Stage 3, Group III alveolar RMS with a paramengingeal primary (likely the ethmoid sinus) with intracranial extension was made. All sites of initially visible tumor disappeared completely on follow-up MRI and PET scan following just two cycles of chemotherapy. Despite the administration of additional chemotherapy and full-dose (50.4 Gy) XRT to the primary site and all involved lymph nodes, rapidly progressive and ultimately fatal leptomeningeal recurrence was documented within the radiation field six months from the start of therapy.

Children with tumors arising in the genitourinary tract may present with a painless scrotal mass (paratesticular tumors), a protruding grape-like mass in the vagina ("botryoidal" rhabdomyosarcoma), blood in the urine (bladder tumors), or frequent urination, sometimes with burning or hesitancy. Occasionally, tumors that arise in the prostate gland (not the same as the more common type of prostate cancer that adult men get) can grow very large before they are diagnosed; these tumors may present as a visible mass in the pelvis or abdomen, sometimes with urinary frequency and urgency, sometimes with constipation, nausea and vomiting from compression of the bowels.

Case 3

Figure 4: Case 3: An 18-year old man with prostate RMS.

Figure 4: Case 3: An 18-year old man with prostate RMS...

An 18-year old college student developed erectile dysfunction, acute abdominal pain, right-sided flank pain, urinary frequency, hesitation, and decreased stream. Oral antibiotics were administered without improvement. A CT scan demonstrated a 10 x 6.5 x 7.3 cm pelvic mass arising in the vicinity of the prostate, inseparable from the posterior wall of the bladder and anterior wall of the rectum, obstructing the right ureter and causing right hydronephrosis, with associated bilateral external and left internal iliac adenopathy. Similar findings were seen on MRI (shown below). A transrectal needle biopsy yielded material that was comprised of a densely cellular small round blue cell tumor, strongly positive for desmin, vimentin, actin, and myogenin on immunostaining, and containing a t(2;13) PAX3-FKHR translocation on RT-PCR. A temporary percutaneous nephrostomy tube was placed to relieve the right-sided hydronephrosis. No distant metastases were seen on CT chest, bone scan, or bone marrow biopsy. A diagnosis of Stage 3, Group III alveolar RMS of the prostate was made and aggressive, multi-agent chemotherapy was commenced to which the patient achieved a complete response. Erectile function returned to normal. Additional chemotherapy and full-dose (50.4 Gy) pelvic XRT was administered; treatment was complicated by the development of hemorrhagic cystitis and radiation enteritis. The patient returned to college less than three months after the completion of eight months of treatment and remains in continuous complete remission 18 months from diagnosis.

Tumors that arise in the legs or arms are usually amongst the most aggressive types of RMS. These tumors may grow from the size of a mosquito bite or a small marble to the size of a baseball or grapefruit in the course of only a few weeks. The tumors are usually hard, but only rarely are they painful unless they start pressing on nearby nerves. These tumors are the most likely to spread to nearby lymph nodes; it is not uncommon for a child with a RMS in the hand or arm to also have "swollen glands" in the armpit, or for a child with a RMS in the foot or calf to also have "swollen glands" in the groin.

Case 4

Figure 5

Figure 5

A 7-year old boy was found to have a firm, painless "lump" in his left calf while being bathed. Physical examination confirmed a rock-hard mass in the calf with obviously enlarged lymph nodes in the popliteal and inguinal regions. MRI demonstrated a large soft-tissue mass in the calf with evidence of hemorrhage (shown), extending cephalad through the popliteal fossa. CT scan of the chest abdomen and pelvis demonstrated the presence of inguinal and pelvic lymphadenopathy, and "suspicious" para-aortic lymphadenopathy; PET scan confirmed that these nodes were hypermetabolic, consistent with metastases. An incisional biopsy of the calf mass and inguinal node demonstrated a "classic" alveolar RMS; RT-PCR confirmed the presence of a "consensus" PAX-FKHR translocation. Except for the nodal metastases, no other distant metastases were found in the lung, bones, or bone marrow. A diagnosis of Stage 4, Group IV alveolar RMS of the extremity with regional (popliteal and inguinal) and distant (pelvic and para-aortic) nodal metastases was made. Within one week of starting chemotherapy, the calf tumor had shrunk by more than 50% and the hypermetabolic nodal disease had resolved. Treatment is ongoing on a MSKCC single-institutional pilot protocol for "high-risk" patients.

Occasionally, children with RMS will also have unexplained fevers as one of the symptoms that are noticed at the time of diagnosis. Appetite may or may not be depressed. Fatigue and easy bruising are relatively uncommon symptoms unless the tumor has spread to the bone marrow.

Prognostic Factors

Although RMS is considered one disease, there are important differences in how these tumors behave depending on where they arise in the body, how they look under the microscope, how big the tumor is and whether it has spread anywhere, how much of the tumor remains after the initial operation, and the patient’s age at the time of diagnosis. These are called "prognostic factors." They describe "statistical probabilities" for cure but are never able to determine whether an individual child, regardless of how "favorable" or "unfavorable" her prognostic factors, will be cured.

Risk-Stratisfied Therapy

The following table summarizes how the combination of site, tumor size, regional nodal status, distant metastases, age at diagnosis, and histology is used to generate risk-stratified therapy for patients with RMS. The Column entitled "Risk" stratifies patients into one of four risk group (Low-A, Low-B, Intermediate, and High) that is used to assign the appropriate treatment on the Fifth Intergroup Rhabdomyosarcoma Study (IRS-V). The specific protocol number is indicated in the parentheses as the letter "D" followed by a four-digit figure.

D9602 is the "low-risk" study consisting of approximately eleven months of chemotherapy treatment on either Arm A (2-drug chemotherapy with vincristine plus dactinomycin [VA], with or without radiation therapy) or Arm B (3-drug chemotherapy with vincristine plus dactinomycin plus cyclophosphamide [VAC], with radiation for almost all patients); D9803 is the "intermediate-risk" study consisting of a randomization between chemotherapy according to Arm A (14 cycles of VAC) or Arm B (eight cycles of VAC alternating with six cycles of vincristine plus topotecan plus cyclophosphamide), plus radiation therapy; D9802 is the "high-risk" study consisting of a "phase II window" with irinotecan administered on the "daily x 5 x 2 schedule" developed in the Houghton lab at St. Jude Children’s Research Center.13 either as a single-agent or in combination with vincristine, followed by either eight cycles of VAC plus four cycles of vincristine plus irinotecan for patients responding to irinotecan, or 12 cycles of VAC chemotherapy for patients not responding to irinotecan, plus radiation therapy. The various IRS-V studies are expected to complete accrual by the end of 2004. Successor studies are planned to open in 2005-2006.

Rhabdomyosarcoma Risk Group Definitions

Favorable = Orbit/eye lid, head and neck (excluding parameningeal), genito-urinary (not bladder or prostate)
Unfavorable = Bladder, prostate, extremity, parameningeal, other (trunk, retroperitoneal, etc)
a = Tumor size <= Five cm in diameter
b = Tumor size > Five cm in diameter
EMB = Embryonal, botryoid or spindle variants or ectomesenchymomas with embryonal features
ALV = Alveolar or undifferentiated sarcomas, or ectomesenchymomas with alveolar features
N0 = Regional nodes not clinically involved
N1 = Regional nodes clinically involved
NX = Node status unknown

Table 2: Risk-stratification for patients with newly diagnosed RMS
Risk Stage Group Site Size Age Histology Metastasis Nodes
Low A (D9602) 1 I favorable

a or b

<21 EMB M0 N0 or N1 or NX
1 II favorable a or b <21 EMB M0 N0 or NX
1 III orbit only a or b <21 EMB M0 N0 or NX
2 I unfavorable a <21 EMB M0 N0 or NX
Low B (D9602) 1 II favorable a or b <21 EMB M0 N1
1 III orbit only a or b <21 EMB M0 N1
1 III favorable (excluding orbit) a or b <21 EMB M0 N0 or N1 or NX
2 II unfavorable a <21 EMB M0 N0 or NX
3 I or II unfavorable a <21 EMB M0 N1
3 I or II unfavorable a <21 EMB M0 N0 or N1 or NX
Intermediate (D9803) 2 III unfavorable a <21 EMB M0 N0 or NX
3 III unfavorable a <21 EMB M0 N1
3 III unfavorable b <21 EMB M0 N0 or N1 or NX
1 or 2 or 3 I or II or III favorable or unfavorable a or b <21 ALV M0 N0 or N1 or NX
4 IV favorable or unfavorable a or b <10 EMB M1 N0 or N1 or NX
High (D9802) 4 IV favorable or unfavorable a or b >=10 EMB M1 N0 or N1 or NX
4 IV favorable or unfavorable a or b <21 ALV M1 N0 or N1 or NX

Oncologists use a special set of short-hand terms to describe these factors. For children with RMS, there are two sets of terminology that are used to describe these factors. One is called Stage and the other is called Clinical Group (or "Group" for short). The Stage of RMS is dependent upon three factors:

  1. What part of the body the tumor arose in
  2. How big the tumor is
  3. Whether or not the tumor has spread (see below) regionally or distantly

The Group of RMS is dependent upon how much tumor is still present after the initial surgery. There are four Stages (Stage 1, 2, 3, and 4) and four Groups (Groups I, II, III, and IV). Each patient with RMS is assigned a Stage and a Group based upon the combination of these factors.

Staging System

The following tables contain the detailed site-modified TNM staging system and surgico-pathologic Clinical Group system used to categorize patients with RMS. These "short-hand" systems are one of the more confusing aspects of caring for children with RMS. Any tumor that arises in one of the favorable locations is Stage 1 as long as it has not visibly spread to another "distant" part of the body (see below). Any tumor that has visibly spread to another "distant" part of the body is always Stage 4. Tumors that arise in any of the unfavorable locations will either be Stage 2 (if they are "small" and have not spread to the lymph nodes) or Stage 3 (if they are "big" or have spread to the lymph nodes). Most children with RMS have Stage 2 or Stage 3 tumors. Since the TNM "staging" system does not require pathologic confirmation of imaging abnormalities, problems with accurately classifying patients can arise when, for example, a patient would be Stage 4 based on the presence of a pulmonary nodule on CT scan that is believed to represent a metastasis but is then found to not contain tumor when surgery is done to remove it.

Table 3: Site-modified Tumor, Nodes, Metastasis (TNM) Staging System for patients with newly diagnosed RMS
Stage Site T Status Size Node Status Metastasis
1 Favorable T1 or T2 a or b N0, N1, or NX M0
2 Unfavorable T1 or T2 a N0 or NX M0
3 Unfavorable T1 or T2 a N1 M0
3 Unfavorable T1 or T2 b N0, N1, or NX M0
4 Favorable or Unfavorable T1 or T2 a or b N0 or N1 M1

Any tumor that is completely removed at the time of the initial operation is Group I. A tumor that has visibly spread to another "distant" part of the body is always Group IV. A tumor that is still visible (on scans or on physical examination) after the initial operation is Group III. Group II is when all of the visible tumor is removed but there is still "microscopic" amounts of tumor cells left behind - with or without spread to the regional nodes (as long as they are also removed). Half of all children with RMS have Group III tumors.

Table 4: Intergroup Rhabdomyosarcoma Group (IRSG) Clinical Group staging system for patients with newly diagnosed RMS
Clinical Group Definition
I Complete resection, (-) margins
IIa Complete resection, (+) margins
IIb Complete resection, (-) margins resected nodes positive
IIc Complete resection, (+) margins resected nodes positive
III Gross residual disease (includes unresected regional nodes)
IV Distant metastases

Patterns of Spread

RMS can spread locally, regionally, or distantly.

  1. Local spread means that the tumor infiltrates or invades the tissues in the immediate vicinity of where it started.
  2. Regional spread means that the tumor has traveled to the lymph nodes that drain the area where it arose. The highest chance that RMS will spread to the lymph nodes is for children with tumors that arise in the extremities and in older boys (ten years of age or older) with paratesticular tumors.
  3. Distant spread means that the tumor has traveled through the bloodstream to another part of the body. The most common places that RMS travels to are the lungs, bones, and bone marrow.

It is very uncommon for RMS to spread to the brain or other organs such as the liver or spleen. When tumors have spread visibly to a "distant" location they are called "metastases." Only about one child in five with RMS will have distant metastases.

A variety of different tests are needed to evaluate the primary tumor and to look for signs that it may have spread to other parts of the body. The first test is always a thorough history and physical examination. Generally, the best imaging test to evaluate the primary tumor is a MRI. This provides 3-dimensional imaging and is frequently helpful for the purposes of planning radiation or surgery. CT scans of the chest are routinely done to look for the possibility of tumor having "metastasized" to the lungs. Depending on the location of the primary tumor, CT scans of the abdomen and pelvis are sometimes also done to look for spread of the tumor to lymph nodes. A bone scan is a nuclear medicine test that looks at the entire skeleton to determine if the tumor might have spread to the bones. Another nuclear medicine test that is being utilized increasingly is called a PET scan (Positron Emission Tomography). This test is relatively unique in that it images the entire body, both bones and soft tissues, can often be used to clarify an ambiguous finding on CT or MRI and can also be used to assess response to treatment. Because RMS can spread to the bone marrow, patients with RMS also undergo bone marrow aspirates and biopsies; a needle is placed into the hip bones and a specimen of the bone marrow is removed for testing; these tests are almost always done at the same time that anesthesia is being given for the biopsy of the tumor or insertion of the central venous catheter (CVC). Patients with tumors arising in one of the parameningeal locations must always have a lumbar puncture ("spinal tap") performed to obtain a sample of their cerebrospinal fluid (CSF) for testing to make sure that the lining of the brain has not become infiltrated by RMS.


Approximately 20% of newly diagnosed patients will present with one or more sites of "distant" metastases. A disproportionate number of these patients will have alveolar histology tumors. Of 127 patients with metastatic RMS treated on IRS-IV, 46% of patients had alveolar tumors compared to 22% of the nearly 900 patients with non-metastatic tumors treated on IRS-IV.14 Nearly 60% of patients had metastases confined to one location; the commonest site of metastatic spread was the lungs, followed by the bone marrow, lymph node, and bones. Although bone marrow aspirations and biopsies are routinely recommended as part of the staging evaluation of patients with known or suspected newly diagnosed RMS, isolated bone marrow involvement was found in only 12 of 900 patients without other sites of known metastases; thus, the "yield" of bone marrow aspiration and biopsy in patients with otherwise localized RMS is less than 2%.

General Principles of Rhabdomyosarcoma Treatment

All children with RMS are treated with chemotherapy. Depending upon the size and location of the primary tumor, and how much of it can be surgically removed, most children will also receive some combination of radiation therapy and surgery.


The diagnosis of RMS can never be made without obtaining a specimen of the tumor for testing in the laboratory. The initial process for obtaining this specimen is called a biopsy. A biopsy is usually considered a "small" operation; most of the time it does not require an overnight stay in the hospital. There are different ways that a specimen of the tumor can be obtained:

  1. A percutaneous needle biopsy: in this procedure, a needle is placed through the skin into the tumor and a small piece of the tumor is removed inside the needle. Sometimes this procedure is done using an ultrasound or CT scan to guide the person doing the biopsy. This procedure is usually not done with anesthesia, although intravenous sedation may be required depending on the site of the tumor and age of the child. Depending on the location of the tumor, this procedure may or may not be safer than one of the procedures discussed below. A needle biopsy is able to provide an adequate specimen to make a correct diagnosis about 90% of the time.
  2. An open incisional biopsy: in this procedure, which is almost always done under anesthesia, a small cut is made in the skin through which a small piece of the tumor is removed. This procedure provides an adequate specimen to make a correct diagnosis about 100% of the time.
  3. An open excisional biopsy: in this procedure, which is almost always done under anesthesia, a cut is made in the skin and an attempt is made to remove the entire tumor. This is a bigger operation than either of the two other procedures. This operation is appropriate for children whose tumors have been fully imaged if the surgeon believes that the entire tumor can be removed and doing so will not result in either a functional deficit (that is, if a calf tumor could be taken out without doing an amputation or otherwise compromising the ability to ambulate) OR a cosmetic defect (that is, if a tumor of the sinuses could be taken out without producing a big facial scar or facial deformity).

Because imaging studies can fail to detect many instances of tumor spread to regional lymph nodes, surgical evaluation of regional nodes is mandatory in two specific cases, children with extremity RMS and boys ten years of age or older with paratesticular tumors. In the former instance, surgical sampling of lymph nodes behind the knee or in the groin should be performed for lower extremity tumors, and sampling of lymph nodes behind the elbow or in the armpit should be performed for upper extremity tumors.15 The role of lymphoscintigraphy for identifying a sentinel node is under investigation. PET scanning may be helpful at identifying worrisome nodes not otherwise clearly seen on conventional imaging such as CT or MRI.

In the case of boys with paratesticular tumors, and ideally at the same time that the primary tumor is removed (an inguinal incision should be performed, as would be done for a hernia operation, and the tumor and testicle should both be extracted in contiguity from the scrotal sac and resected), surgical evaluation of ipsilateral (same side as the tumor) retroperitoneal regional lymph nodes should be performed; this latter procedure is increasingly being done laparoscopically, minimizing post-operative recovery and potentially shortening the time until chemotherapy is able to be initiated.16

It is important to remember that surgery by itself is never curative for children with RMS. It is also important to remember that the role of surgery is very dependent on the site of the tumor. While initial complete surgical removal of tumors arising in an extremity or in the pelvis may help improve the chance of cure, complete removal of a tumor arising in the orbit or vagina is almost never necessary to achieve a very high rate of cure (and is almost never appropriate). Although most families whose child is suspected of having RMS want the whole tumor taken out as quickly as possible, this initial surgical procedure is almost never an emergency and it is imperative that proper imaging of the tumor be obtained before a biopsy is performed if RMS is being considered. Failure to image the primary tumor before a biopsy can result in an irreversible loss of opportunity to properly plan critically needed radiation therapy. Similarly, it is important to ensure that the biopsy is obtained at a facility with experienced pathologists who will process the specimen in the appropriate fashion to ensure that all necessary testing is performed in a timely and thorough manner.17


Figure 6: Microscopic appearance of Embryonal RMS.

Figure 6: Microscopic appearance of Embryonal RMS...

Once biopsied, the tumor is studied under the microscope in the laboratory. The defining characteristic of RMS is the demonstration of evidence of skeletal muscle lineage—either by its appearance under the microscope or by the pattern of chemical staining ("immunostaining"). There are two basic kinds of RMS – embryonal and alveolar. Approximately two-thirds of children with RMS have the more common embryonal type (or the spindle-cell or botryoid variants). These tumors are more common in younger children, particularly those with tumors arising in the head and neck sites (including parameningeal sites) and the genitourinary system (including the bladder and prostate). The tumor cells tend to be more elongated and less densely cellular.

Figure 7: Microscopic appearance of Alveolar RMS.

Figure 7: Microscopic appearance of Alveolar RMS...

About 20-25% of children with RMS have the less common alveolar type (or solid alveolar variant). These tumors are much more common in teenagers, and most commonly arise in the extremities. The tumor cells tend to be smaller and rounder, often with a denser cellularity, and are so named because of their resemblance to the appearance of the small air sacs in the lungs (the "alveoli"). Alveolar tumors are often considered more "aggressive", or "higher risk", than embryonal tumors – particularly for tumors that arise in one of the favorable locations.

About 5-10% of children will have tumors that cannot be more definitively categorized and are considered either "undifferentiated" sarcomas or "rhabdomyosarcoma, not otherwise specified."

When a tumor has been biopsied and the pathologist (the doctor who studies the tumor in the laboratory) suspects that it is RMS, she will usually order confirmatory tests called "immunostains." These are chemical reactions that stain different structures in the tumor cell. RMS tumors will usually stain "positively" for a number of different stains including desmin and myogenin. The demonstration of myogenin positivity is virtually diagnostic of RMS.

Figure 8: Over-expression of Insulin-Like Growth Factor Type II (IGF-II).

Figure 8: Over-expression of Insulin-Like Growth Factor Type II (IGF-II)...

A final level of testing is sometimes done on RMS tumor cells. This is called "molecular diagnostic testing." Although not much is known about why a normal skeletal muscle cell becomes cancerous, there is quite a lot known about the genetic changes that occur in the cell once it does become a cancer cell. In virtually all cases of embryonal RMS, an abnormality can be found in the cancer cells (and only in the cancer cells – so this is not an inherited abnormality!) that causes an "over-dosage" of a gene that is important in the growth of normal muscle cells.

Cases of embryonal RMS typically demonstrate evidence of over-expression of the IGF-II gene located on the short arm of chromosome 11. This is believed to result from loss of the maternal allele and duplication of the paternal allele. It is thought that the expression of two copies of this gene leads to an "overdose" effect whereby too much IGF-II produces a constant proliferative signal that allows the pre-cancerous (or already transformed) muscle cell to grow in an unrestrained fashion and prevents it from dying in response to what would otherwise be lethal environmental stresses. This process is known as "loss of heterozygosity."

Figure 9: Reciprocal translocation between PAX and FKHR creates a hybrid oncogene.

Figure 9: Reciprocal translocation between PAX and FKHR creates a hybrid 'oncogene'..

This process results in an "overdosage" of a "growth promoting gene", insulin-like growth factor Type II (IGF-II), that is located on chromosome 11. Normally, only one copy (usually the gene that is inherited from the father) of this gene is "active" and the other is "silent" (it’s believed that a chemical modification of the DNA structure near the gene, known as "methylation" is responsible for one gene being "on" and another nearby growth suppressing gene [H19] being "off"). In most cases of embryonal RMS, either both genes are activated or the copy of the mother’s gene is lost and the father’s gene is duplicated and both copies are "active." This is thought to lead to the production of a constant "proliferative" signal that tells the cell to continue to grow and prevents it from dying in response to the normal environmental stresses that cells face.

Many cases of childhood cancer are associated with specific translocations whereby a piece of one normal gene and a piece of another normal gene break apart and switch places. In approximately 90% of cases of alveolar RMS, a portion of one of the PAX genes (most commonly the PAX 3 gene located on chromosome 2, less commonly the PAX 7 gene located on chromosome 1) fuses with a portion of the FKHR gene (located on chromosome 13) to create a new "hybrid" gene (PAX-FKHR) that turns on growth-stimulatory genes that would otherwise be "inactive" and turns off growth-inhibitory genes that are normally active. Since this abnormal "hybrid" gene is found only in cases of alveolar RMS, it can be used for diagnostic purposes and, potentially in the future, as a target for immune-mediated cancer therapies.

This abnormality can often be detected using one of several specialized techniques for looking at the chromosomal content of the tumor cells.

Nearly 90% of cases of alveolar RMS will have a characteristic "translocation" involving one of the "PAX" genes (most commonly the PAX 3 gene, located on chromosome 2, less commonly the PAX 7 gene, located on chromosome 1) and the "forkhead" (FKHR) gene (located on chromosome 13).

A translocation is a fairly common "event" in childhood cancers in which a piece of a normal gene breaks away from its usual location and joins a piece of another normal gene. Specifically, by fusing the "paired box" (PB) and "homeodomain" (HD) DNA binding regions of the PAX 3 gene with the "transcriptional activation domain" (TAD) of the FKHR gene, a new "hybrid" gene is created that appears to play a critical role in the process by which the RMS cell becomes cancerous in two ways. First, it turns "off" other genes that are normally "active" and serve as "brakes" on cell growth; and, second, it turns "on" other genes that are normally "inactive" and serve as stimulators of cell growth, survival, and spread. This abnormality is never seen in embryonal RMS so if there is a question about which type of RMS a patient has based on how it looks under the microscope, the demonstration of a PAX-FKHR translocation proves conclusively that it is alveolar RMS. This abnormality is usually tested for using a technique known as RT-PCR (reverse transcriptase polymerase chain reaction), however, this test may only be available in specialized reference laboratories at large Cancer Centers or Children’s Hospitals.


The two major histologic subtypes of RMS, namely embryonal and alveolar, have been found to have characteristic but distinct genetic alterations that are presumed to play a role in the pathogenesis of these tumors. Alveolar RMS has been demonstrated to have a characteristic translocation between the long arm of chromosome 2 and the long arm of chromosome 13, referred to in shorthand notation as t(2;13)(q35;q14).18-19 This translocation has been molecularly cloned and has been shown to involve the juxtaposition of the PAX3 gene (or, rarely, the PAX7 gene located at chromosome 1p36), believed to regulate transcription during early neuromuscular development, and the FKHR gene, also known as FOXO1a, a member of the forkhead family of transcription factors.20-21 It is presumed that the consequence of this fusion transcription factor is the abnormal activation of transcription from a gene or genes that contribute to the transformed phenotype. Although the precise consequence of this tumor-specific translocation remains to be elucidated, it has been shown using cDNA microarray analysis that the PAX-FKHR fusion expressed in fibroblasts specifically turns on an array of myogenic factors.22 Furthermore, PAX-3-FKHR has been found to upregulate c-MET expression, a receptor tyrosine kinase that has been implicated in transformation.23 The use of polymerase chain reaction (PCR) for precise confirmation of the diagnosis of alveolar RMS based on genetics is likely to become more widely used in the near future. Recently, a novel amplicon has been identified at 13q31 in approximately 20% of cases of ARMS suggesting that one or more genes at this locus contribute to the pathogenesis of these tumors.24

The other major histologic subtype, embryonal RMS, is known to have loss of heterozygosity (LOH) at the 11p15 locus.25-26 Furthermore, it has been shown that this LOH involves loss of maternal genetic information with duplication of paternal genetic material at this locus.27 This region is of particular interest because it is the location of the IGFII gene, which codes for a growth factor believed to play a role in the pathogenesis of RMS (see later discussion). IGFII has been demonstrated to be imprinted with only the paternal allele being transcriptionally active.28-29 It is therefore conceivable that in this tumor, LOH with paternal disomy may lead to overexpression of IGFII. However, it is also possible that LOH at 11p15 may reflect the loss of a tumor suppressor activity that has not been identified, or that both activation of IGFII and loss of tumor suppressor activity result from LOH at 11p15 in embryonal RMS.30

Several investigators have recently reported findings using comparative genomic hybridization (CGH) analysis of RMS tumors and cell lines. Three features standout. Firstly, regions of genomic amplifications are seen in ARMS and anaplastic ERMS, suggesting that these subtypes share similar genetic events.31 Secondly, several studies have noted significant amplification of 15q25-26, the locus for the IGFI receptor24,31 and specific IGFI R amplification was confirmed by PCR and FISH.31 This is of particular note since IGF signaling is implicated in RMS. Finally, two studies have demonstrated loss at 9q22 in approximately 33% of tumors. This region corresponds to the PTH locus, a tumor suppressor gene implicated in RMS development in a mouse model of Gorlin syndrome.31-32

Once all of the imaging studies have been completed, and the biopsy has been performed, and the diagnosis of RMS has been confirmed, it is possible to classify patients with RMS into one of four "risk groups" based on the combination of their Stage (site, size, nodal involvement), their Group (extent of residual tumor post-operatively), their age at diagnosis, their histologic sub-type (embryonal versus alveolar), and the presence or absence of distant metastases. These risk groups provide important information about the potential curability of the tumor with treatments of lesser or greater intensity:

  1. Standard-risk, subgroup A: These patients, relatively few in number, have a survival of better than 85% using relatively non-intensive, 2-drug chemotherapy, with or without radiation therapy. This group is essentially comprised of patients with orbital tumors (as long as they have not metastasized), patients with "favorable" site tumors (Stage 1) that have been either completely removed surgically (Group I) or gross totally removed with only microscopic residual disease (Group II), and patients with small unfavorable site tumors (Stage 2) that have been completely resected (Group I).
  2. Standard-risk, subgroup B: These patients, slightly more numerous, have a survival of better than 80% but need relatively more intensive, 3-drug chemotherapy, usually with radiation therapy (with one important exception, see below). This group is comprised of all patients with non-metastatic, non-orbital favorable site tumors (Stage 1) that are still visible (Group III) after initial surgery, patients with non-metastatic, small unfavorable site tumors without regional nodal spread (Stage 2) that have been gross totally resected (Group II), and patients with unfavorable site tumors that are large or have spread to regional nodes (Stage 3) but have been completely or gross totally resected (Groups I and II). Approximately 15-20% of all newly diagnosed RMS patients will be considered "standard-risk." Patients with alveolar RMS are never considered standard-risk.
  3. Intermediate-risk: These patients comprise the majority of patients with newly diagnosed RMS and include those with unfavorable site tumors (Stages 2 and 3) that have not been completely resected (Group III), patients under the age of ten with embryonal RMS that has spread to other parts of the body (Stage 4, Group IV), and all patients with non-metastatic alveolar RMS. Although this is a diverse group of patients, the prognosis for cure with 3 (or more) drug chemotherapy and radiation therapy is usually better than 50%, and perhaps as high as 70% for certain sub-groups.
  4. High-risk: These patients comprise approximately 10-15% of patients with newly diagnosed RMS. The prognosis for cure for these children is usually quite poor, generally between 20% and 35%, even with very aggressive chemotherapy, radiation, and surgery. This group includes all patients with metastatic alveolar RMS, patients ten years of age or older with metastatic embryonal RMS, and probably two other groups currently considered intermediate-risk: infants under one year of age with metastatic embryonal RMS, for whom the 5-year survival is less than 20%,33 and children with extremity tumors with regional nodal spread, almost all of whom have alveolar RMS, for whom the 5-year survival is approximately 30%.15

Rhabdomyosarcoma Treatment

The treatment of patients with RMS is multi-disciplinary and begins even before the start of treatment with the availability of skilled radiologists who can accurately interpret the results of imaging studies, skilled pathologists who are familiar with the evaluation and testing of pediatric "small round blue cell tumors", and skilled surgeons who understand the role of initial surgery in the overall management of patients with RMS. It includes radiation oncologists and pediatric oncologists who are familiar with national (or institutional) treatment guidelines (also known as protocols) for treating this rare form of cancer. Ideally, treatment will be given at a facility where regular meetings of all of these disciplines (known as Tumor Boards) are held so that all of the health care providers involved in the child’s care can see the important imaging tests, biopsy results, and on-treatment evaluations that are necessary to give optimal care.

Given the young age of these patients, the treatment team should also include anesthesiologists to sedate patients for scans and procedures (including sometimes for the entire 5-6 week course of radiation treatment), and nursing staff familiar with the unique medical needs and complications of children with cancer. Finally, it includes Social Work, Chaplaincy, and Child Life staff to help a family (and child) whose world has been shattered by the words "your child has cancer."

Treatment for children with RMS focuses on achieving "local control" and "systemic control." Local control refers to the permanent eradication of the "primary tumor." This is usually accomplished by surgical removal or irradiation of the tumor (or both) and any involved nearby areas, in addition to chemotherapy treatment. Systemic control refers to the permanent control of invisible "micrometastases" or visible "metastases", generally by chemotherapy (sometimes with additional surgery or radiation therapy). The risk that treatment will fail to be curative varies by "risk group." For most children with non-metastatic tumors (that is, Standard and Intermediate Risk), the greatest risk is that the primary tumor will not be permanently controlled. More than half of all treatment failures in these groups are "loco-regional" (that is, at or near the primary site). Failure to control the primary tumor is associated with a markedly increased risk of relapse at other parts of the body; this is probably a reflection of intrinsic or early-acquisition of resistance to chemotherapy and radiation therapy. For most children with metastatic tumors (that is, High Risk), the overwhelmingly greater risk of treatment failures is that the metastases will not be controlled even if the primary tumor is controlled. Although there are exceptions, because post-relapse survival is poor for the vast majority of children with recurrent RMS (less than 20% of patients who relapse will be cured), it is critical that optimal therapy be given at the time of diagnosis.


Treatment of most children with RMS is administered either on a cooperative group or single-institution or limited-institution clinical trial, or following the guidelines of the appropriate trial. Since 1972, the Intergroup Rhabdomyosarcoma Study Group (IRSG) has completed four large, sequential, prospective clinical trials treating over 4000 patients with RMS. For patients with non-metastatic tumors, the most recently completed study, IRS-IV, asked two major "research" (randomized) questions:

1. Would replacement of cyclophosphamide by ifosfamide (VAI), or dactinomycin by etoposide (VIE) improve outcome for children with Group III tumors compared to standard VAC chemotherapy?

2. Would hyperfractionated radiation (5940 cGy in twice daily fractions of 110 cGy) improve local control compared to conventional radiation (5040 cGy in daily fractions of 180 cGy)?

For patients with metastatic tumors, the most recently completed trial attempted to evaluate the anti-tumor activity and ultimate treatment efficacy of one of three two-drug pairs (ifosfamide plus doxorubicin, vincristine plus melphalan, and ifosfamide plus etoposide) added to "conventional" VAC chemotherapy.

The results of these studies have been published over the past several years.14,34-38 For children with non-metastatic tumors, no difference in outcome was seen between any of the three arms: VIE, VAI, VAC.35 On this basis, VAC chemotherapy continued to be recommended by the IRSG as the "gold standard" for children with RMS. Compared to the prior study, IRS-III, outcome was improved for only a small number of children with embryonal tumors, those with unresected (Group III) tumors arising in "favorable" locations, and those with completely or gross totally resected (Groups I and II) tumors arising in "unfavorable sites" (Stages 2 and 3).34 Overall 3-year failure-free survival [FFS] for the entire group of patients was 77%; patients with alveolar histology fared significantly worse (66% 3-year FFS versus 83% for patients with embryonal tumors). Hyperfractionated radiation therapy did not produce superior rates of local control (or have any impact on overall survival) compared to conventionally fractionated therapy.36 The overall rate of local control was 87%. The greatest risk of local treatment failure (local recurrence) was seen in patients with bladder/prostate (19%) and parameningeal (16%) tumors.

For patients with metastases, while all 3 drug pairs were highly active with response rates of between 60-80%,37-38 outcome remained poor. Overall survival for the entire group was less than 30%; there was a suggestion of better outcome in patients receiving IE in addition to VAC.38 The use of melphalan was found to be associated with impaired tolerability of subsequent chemotherapy. Although the outcome for patients with metastatic RMS remains poor, no benefit has been found to consolidation with high-dose chemotherapy and autologous bone marrow rescue.39


All patients with RMS require chemotherapy to maximize the chance for cure. Most children in the United States are treated on (or following) an International Clinical Trial formerly known as the "Intergroup Rhabdomyosarcoma Study" (now known as the Soft Tissue Sarcoma Committee of the Children’s Oncology Group). Over the past 30 years, four Intergroup Rhabdomyosarcoma Studies have been completed with over 4000 patients with RMS treated. The 5th generation of these studies will complete accrual this year. For select patients, usually those with Intermediate or High-Risk RMS, treatment on a "pilot" single- or limited-institution clinical trial may be available.

Chemotherapy treatments for RMS are always given through an intravenous line; generally, a special type of "permanent" intravenous line is placed prior to the start of treatment. Most patients with RMS receive chemotherapy treatments lasting 6-12 months (rarely longer, although depending on the severity of side effects, treatment that is scheduled to last ten months can sometimes last 15 months). Chemotherapy is generally given in two to five (or sometimes ten) day "pulses" or "cycles" every 3-four weeks. Some chemotherapy drugs can be given on a weekly basis.

Chemotherapy side effects can be "drug-specific" (that is, only seen with one or two drugs) or "general" (that is, seen with many drugs). The following is a list of the most common drugs that are used to treat RMS in the United States and in Europe:

Common side effects that may be seen (to lesser or greater degrees) with virtually all of the chemotherapy drugs that are used to treat RMS include hair loss, nausea and vomiting, loss of appetite, fatigue, mouth sores, and the development of low-blood cell counts. These side effects typically develop because of the effects of chemotherapy on rapidly dividing cells. While tumor cells are usually the most rapidly dividing cells in the body, other normal cells, such as hair cells, "mucosal cells" (the cells that line the mouth and intestines), and blood cells, are also rapidly dividing. Fortunately, there is usually a greater supply of these normal cells than of tumor cells so these side effects are usually temporary.

The development of low blood cell counts is the side effect that most limits the ability to give chemotherapy all the time (the way an infection would be treated) and is one of the most dangerous side effects. There are three major kinds of blood cells: red blood cells, white blood cells, and platelets. Typically, about seven or eight days from the start of a "cycle" of chemotherapy, the blood cells drop to very low levels and may remain low for 5-10 days. Red blood cells carry oxygen from the lungs throughout the body; when the red blood cell count is low this is called anemia and may produce fatigue. White blood cells are the body’s infection fighting cells; when the white blood cell count is low this is called leukopenia and may increase greatly the risk of developing a serious infection from the "germs" that are already in/on one’s own body. When the most important infection-fighting white blood cell count is low, this condition is called neutropenia. Platelets are the cells that help the blood to clot; when the platelet count is low, this increases the risk of bleeding, either spontaneously or from a cut. When the red blood cell count is low, a transfusion can be given to help improve fatigue; when the platelets are low, a transfusion can be given to reduce the risk of bleeding. Most children with RMS, even those with Standard-Risk, Subgroup A tumors who receive relatively less-intensive 2-drug chemotherapy with vincristine and dactinomycin, will require transfusion support with red blood cells and/or platelets at some point during their treatment. The one type of blood cell that can’t be transfused is the infection-fighting white blood cell; however, a medicine (G-CSF, filgrastim, Neupogen®) is available that can help the white blood cells return to a safe level more quickly.

Inflammation of the liver, though an uncommon side effect, can occur and can be life-threatening, particularly in very young children, and requires a heightened level of awareness to monitor and evaluate promptly laboratory tests of "liver function."

Though uncommon, the development of chemotherapy-induced "hepatopathy" can be a life-threatening complication. This condition is characterized by hyperbilirubinemia, ascites, coagulopathy, and reversal of flow in the portal vein on Doppler ultrasound. Age less than three years increases the risk. Age-based chemotherapy dose modifications may reduce the risk of hepatopathy, particularly in young children.40

Vincristine is a drug that is given to virtually all children with RMS. Uniquely, it can cause pain in the hands and feet or in the jaw or abdomen. It can also produce weakness in the hands and feet due to (usually reversible) nerve damage (peripheral neuropathy). Presently, there are no proven "protective" medications to prevent this nerve damage, but there is some evidence that nerve damage that is caused by other chemotherapy drugs (not typically used to treat RMS), specifically cisplatin and paclitaxel, may be ameliorated by the use of Vitamin E and glutamine, respectively.

Management of vincristine-associated peripheral neuropathy remains problematic. Although there have been no formal prospective studies, clinical experience indicates that patients over eight years of age tolerate the intensive use of vincristine less well than do younger patients. Two other commonly used chemotherapy drugs, cisplatin and paclitaxel, also cause peripheral neuropathy. Two studies have indicated that the concurrent use of glutamine with cisplatin,41 and Vitamin E with paclitaxel,42 can reduce the incidence and severity of peripheral neuropathy. Although neither agent has been formally evaluated in children with vincristine-associated peripheral neuropathy, anecdotal clinical experience suggests that they are both safe and well-tolerated and may be helpful in some instances.

Irinotecan is a newer drug that was found to be very effective at treating RMS in newly diagnosed patients with metastatic tumors and in patients with recurrent RMS (that is, RMS that relapsed after treatment finished or that never disappeared completely with initial treatment). Uniquely, it is given for ten days every three weeks and although it only infrequently causes severe nausea or vomiting, low blood cell counts, or hair loss, it can produce very severe diarrhea.

Irinotecan (CPT-11) is a promising new drug with very high rates of pre-clinical activity in a murine model of xenografted RMS.13 Clinical trials in children with recurrent disease also demonstrated striking activity.13, 43 The current IRS-V studies are using it in both newly diagnosed children with metastatic tumors (D9802) and in children with recurrent tumors (ARST0121). A pilot clinical trial at MSKCC for patients with intermediate- and high-risk RMS is also using irinotecan as both a "conventional" cytotoxic agent, a potential radiosensitizing agent, and a potential anti-angiogenic agent when given as "maintenance therapy." Although generally well tolerated in terms of the more traditional toxicities such as alopecia, nausea and vomiting, and cytopenias, its use is associated with a high incidence of diarrhea, including severe diarrhea requiring intravenous replenishment. Published guidelines exist for the management of this complication.44

Cyclophosphamide (usually given in combination with vincristine and dactinomycin, or vincristine and doxorubicin) and ifosfamide (usually given in combination with etoposide) can cause damage to the urinary bladder resulting in blood in the urine. Both drugs are given with a "protective" medication, called "mesna" that is effective at reducing the risk of this specific side effect.

Doxorubicin can cause damage to the heart, particularly at higher total (cumulative) doses. Increasingly, in RMS and other types of cancer, it is given with a "protective" medication, called "dexrazoxane", that is effective at reducing the risk of this potentially quite serious complication.

Despite its marked anti-tumor activity, the development of potentially life-threatening cardiac damage, even years after its administration, was one factor leading to the elimination of doxorubicin from recent cooperative group clinical trials for patients with RMS. The use of dexrazoxane has been shown to reduce significantly the risk of cardiac damage associated with doxorubicin therapy45 with no reduction in the anti-tumor effectiveness of the doxorubicin.46

Radiation Therapy

All patients with alveolar RMS – even those whose tumors have been completely removed prior to the start of chemotherapy – and almost all patients with Group II (microscopic residual disease) and Group III (gross residual disease) embryonal RMS – require radiation to maximize their chance for cure. Girls with embryonal RMS of the genital tract (vagina, vulva, cervix, and uterus), for whom initial conservative surgical management is the rule of thumb, can often be managed with serial biopsies, beginning after approximately 12 weeks of chemotherapy treatment, without radiation. Radiation treatments are generally given after 4-5 cycles of chemotherapy have been given (that is, after about 12 weeks), although in selected cases (generally limited to children with parameningeal RMS that has eroded through the base of the skull to extend intracranially) radiation may begin at the same time (or as shortly thereafter as possible) as chemotherapy.

Depending on the site and size and Group of the tumor, between 20 and 28 radiation treatments are given. Ideally, treatment should be planned based on 3-dimensional imaging of the pre-biopsy, pre-chemotherapy tumor. The skill of the Radiation Oncologist in the successful treatment of RMS cannot be overemphasized. Because these are rare tumors, and because most children with RMS are treated on protocols that specify the details of their therapy, the Radiation Oncologist must not only be able to accurately interpret relevant imaging studies to design an appropriate "treatment field" that encompasses all of the original tumor, plus a "margin" of normal surrounding tissue, but to do so at the time specified in the protocol and with an awareness of the "normal tissue tolerance" of surrounding normal structures and the risks of long-term complications of irradiating growing tissue in a young child.

Some of the European cooperative groups that treat children with RMS have tried to reduce or eliminate the use of radiation in very young children or in children whose tumors have disappeared completely after a period of chemotherapy or that were gross totally resected prior to the start of chemotherapy. Unfortunately, although some children can be cured in this fashion, the risk of relapse is significantly greater and it is unclear whether the chance for subsequent cure is as good. Consequently, with the exception of girls with genital tract embryonal RMS, radiation is recommended for all patients with Group III RMS, for all patients with Group II RMS, and for all patients with Group I alveolar RMS. The role of radiation to sites of metastatic disease in children with Stage 4 (or Group IV) RMS is less clear, although children with lung metastases that have disappeared after chemotherapy may have an improved prognosis following low-dose (usually eight treatments) whole-lung irradiation (WLI).

Radiation Therapy

No difference was seen in the IRS-IV study with the use of hyperfractionated versus conventionally fractionated radiation therapy (XRT).36 While most patients with Group III tumors will achieve local control with full-dose XRT, lymph node involvement at diagnosis is correlated with a two-fold increased risk of local treatment failure.47 The same observation has been made for patients with Group II tumors, where the highest risk of local recurrence was seen in patients with microscopic residual disease and regional nodal involvement (Group IIC).48 All patients with alveolar RMS, even those with completely resected tumors, should receive local irradiation.49 European investigators have tried to avoid or limit the use of local irradiation in patients with Groups II50 and Group III51 tumors. Significantly greater local recurrence rates were seen with this approach. The familiarity of the radiation oncologist with treatment guidelines for children with RMS cannot be overstated.52 Use of 3-dimensional imaging and conformal or intensity-modulated radiation therapy (promising new techniques for delivering highly targeted XRT) have produced superior rates of local control particularly for patients with "high-risk" localized tumors such as those with large parameningeal tumors with intracranial extension.53-54 Uniquely among patients with Group II and Group III tumors, girls with unresected genital tract embryonal tumors may not require XRT for local control; optimal management of these patients consists generally of limited initial surgery followed by serial biopsies beginning after a period of approximately twelve weeks of chemotherapy, with definitive surgery or radiation after 24-30 weeks if there is persistent tumor (differentiated rhabdomyoblasts are generally not considered evidence of active tumor in this location).55

Delayed (Second-Look) Surgery

Some children with RMS undergo "delayed" or second-look surgery after their tumor has shrunk following chemotherapy. The reasons for doing this type of operation include trying to eliminate the need for radiation therapy (infrequent) or to allow a "clinically significant" lower dose of radiation to be given post-operatively (common), or to maximize the chance that post-operative radiation will work effectively (particularly for tumors that were very large at the time of diagnosis). Occasionally, a child whose tumor has been treated with radiation will have imaging results that are worrisome and suggest that the tumor has not been killed by the radiation. In these instances, if feasible, surgery may be necessary to remove the residual cancer that has survived the radiation to try to prevent a recurrence at the primary site.

The role of surgery in the management of patients with RMS is clearly site-specific. Superior outcome has been suggested when initial complete, gross total, or even debulking surgery is performed for patients with unfavorable site tumors.56-58 Since a randomized trial of surgical resection is unlikely to ever be accomplished, it will likely never be possible to say whether this improved outcome is a function of surgical resection per se, or whether surgical resectability is merely associated with other factors known to be associated with better outcome such as the presence of gross residual tumor at the time of pre-treatment re-exploration in patients thought to have undergone a "complete" initial resection, smaller tumor size, non-invasive tumors, no nodal involvement, and better response to neoadjuvant chemotherapy. As a general rule, particularly for patients with unfavorable site tumors, maximal function- and cosmetic-sparing surgery is appropriate at the time of diagnosis. For tumors that cannot be resected at the time of diagnosis, second-look surgery should be considered particularly if a complete or gross-total resection is felt to be likely and doing so will permit a significant reduction in the dose of post-operative radiation therapy, or if there is concern about the presence of residual viable tumor after radiation therapy.59 Although "non-mutilating" surgery has been a guiding principle over the past two decades, particularly for patients with bladder/prostate tumors, a recent report has highlighted the important cautionary note that organ retention is not necessarily equated with normal organ function.60

Newer Treatments

Post-relapse survival for the majority of patients with recurrent RMS remains dismal. 95% of recurrences occur within three years of diagnosis. With the exception of a small "favorable risk" group (approximately 20% of relapsing patients) whose 5-year survival approaches 50%, half of patients with recurrent RMS will die of their disease within one year of relapse and 90% of patients will die within five years of relapse.61

Novel therapies are desperately needed for this group of patients.

Targeted Therapies

As better insights are gained into the critical processes of "rhabdomyosarcomagenesis,"62-64 new avenues into biologically-based treatments are being gained. Treatments targeted at interrupting critical growth-factor receptor-ligand interactions, or their downstream targets, appear particularly promising. An autocrine IGF-II pathway plays a role in the growth of RMS;65 disrupting this pathway is one potential biologically "smart" therapy. Growth of RMS xenografts in nude mice can be inhibited using monoclonal antibodies directed against the IGF-I receptor, the receptor that binds IGF-II and mediates its mitogenic signal.66 A newer monoclonal antibody recognizing the human IGF-I receptor was shown to inhibit IGF-I stimulated proliferation in a RMS cell line.67 Highly specific small molecule tyrosine kinase inhibitors targeted against the IGF-I receptor tyrosine kinase have been synthesized and shown to inhibit tumor xenograft growth, both alone and in combination with cytotoxic chemotherapy.68

The recognition that intracellular proteins can be processed and presented as peptides on the cell surface by major histocompatibility complex (MHC) class I molecules has suggested the possibility that tumor-specific mutant gene products may be targets for cytotoxic T cells.69-70 For example, investigators have shown that a peptide derived from a mutant p53 protein is specifically recognized by cytotoxic T cells.71-72 In a similar way, translocation-specific fusion proteins could also potentially be targeted by cytotoxic T cells (CTL). Specifically, the PAX-FKHR fusion protein generated by the t(2;13)(q35;q14) translocation in alveolar RMS is a potential target for CTL therapeutic approaches. Based on pre-clinical murine studies demonstrating that bone-marrow derived Dendritic Cells (DCs) pulsed with Tumor-Associated Antigens (TAA) can generate both Natural Killer (NK) and CD8+ Cytotoxic T-Lymphocytes (CTLs) against RMS,73 pilot clinical studies using PAX-FKHR specific peptide pulsed dendritic cell vaccinations are ongoing. The success of this approach will depend on the ability of tumor cells to present a processed fusion peptide bound to MHC on the cell surface. If this can occur, multiple approaches could then be taken to overcome potential deficits that allowed the tumor to initially escape cellular immunity.74-75

As greater insights are gained into the basic biology of RMS, novel treatment approaches are being developed to try to exploit these "Achilles’ heels" of the tumor cells. Because of the dependency of RMS on IGF-II, promising new drugs have been developed that either block the interaction of the type I IGF receptor with IGF-II, or that block the downstream biological effects that occur after IGF-II binds to its receptor. These agents, though not yet clinically available, offer great promise as both "stand-alone" treatments, or in combination with chemotherapy.

Finally, because of the presence of the unique, tumor-cell specific "translocation" gene in cases of alveolar RMS, the potential exists to utilize immune-based therapies to recognize and kill cells that contain this abnormal gene. Pilot clinical trials are ongoing to evaluate the ability to "vaccinate" patients with alveolar RMS to develop immunity against their own tumors; simultaneously, pilot clinical trials are also ongoing to evaluate the ability of a "genetically matched" sibling’s immune system to control a patient’s alveolar RMS tumor following a "mini"- allogeneic stem cell transplant.

Late Effects of Rhabdomyosarcoma Treatment

The adoption of risk-based therapy for children with RMS is intended to maximize the chance for cure while minimizing the development of short-, intermediate-, and long-term complications. Treatment related late-effects may develop anywhere from months to years after the completion of therapy. Individual chemotherapy agents may have unique toxicities that may not become manifest until many years after the end of therapy, or that may steadily worsen with increased length of follow-up. Damage from radiation therapy, and late complications from surgery, may not become apparent for many years, particularly in growing children. Select well-described complications of treatment include:

  1. Infertility (associated especially with the use of alkylating agents such as cyclophosphamide and ifosfamide): The risk of chemotherapy-induced infertility is much greater for boys than for girls.76 Whenever feasible, even for boys on the cusp of pubertal development, an evaluation should be made of the possibility of sperm cryopreservation.77 Although the subject of intensive laboratory investigation, neither cryopreservation of ovarian tissue nor of ova is currently available as a routinely effective means of fertility preservation for girls;78 fortunately, the risk of infertility appears to be much lower in girls. For girls undergoing pelvic irradiation, or for boys undergoing scrotal irradiation, surgical transposition of the gonad(s) out of the radiation field may be helpful at preserving hormonal function and/or fertility.
  2. Bladder dysfunction: Although "non-mutilating" conservative surgery and full-dose irradiation has become the treatment of choice for bladder preservation in children with bladder/prostate RMS, approximately half of children with "intact" bladders will have one or more symptoms of bladder dysfunction including dribbling, incontinence, and enuresis.60
  3. Radiation damage of head and neck structures: The use of radiation to treat tumors arising in head and neck structures is frequently unavoidable due to the lack of "non-essential" surrounding structures that could be "sacrificed" if complete surgical resection were attempted. Well described complications of radiation include cataract formation after doses to the globe as low as 1000 cGy;79 asymmetric facial growth as a result of permanently arrested bone development and fibrosis ("scarring") of surrounding tissues; chronic sinus infections; growth failure due to pituitary damage;80 and complex and multiple dental abnormalities.81 It is unknown whether more precisely targeted, newer radiation techniques such as Intensity Modulated Radiation Therapy (IMRT), will reduce the risk of late complications from irradiation of head and neck structures.53
  4. Secondary cancer: Perhaps the most devastating late complication of treatment for any type of cancer, not just RMS, is the development of a second form of cancer. The use of chemotherapy and radiation can cause second cancers to develop. Chemotherapy-associated secondary cancers are most commonly leukemias (typically Acute Myeloid Leukemia [AML]), and may be associated with the use of alkylating agents (cyclophosphamide and ifosfamide), and topoisomerase II inhibitors (etoposide and doxorubicin). The risk of secondary leukemia is, fortunately, quite low (generally between 1 and 2%). Radiation is also associated with the development of second cancers, most commonly other sarcomas (either in bone or soft tissue). At the doses of radiation that are currently used to treat children with RMS, the risk of secondary sarcomas is approximately 5% at 20 years.82 Unlike the situation with secondary leukemias, which typically develop within four years of treatment, most cases of secondary sarcomas do not develop until 5+ years after the end of treatment.82 The contribution of underlying "genetic risk factors" to the development of treatment-induced cancers is being actively investigated.

Secondary Cancers

Twenty-two second malignant neoplasms developed among 1770 patients entered onto IRS-I and IRS-II, including 11 radiation-related bone sarcomas and five cases of acute nonlymphoblastic leukemia, at a median of seven years after therapy.83 Three of the affected patients had neurofibromatosis, and the families of seven other of the affected patients had histories compatible with LFS; this suggests that genetic susceptibility plays a significant role in the development of a second malignant neoplasm after treatment for RMS. Early results from IRS-III described the early occurrence of five cases of acute myeloid leukemia in children, as well as one case of osteosarcoma and one case of myelodysplastic syndrome.84 A preliminary reports of SMN in IRS-IV found 14 cases in 13 patients at a median of 3.2 years from diagnosis.85 A more recent update of the IRS experience noted 67 SMN and 2 third malignancies in 4367 patients enrolled on IRS studies from 1972-1997.86 Only seven had a recognized genetic predisposition syndrome. The estimated cumulative incidence for SMN at 20 years was 3.5%. Early concerns about an increased risk of AML/MDS in patients receiving etoposide do not appear to have been substantiated, however, prospective monitoring of the contribution of a strong family history of cancer to the risk of developing a treatment-related SMN is prudent.87

Editor's Note: In closing this article on RMS, we would like to call your attention to the Michael Wolff Memorial Wetland Foundation website. Michael Wolff, 30, passed away on Easter Sunday, April 11, 2004 in M D Anderson Cancer Clinic in Houston, Texas. He had a long ten month battle with alveolar RMS. It all started with just a back ache which was uncommon to this avid duck hunter. This website is to acknowledge this horrible disease and to fulfill Mike's final request of a wetland area, his true passion in life, and to commemorate his wonderful and adventurous life.

Last revision and medical review: 8/2004

By Leonard H. Wexler, MD
Head, Soft Tissue Sarcoma Section
Associate Member
Department of Pediatrics
Memorial Sloan-Kettering Cancer Center
New York, NY

References and Related Articles

1.  Ferrari A, Dileo P, Casanova M, et al.  Rhabdomyosarcoma in adults: A retrospective analysis of 171 patients treated at a single institution.  Cancer 2003; 98:571-580.

2. Hawkins, WG, Hoos A, Antonescu C, et al.  Clinicopathologic analysis of patients with adult rhabdomyosarcoma.  Cancer 2001; 91:794-803.

3.  Little DJ, Ballo MT, Zagars GK, et al.  Adult rhabdomyosarcoma: Outcome following multimodality treatment.  Cancer 2002; 95:377-388.

4.  Esnaola NF, Rubin BP, Baldini EH, et al.  Response to chemotherapy and predictors of survival in adult rhabdomyosarcoma.  Annals of Surgery 2001; 234:215-223.

5.  Furlong MA, Mentzel T, Fanburg-Smith, JC.  Pleiomorphic rhabdomyosarcoma in adults:  A clinicopathologic study of 38 cases with emphasis on morphologic variants and recent skeletal muscle-specific markers.  Modern Pathology 2001; 14:595-603.

6. Li FP, Fraumeni JF Jr.  Soft-tissue sarcoma, breast cancer, and other neoplasms: a familial syndrome.  Annals of Internal Medicine 1969; 71:747-

7. Sung L, Anderson JR, Arndt C, et al.  Neurofibromatosis in children with rhabdomyosarcoma: A report from the Intergroup Rhabdomyosarcoma Study IV.  Journal of Pediatrics 2004; 144:666-668.

8.  Steenman M, Westerveld A, Mannens M.  Genetics of Beckwith-Wiedemann syndrome-associated tumors: common genetic pathways.  Genes Chromosomes and Cancer 2000; 28:1-

9.  Hennekam RC.  Costello syndrome: an overview.  American Journal of Medical Genetics 2003; 117C:42-48.

10. Hartley AL, Birch JM, Blair V, et al. Patterns of cancer in the families of children with soft tissue sarcoma. Cancer 1993; 72:923-

11. Malkin D, Li FP, Strong LC, et al. Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms. Science 1990; 250:1233-.

12. Diller L, Sexsmith E, Gottlieb A, Li FP, Malkin D. Germline p53 mutations are frequently detected in young children with rhabdomyosarcoma. Journal of Clinical Investigation 1995; 95:1606-.

13. Furman WL, Steward CF, Poquette CA, et al.   Direct translation of a protracted irinotecan schedule from a xenograft model to a phase I trial in children.  Journal of Clinical Oncology 1999; 17:1815-

14. Breneman JC, Lyden E, Pappo AS.  Prognostic factors and clinical outcomes in children and adolescents with metastatic rhabdomyosarcoma – A report from the Intergroup Rhabdomyosarcoma Study IV.  Journal of Clinical Oncology  2003; 21:78-84.

15. Neville HL, Andrassy RJ, Lobe TE, et al. Preoperative staging, prognostic factors, and outcome for extremity rhabdomyosarcoma: A preliminary report from the Intergroup Rhabdomyosarcoma Study IV (1991 – 1997).  Journal of Pediatric Surgery 2000; 35:317.

16. Wiener ES, Anderson JR, Ojimba JI et al. Controversies in the management of paratesticular rhabdomyosarcoma: is staging retroperitoneal lymph node dissection necessary for adolescents with resected paratesticular rhabdomyosarcoma? Seminars in Pediatric Surgery 2001;10:146-152.

17. Qualman SJ, Bowen J, Parham DM, Branton PA, Meyer WH. Protocol for the examination of specimens from patients (children and young adults) with rhabdomyosarcoma. Archives of Pathology and Laboratory Medicine 2003;127:1290-1297.

18. Turc-Carel C, Lizard-Nacol S, Justrabo E, et al. Consistent chromosomal translocation in alveolar rhabdomyosarcoma. Cancer Genet Cytogenet 1986;19:361.

19. Douglass EC, Valentine M, Etcubanas E, et al. A specific chromosomal abnormality in rhabdomyosarcoma. Cytogenet Cell Genet 1987;45:148.

20. Shapiro DN, Sublett JE, Li B, et al. Fusion of PAX3 to a member of the forkhead family of transcription factors in human alveolar rhabdomyosarcoma. Cancer Res 1993;53:5108.

21. Davis RJ, DíCruz CM, Lovell MA, Biegel JA, Barr FG. Fusion of PAX7 to FKHR by the variant t(1;13)(p36;q14) translocation in alveolar rhabdomyosarcoma. Cancer Res 1994;54:2869.

22. Khan J, Bittner M, Saal L, et al. cDNA microarrays detect activation of a myogenic transcription program by the PAX3-FKHR fusion oncogene. Proc Natl Acad Sci USA 1999; 96:13264.

23. Ginsberg JP, Davis RJ, Bennicelli JL, Nauta LE, Barr FG. Up-regulation of MET but not neural cell adhesion molecule expression by the PAX3-FKHR fusion protein in alveolar rhabdomyosarcoma. Cancer Res 1998; 58:3542.

24. Gordon AT, Brinkschmidt C, Anderson J, Coleman N, Dockhorn-Dworniczak B, Pritchard-Jones K, Shipley J.  A novel and consistent amplicon at 13q31 associated with alveolar rhabdomyosarcoma.  Genes Chromosomes Cancer 2000; 28:220.

25. Scrable HJ, Witte DP, Lampkin BC, et al. Chromosomal localization of the human rhabdomyosarcoma locus by mitotic recombination mapping. Nature 1987;329:645.

26. Scrable H, Witte D, Shimada H, et al. Molecular differential pathology of rhabdomyosarcoma. Genes Chromosomes Cancer 1989;1:23.

27. Scrable H, Cavenee W, Ghavimi F, et al. A model for embryonal rhabdomyosarcoma tumorigenesis that involves genome imprinting. Proc Natl Acad Sci U S A 1989;86:7480.

28. Rainier S, Johnson LA, Dobry CJ, et al. Relaxation of imprinted genes in human cancer. Nature 1993;362:747.

29. Ogawa O, Eccles MR, Szeto J, et al. Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms’ tumour. Nature 1993;362:749.

30. Feinberg AP. Genomic imprinting and gene activation in cancer. Nat Genet 1993;4:110.

31. Bridge JA, Liu J, Qualman SJ, et al: Genomic gains and losses are similar in genetic and histologic subsets of rhabdomyosarcoma, whereas amplification predominates in embryonal with anaplasia and alveolar subtypes. Genes Chromosomes Cancer 2002; 33:310-321.

32. Bridge JA, Liu J, Weibolt V, et al. Novel genomic imbalances in embryonal rhabdomyosarcoma revealed by comparative genomic hybridization and fluorescence in situ hybridization: an Intergroup Rhabdomyosarcoma Study. Genes Chromosomes Cancer 2000; 27:337.

33. Joshi D, Anderson JR, Paidas C, et al. Age is an independent prognostic factor in rhabdomyosarcoma: a report from the Soft Tissue Sarcoma Committee of the Children's Oncology Group. Pediatric Blood & Cancer. 2004; 42:64-73.

34. Baker KS, Anderson JR, Link MP, et al.  Benefit of intensified therapy for patients with local or regional embryonal rhabdomyosarcoma: Results from the Intergroup Rhabdomyosarcoma Study IV.  Journal of Clinical Oncology 2000; 18:2427-2434.

35. Crist WM, Anderson JR, Meza JL, et al.  Intergroup Rhabdomyosarcoma Study-IV: Results for patients with nonmetastatic disease.  Journal of Clinical Oncology 2001; 19:3091-3102.

36. Donaldson SS, Meza J, Breneman JC, et al.  Results from the IRS-IV randomized trial of hyperfractionated radiotherapy in children with rhabdomyosarcoma – A report from the IRSG.  Internal Journal of Radiation Oncology Biology & Physics  2001; 51:718-728.

37. Sandler E, Lyden E, Ruymann F, et al.  Efficacy of ifosfamide and doxorubicin given as phase II "window" in children with newly diagnosed metastatic rhabdomyosarcoma: A report from the Intergroup Rhabdomyosarcoma Study Group.  Medical and Pediatric Oncology 2001; 37:442-448.  

38. Breitfeld PP, Lyden E, Raney RB, et al.  Ifosfamide and etoposide are superior to vincristine and melphalan for pediatric metastatic rhabdomyosarcoma when administered with irradiation and combination chemotherapy: A report from the Intergroup Rhabdomyosarcoma Study Group.  Journal of Pediatric Hematology/Oncology  2001; 23: 225-233.

39. Weigel BJ, Breitfeld PP, Hawkins D, et al.  Role of high-dose chemotherapy with hematopoietic stem cell rescue in the treatment of metastatic or recurrent rhabdomyosarcoma.  Journal of Pediatric Hematology/Oncology  2001; 23: 272-276.

40. Arndt C, Hawkins D, Anderson JR, et al.  Age is a risk factor for  chemotherapy-induced hepatopathy with vincristine, dactinomycin, and cyclophosphamide.  Journal of Clinical Oncology  2004; 22:1894-1901.

41. Vahdat L, Papadopoulos K, Lange D, et al.  Reduction of paclitaxel-induced peripheral neuropathy with glutamine.  Clinical Cancer Research  2001; 7:1192-1197.

42. Pace A, Savarese A, Picardo M, et al.  Neruoprotective effect of Vitamin E supplementation in patients treated with cisplatin chemotherapy.  Journal of Clinical Oncology  2003; 21:927-931.

43. Cosetti M, Wexler LH, Calleja E, et al.  Irinotecan for pediatric solid tumors: The Memorial Sloan-Kettering experience.  Journal of Pediatric Hematology/Oncology 2002;24:101-105.

44. Benson III, Al B, Ajani JA, Catalano RB, et al.  Recommended guidelines for the treatment of cancer treatment-induced diarrhea.  2004; 22:2918-2926.

45. Wexler LH, Andrich MP, Venzon D, et al.  Randomized trial of the cardioprotective agent ICRF-187 in pediatric sarcoma patients treated with doxorubicin.  Journal of Clinical Oncology 1996  14:362-372.

46. Schwartz CL, Wexler LH, Devidas M, et al.  P9754 therapeutic intensification in non-metastatic osteosarcoma: A COG trial.  Journal of Clinical Oncology 2004; 22(14S):802 (abstract 8514).

47. Wharam MD, Meza J, Anderson J, et al.  Failure pattern and factors predictive of local failure in rhabdomyosarcoma: A report of Group III patients on the Third Intergroup Rhabdomyosarcoma Study.  Journal of Clinical Oncology  2004; 22:1902-1908.

48. Smith LM, Anderson JR, Qualman SJ, et al.  Which patients with microscopic disease and rhabdomyosarcoma experience relapse after therapy? A report from the Soft Tissue Sarcoma Committee of the Children’s Oncology Group.  Journal of Clinical Oncology  2001; 19:4058-4064.

49. Wolden SL, Anderson JR, Crist WM, et al.  Indications for radiotherapy and chemotherapy after complete resection in rhabdomyosarcoma: A report from the Intergroup Rhabdomyosarcoma Studies I to III.  Journal of Clinical Oncology 1999; 17:3468-3475.

50. Schuck A, Mattke AC, Schmidt B, et al.  Group II rhabdomyosarcoma and rhabdomyosarcomalike tumors: Is radiotherapy necessary?  Journal of Clinical Oncology 2004; 22:143-149.

51. Benk V, Rodary C, Donaldson SS, et al.  Parameningeal rhabdomyosarcoma: Results of an international workshop.  International Journal of Radiation Oncology Biology & Physics 1996; 36:533-540.

52. Michalski JM, Meza J, Breneman JC.  Influence of radiation therapy parameters on outcome in children treated with radiation therapy for localized parameningeal rhabdomyosarcoma in Intergroup Rhabdomyosarcoma Study Group trials II through IV.  International Journal of Radiation Oncology Biology & Physics 2004; 59:1027-1038.

53. Wolden SL, La TH, LaQuaglia MP, et al.  Long-term results of three-dimensional conformal radiation therapy for patients with rhabdomyosarcoma.  Cancer 2003; 97:179-185.

54. Wolden SL, Wexler LH, Kraus DH, et al.  Intensity Modulated Radiation Therapy for head and neck rhabdomyosarcoma.  International Journal of Radiation Oncology Biology & Physics 2004, in press.

55. Ardnt CAS, Donaldson SS, Anderson JR, et al.  What constitutes optimal therapy for patients with rhabdomyosarcoma of the female genital tract? Cancer 2001; 91:2454-2468.

56. Hays DM, Lawrence W Jr, Wharam M, et al.  Primary reexcision for patients with "microscopic residual" tumor following initial excision of sarcomas of trunk and extremity sites.  Journal of Pediatric Surgery 1989: 24:5-10.

57. Raney RB, Stoner JA, Walterhouse DO, et al.  Results of treatment of fifty-six patients with localized retroperitoneal and pelvic rhabdomyosarcoma: A report from the Intergroup Rhabdomyosarcoma Study-IV, 1991-1997.  Pediatric Blood and Cancer 2004; 42:1-8.

58. Cecchetto G, Bisogno G, Treuner J, et al.  Role of surgery for nonmetastatic abdominal rhabdomyosarcomas. A report from the Italian and German Soft Tissue Cooperative Group studies.  Cancer 2003; 97:1974-1980.

59. Hays DM, Raney RB, Crist WM, et al.  Secondary surgical procedures to evaluate primary tumor status in patients with chemotherapy-responsive stage III and IV sarcomas: A report from the Intergroup Rhabdomyosarcoma Study  Journal of Pediatric Surgery 1990; 25:1100-1105.

60. Ardnt C, Rodeberg D, Breitfeld PP, et al.  Does bladder preservation (as a surgical principle) lead to retaining bladder function in bladder/prostate rhabdomyosarcoma? Results from Intergroup Rhabdomyosarcoma Study IV.  The Journal of Urology 2004; 171:2396-2403.

61. Pappo AS, Anderson JR, Crist WM.  Survival after relapse in children and adolescents with rhabdomyosarcoma: A report from the Intergroup Rhabdomyosarcoma Study Group.  Journal of Clinical Oncology 1999; 17:3487-3493.

62. Asakura A, Rudnicki MA.  Rhabdomyosarcomagenesis – Novel pathway found.  Cancer Cell 2003; 4:421-422.

63. Fleischmann A, Jochum W, Eferi R, et al.  Rhabdomyosarcoma development in mice lacking Trp53 and Fos: Tumor suppression by the Fos protooncogene.  Cancer Cell 2003; 4:477-482.

64. Sharp R, Recio JA, Jhappan C, et al.  Synergism between INK4a/ARF inactivation and aberrant HGF/SF signaling in rhabdomyosarcomagenesis.  Nature Medicine 2002; 8:1276-1280.

65. El-Badry OM, Minniti C, Kohn EC, et al.  Insulin-like growth factor II acts as an autocrine growth and motility factor in human rhabdomyosarcoma tumors. Cell Growth and Differentiation 1990;1:325.

66. Kalebic T, Tsokos M, Helman LJ. In vivo treatment with antibody against IGF-1 receptor suppresses growth of human rhabdomyosarcoma and down-regulates p34cdc-2. Cancer Research 1994;54:5531.

67. Maloney EK, McLaughlin JL, Dagdigian NE, et al.  An anti-insulin-like growth factor I receptor antibody that is a potent inhibitor of cancer cell proliferation. Cancer Research 2003; 63:5073-5083.

68. Mitsaides CS, Mitsaides NS, McMullan CJ, et al.  Inhibition of the insulin-like growth factor receptor-1 tyrosine kinase activity as a therapeutic strategy for multiple myeloma, other hematologic malignancies, and solid tumors.  Cancer Cell 2004; 5:221-230.

69. Townsend A, Bodmer H. Antigen recognition by class-I restricted T lymphocytes. Annual Review of Immunology 1989; 7:601.

70. Berke G. The CTLS’s kiss of death. Cell 1995; 81:9.

71.Yanuck M, Carbone DP, Pendleton CD, et al. A mutant p53 tumor suppressor protein is a target for peptide-induced CD8+ cytotoxic T-cells. Cancer Researc 1993; 53:3257.

72. Wiedenfeld EA, Fernandez-ViÒa M, Berzofsky JA, Carbone DP. Evidence for selection against human lung cancers bearing p53 missense mutations which occur within the HLA A*0201 peptide consensus motif. Cancer Research 1994; 54:1175.

73. van den Broeke LT, Daschbach Em, Thomas EK, et al. Dendritic cell-induced activation of adaptive and innate antitumor immunity.  The Journal of Immunology  2003; 171:5842-5852..  Also see the clinical trial, "Pilot Study of Autologous T-Cell Transplantation with Vaccine Driven Expansion of Anti-Tumor Effectors After Cytoreductive Therapy in Metastatic Pediatric Sarcomas", by clicking here.

74. Guinan EC, Gribben JG, Boussiotis VA, Freeman GJ, Nadler LM. Pivotal role of the B7:CD28 pathway in transplantation tolerance and tumor immunity. Blood 1994; 84:3261.

75. Schmidt W, Schweighoffer T, Herbst E, et al. Cancer vaccines: the interleukin 2 dosage effect. Proceedings of the National Academy of Sciences of the United States of America (PNA) 1995; 92:4711.

76. Lentz RD, Bergstein J, Steffes MW, et al. Postpubertal evaluation of gonadal function following cyclophosphamide therapy before and during puberty.  Journal of Pediatrics 1977; 91:385.

77. Bahadur, G, Ling KLE, Hart R, et al.  Semen quality and cryopreservation in adolescent cancer patients.  Human Reproduction 2002; 12:3157-3161

78. Oktay K, Nugent D, Newton H, Salha O, Chatterjee P, Gosden RG. Isolation and characterization of primordial follicles from fresh and cryopreserved human ovarian tissue. Fertility and Sterility 1997; 67:481-486.

79. Raney RB, Anderson JR, Kollath J, et al.  Late effects of therapy in 94 patients with localized rhabdomyosarcoma of the orbit: Report from the Intergroup Rhabdomyosarcoma Study (IRS)-III, 1984-1991.  Medical and Pediatric Oncology 2000;34:413.

80. Raney RB, Asmar L, Vassilopoulou-Sellin R, et al. Late complications of therapy in 213 children with localized, nonorbital soft-tissue sarcoma of the head and neck: A descriptive report from the Intergroup Rhabdomyosarcoma Studies (IRS)-II and –III. Medical and Pediatric Oncology 1999; 33:362.

81. Estilo CL, Huryn JM, Kraus DH et al. Effects of therapy on dentofacial development in long-term survivors of head and neck rhabdomyosarcoma: the Memorial Sloan-Kettering Cancer Center experience. Journal of Pediatric Hematology/Oncology 2003; 25:215-222.

82. Kuttesch JF Jr, Wexler LH, Marcus RB, et al.  Second malignancies after Ewing’s sarcoma: radiation dose-dependency of secondary sarcomas.  Journal of Clinical Oncology 1996; 14:2818-2825.

83. Heyn R, Haeberlen V, Newton WA, et al. Second malignant neoplasms in children treated for rhabdomyosarcoma. J Clin Oncol 1993;11:262.

84. Heyn R, Khan F, Ensign LG, et al. Acute myeloid leukemia in patients treated for rhabdomyosarcoma with cyclophosphamide and low-dose etoposide on Intergroup Rhabdomyosarcoma Study III: an interim report. Med Pediatr Oncol 1994;23:99.

85. Pappo A, Anderson J, Qualman S, Donaldson S, Crist W.  Second malignant neoplasms in IRSG-IV: A preliminary report from the Intergroup Rhabdomyosarcoma Study Group.  (abstract) Proc Am Soc Clin Oncol 2000;19:584.

86. Spunt SL, Meza JL, Anderson JR et al. Second Malignant Neoplasms (SMN) in Children Treated for Rhabdomyosarcoma: a Report from the Intergroup Rhabdomyosarcoma Studies (IRS) I-IV [abstract]. Proc Annu Meet Am Soc Clin Oncol. 2001;20:2173.

87. Smith MA, Rubinstein L, Ungerleider RS. Therapy-related acute myeloid leukemia following treatment with epipodophyllotoxins: establishing the risks. Med Pediatr Oncol 1994;23:86.


Stories and Support

Will you share your story?

We would like to fill this page with survival stories that offer hope and encouragement to everyone learning about rhabdomyosarcoma. Please consider sharing your story.

Grant writes about finding support

I’m surviving sarcoma first and foremost because of fellow sarcoma survivors. When diagnosed with rhabdomyosarcoma in the head and lungs at age 26, a dear friend mine, a survivor of osteosarcoma, guided me through the beginning steps of treatment. Suggesting what doctors to see and what measures to take, my friend gave me the initial tools to fight my battle, including a few tricks to enduring the hell of chemotherapy. Websites like the Sarcoma Initiative and list-serves like ACOR’s Rhabdo list gave me the medical resources and information to further educate myself on the best options available.

Sarcoma, because it is so rare, can be an extremely isolating disease, so finding others in similar battles was very important to me. Their courage added to mine. Their successes gave me hope. They wanted me to learn from their mistakes and their triumphs. I joined a virtual army with a very real enemy. We know we can’t win every battle, but we plan to eventually win the war.

Recently, I met a scared young man who had just been diagnosed with rhabdomyosarcoma. I took off my blue sarcoma bracelet, handed it to him, and was able to proudly say, "You are not alone."

Len introduces us to Andrew

I would like to introduce you do my hero, my son Andrew. He was diagnosed with orbital rhabdomyosarcoma when he was 9 years old. His initial protocol was for nine months of chemotherapy and five weeks of radiation. He unfortunately relapsed shortly after completing his treatments, and after more chemotherapy and surgeries, his medical team decided to perform a very radical surgery, which had only been performed once in the history of SickKids, and that was the removal of his entire orbit.

Andrew never once complained or cried or asked "why me?" Even while going through all his treatments and surgeries, including the loss of his left eye, he continued to play rep hockey as a goalie. He led his team to the city championship the following year and he had the best goals against in the entire league. He has continued to persevere and inspire many; he excels at most sports including basketball and golf.

In 2003, Andrew was named an Ontario Junior Citizen of the year, and in 2004, Today’s Parent Magazine named him as one of the top five individuals in Canada that are making a difference in the lives of Canadian children. He has a cancer research fund at SickKids which, to date, has raised $350,000 for this worthy cause.

Today Andrew is 18 years old, and a straight "A" student in college. He is also pursuing his real estate license, which he plans on having before his 19th birthday. He is a gifted song writer and performer who is currently in studio recording an album. He coaches minor basketball and continues to inspire many, including his dad. Most important, he is cancer free!

John shares a moment in his journey

I remember the moment when I realized that we had entered the cancer realm, which no one enters voluntarily. The doctors had ruled out our initial suspicion that my son had an inflamed appendix. Instead they had confirmed that he had a stage 3 or 4 rhabdomyosarcoma. We were told that a course of radiation and chemotherapy would be prescribed, and that this treatment would in all likelihood have a negative impact on my son’s reproductive fertility. It was recommended that he "bank" a sperm specimen in the event that his treatment rendered him sterile. We were referred to a sperm bank near our house.

At the appointed time we pulled into the neighborhood where the facility was located, parked our car, and located the office on the upper floor of a two story building. While my son was filling out forms I walked to the window overlooking the street below. Across the street was a luxury hotel. A professional basketball team from the NBA was staying at the hotel and a line of about a dozen boys, close to my son’s age, had formed on the sidewalk outside the hotel’s entrance. These boys were waiting to intercept some of the players and plead for them to autograph their basketballs.

I suddenly had the feeling that I was looking at a world that we previously inhabited, but no longer do inhabit. I was looking at that world from a new one that we had suddenly and reluctantly been inducted into. The window separated these very different worlds, and we would probably never again be part of that other world.

Sarah writes about bonding with other parents

A woman was sitting in the surgical waiting room while my son was having an MRI. We thought the plastic surgeon had made a mistake and nicked an artery in the last cleft surgery. I cried and this woman reached out and said, "My daughter is here having back surgery. She has cancer." "Poor woman," I thought, "at least my son is not that bad."

Ten minutes later, we were exchanging numbers, bonding. My son was that bad. Rhabdomyosarcoma — a word we could not pronounce. One we had never heard before. A word for a 7 cm tumor that could kill my son. This woman became my rock, my best friend, my world on my ward.

I could tell you about the 11 month rollercoaster journey through chemo and radiation. I could tell you about the children throwing up, screaming, and begging the pokes to stop. It all has been said before. That crushing feeling when your world is stopped completely. A life that was secure suddenly seems hopeless. The feeling of not knowing if your baby will live or die. This woman’s daughter did pass away, and my son was saved, now cancer free.

Instead, I will tell you about the moment you realize that you have become part of a world you can never fully leave, where you bond with parents on the ward despite race or status. You fall in love with strangers; you share great scans, devastation, elation and death. A friend dies and your son lives and even though both are extremes at opposite ends of the spectrum, neither parent will ever leave the cancer world nor return to normal. You end up fighting until all the little faces become recognized, until there is hope, and through hope you save the fate of one more child.

The Online Rhadomyosarcoma Support Group at ACOR

This group provides a network of friends who are dealing with issues related to rhabdomyosarcoma. An ACOR "Mailing List" is a free, non-moderated discussion mechanism for patients, caregivers, researchers, and medical professionals to exchange messages with each other. Messages are "posted" by someone on the list (i.e., a member of the support group) and cover a wide range of topics, e.g., patient experiences, research articles, clinical trials, current treatment practices and alternative treatments. A posting often results in an "online discussion" of the topic. Sometimes, one or more medical professionals are members of a support group and may comment on a posting.

Focus on Rhabdo

The website of a community-anchored, multi-disciplinary consortium of “Rhabdo Activists.”

Connect on Facebook

The following Facebook groups provide opportunities to exchange messages with others who are dealing with rhabdomyosarcoma.

Find Treatment and Support

We maintain listings of sarcoma treatment centers, local support groups and organizations that provide financial assistance to sarcoma patients and their loved-ones.

Rhabdomyosarcoma Cancer Research

The Liddy Shriver Sarcoma Initiative has funded more than $190,000 in rhabdomyosarcoma research grants. Rhabdomyosarcoma often strikes very young children, older children and adolescents, and treatment can involve aggressive chemotherapy, radiation therapy and surgery. It is our hope that research will lead to newer and better treatments for those who are diagnosed with rhabdomyosarcoma.

The following research studies were funded by the Initiative after sarcoma experts agreed that they were clinically relevant and scientifically sound:

Modeling Treatment Response of NF1-Deleted Sarcoma

Modeling Treatment Response of NF1-Deleted Sarcoma$69,000 Grant: In this study, investigators from Duke University will use their mouse model of NF1-deleted sarcomas to explore the role of NF1 mutations in the development and therapeutic response of rhabdomyosarcoma, undifferentiated pleomorphic sarcoma, and malignant peripheral nerve sheath tumor.

This grant was co-funded by the Liddy Shriver Sarcoma Initiative in April 2013. It was made possible by a generous gift from the Thumbs Up For Lane Goodwin Childhood Cancer Foundation and by donations made in honor of Brett Reed, Craig Dion, Denise Grove, Michael Cretella, and Samara Sheller.

Immunotherapy for Pediatric Sarcomas

Immunotherapy for Pediatric Sarcomas$50,000 Grant: In this study, investigators from the National Cancer Institute will alter T cells so that they recognize and kill osteosarcoma and rhabdomyosarcoma cells as if they were virus-infected cells. They will then use blocking antibodies to prevent the cancer from dampening the T cells' immune reaction. The investigators hope that the research will improve current immunotherapies and make them more effective in treating sarcomas.

This grant was funded by the Liddy Shriver Sarcoma Initiative in December 2012.

The Hippo Pathway in Alveolar Rhabdomyosarcoma

The Role of Cytoplasmic p27 in Metastatic Osteosarcoma$50,000 Grant: In this study, investigators at Duke University Medical Center are working to provide a platform for designing new mouse models and therapeutic approaches for Alveolar Rhabdomyosarcoma. The researchers hope that they might ultimately find new therapeutic strategies for rhabdomyosarcoma and additional childhood sarcomas.

This grant was awarded by the Liddy Shriver Sarcoma Initiative in August 2012. It was made possible by generous gifts from the Jordan Paganelli Sarcoma Foundation and from the families and friends of Timothy "Tim" Yeates, Anna Rogotzke, Dillon Wolford, Ashley Miller, Harper Creek and Teri Marriage-Kuespert.

Study of Tissue Samples

$25,000 Grant: This tissue study was performed in conjunction with a clinical trial on several types of sarcoma, including Rhabdomyosarcoma.

Elizabeth Shriver Memorial Research Award

$25,000 Grant: In June 2004, Dr. Frederic Barr of the University of Pennsylvania was the recipient of a $25,000 Elizabeth Shriver Memorial Research Award. He is well known for his work on gene fusions in rhabdomyosarcoma (RMS), so he is well familiar with the complex genes in this tumor. Most of the alveolar type of RMS, a childhood tumor, form when two genes are abnormally stuck together (PAX and FKHR genes). For unknown reasons, some alveolar RMS lack this finding and yet still form and grow. In this grant, Dr. Barr tried to determine how and why some rhabdomyosarcomas do not have the usual gene fusion, which causes abnormal growth. Dr. Barr published an ESUN article based on his work.

  • Figure 1: Age at Diagnosis for children with RMS.
    Approximately two-thirds of children with RMS are less than ten years of age at the time of diagnosis. RMS is most common in children 1-4 years of age and uncommon in infants less than one year of age.
  • Figure 2: Case 1: A 7-year old boy with orbital RMS.
    MRI of the orbit shows a soft tissue mass arising in the supero-medial aspect of the left orbit displacing the globe outward and laterally.
  • Figure 3: Case 2 A 14-year old girl with parameningeal RMS.
    MRI of the sinuses shows a large, invasive soft tissue mass centered in the sinonasal region invading into both the right and left orbits and extending intra-cranially through the base of the skull.
  • Figure 4: Case 3: An 18-year old man with prostate RMS.
    MRI of the prostate showing a large soft tissue mass on the right side of the pelvis compressing the posterior wall of the urinary bladder and the anterior wall of the rectum.
  • Figure 5
  • Figure 6: Microscopic appearance of Embryonal RMS.
    Embryonal RMS cells are typically less dense and more spindly. Evidence of skeletal muscle lineage may or may not be evident upon routine microscopic examination. Confirmatory immunostaining with antibodies directed against desmin, vimentin, actin, and myogenin support the diagnosis of RMS.
  • Figure 7: Microscopic appearance of Alveolar RMS.
    Alveolar RMS cells are typically smaller and rounder and more densely cellular. Architecturally, they may have the appearance of "lining-up" along pseudo-spaces that are reminiscent of the small air sacs in the lung (alveoli).
  • Figure 8
    Figure 8: Over-expression of Insulin-Like Growth Factor Type II (IGF-II) through Loss-of-Heterozygosity at 11p15.
  • Figure 9
    Figure 9: Reciprocal translocation between PAX and FKHR creates a hybrid "oncogene."