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Combination Chemotherapy and Radiation Therapy in Treating Patients With Newly Diagnosed Rhabdomyosarcoma

Conditions

Rhabdomyosarcoma

Trial Phase

Phase 3

Trial Purpose and Description

Trial Purpose

This randomized phase III trial is studying two different combination chemotherapy regimens to compare how well they work when given together with radiation therapy in treating patients with newly diagnosed rhabdomyosarcoma. Drugs used in chemotherapy, such as vincristine sulfate, dactinomycin, cyclophosphamide, and irinotecan hydrochloride, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Radiation therapy uses high-energy x-rays to kill tumor cells. Giving combination chemotherapy together with radiation therapy may kill more tumor cells. It is not yet known which combination chemotherapy regimen is more effective when given together with radiation therapy in treating patients with rhabdomyosarcoma.


Trial Description


PRIMARY OBJECTIVES:

I. To compare the early response rates, failure-free survival (FFS), and survival of
patients with intermediate-risk rhabdomyosarcoma (RMS) treated with surgery, radiotherapy,
and vincristine (vincristine sulfate), dactinomycin and cyclophosphamide (VAC) or VAC
alternating with vincristine, irinotecan (irinotecan hydrochloride) (VI).

SECONDARY OBJECTIVES:

I. To compare FFS, local control, and survival of patients with intermediate-risk RMS
treated with VAC and early (week 4) radiotherapy vs delayed (week 10) radiotherapy, using
data from Intergroup Rhabdomyosarcoma Study (IRS)-IV for historic comparison.

II. To compare the acute and late effects of VAC to VAC alternating with VI, including the
toxicity associated with concurrent VI and radiotherapy.

III. To compare the acute and late effects of VAC as delivered on this study to D9803 VAC.

IV. To correlate change in fludeoxyglucose F-18 positron emission tomography (FDG-PET)
maximum standard uptake value (SUVmax) from week 1 to week 4 and 15 with FFS.

V. For VI treated patients, to correlate patient UDP glucuronosyltransferase 1 family,
polypeptide A1 (UGT1A1) genotype with VI toxicity. VI. To correlate cytochrome P450, family
2, subfamily B, polypeptide 6 (CYP2B6), cytochrome P450, family 2, subfamily C, polypeptide
9 (CYP2C9), and glutathione S-transferase alpha 1 (GSTA1) genotypes with VAC toxicity.

VII. To prospectively evaluate and validate gene expression values with the intent to define
the best diagnostic predictors and more powerful prognostic classifiers.

VIII. To assess the frequency of bladder dysfunction in patients with bladder, prostate, and
pelvic sites of RMS 3-6 years after study enrollment.

OUTLINE: Patients are randomized to 1 of 2 treatment arms within 42 days of initial surgery
or biopsy.

ARM I (VAC): Patients receive VAC chemotherapy comprising vincristine sulfate IV over 1
minute on day 1 of weeks 1-13, 16, 19-25, 28, 31-37, and 40; dactinomycin IV over 1-5
minutes on day 1 of weeks 1, 4, 13, 16, 19, 22, 25, 28, 31, 34, 37, and 40; and
cyclophosphamide IV over 1 hour on day 1 of weeks 1, 4, 7, 10, 13, 16, 19, 22, 25, 28, 31,
34, 37, and 40.

ARM II (VAC/VI): Patients receive VAC chemotherapy alternating with VI chemotherapy
comprising vincristine sulfate IV over 1 minute on day 1 of weeks 1-13,16, 17, 19, 20,
22-26, 28, 31-34, 37, 38, and 40; dactinomycin IV over 1-5 minutes on day 1 of weeks 1,13,
22, 28, 34, and 40; cyclophosphamide IV over 1 hour on day 1 of weeks 1,10, 13, 22, 28, 34,
and 40; and irinotecan hydrochloride IV over 90 minutes on days 1-5 of weeks 4, 7, 16, 19,
25, 31, and 37.

In both arms, treatment continues in the absence of disease progression or unacceptable
toxicity. Patients* in both arms also undergo radiotherapy 5 days a week for 4-6 weeks
beginning in week 4 (except patients with alveolar RMS rendered group I by amputation OR
patients needing week 1 emergency radiotherapy for symptomatic spinal cord compression).

NOTE: *Individualized local control plan that deviates from protocol-mandated radiotherapy
allowed for patients =< 24 months of age.

After completion of study treatment, patients are followed up every 2-4 months for 4 years
and then annually for 5-10 years.

Participation Guidelines

Age:
Up to 49 Years
Gender:
Both

Eligibility Criteria


Inclusion Criteria:

- Patients with newly diagnosed embryonal RMS, botryoid or spindle cell variants of
embryonal RMS, ectomesenchymoma, or alveolar RMS are eligible for this study

- Enrollment on COG-D9902 to confirm local histologic diagnosis with central pathology
review is required for all patients

- Patients may be enrolled on ARST0531 and start protocol treatment prior to receipt of
central pathology review results

- Patient must have Intermediate-risk RMS defined as:

- Embryonal, botryoid, or spindle cell RMS, or ectomesenchymoma: stage 2 or 3 and
group III OR

- Alveolar RMS: stage 1-3 and group I-III

- Staging ipsilateral retroperitoneal lymph node dissection (SIRLND) is required for
all patients >= 10 years of age with paratesticular tumors and for patients < 10
years with clinically or radiographically involved lymph nodes (except when extensive
lymph node involvement, defined as two or more lymph nodes > 2 cm in dimension, is
identified by imaging studies)

- Regional lymph node sampling or sentinel lymph node procedure is required for
histologic evaluation in patients with extremity tumors

- Clinically or radiographically enlarged nodes should be sampled for histologic
evaluation

- Detection of metastasis by optional FDG PET (not required for study enrollment); FDG
PET may detect abnormalities suggestive of metastasis not identified by bone scan,
computed tomography (CT), or bone marrow aspiration/biopsy; the prognostic
significance of FDG PET-detected abnormalities is not clear; FDG PET-detected
abnormalities MUST be confirmed to be metastases by an additional imaging modality
(such as magnetic resonance imaging [MRI] or CT) OR pathologic confirmation; unless
FDG PET abnormalities are confirmed by another imaging modality or biopsy, FDG PET
abnormalities will NOT be considered evidence of metastasis

- Patients must have a performance status of 0, 1, or 2; the Lansky performance score
should be used for patients < 16 years and the Karnofsky performance score for
patients >= 16 years

- Patients who have received prior chemotherapy (excluding steroids) or radiation
therapy, except for patients transferring from ARST0331 (low-risk study), are not
eligible

- Creatinine clearance or radioisotope glomerular filtration rate (GFR) >= 70
ml/min/1.73 m^2 or a serum creatinine based on age/gender as follows:

- 1 month to < 6 months: 0.4 mg/dL

- 6 months to < 1 year: 0.5 mg/dL

- 1 to < 2 years: 0.6 mg/dL

- 2 to < 6 years: 0.8 mgt/dL

- 6 to < 10 years: 1 mg/dL

- 10 to < 13 years: 1.2 mg/dL

- 13 to < 16 years: 1.5 mg/dL (males) or 1.4 mg/dL (females)

- >= 16 years: 1.7 mg/dL (males) or 1.4 mg/dL (females)

- Patients with urinary tract obstruction by tumor must meet the renal function
criteria AND must have unimpeded urinary flow established via decompression of the
obstructed portion of the urinary tract

- Total bilirubin =< 1.5 x upper limit of normal for age

- Peripheral absolute neutrophil count (ANC) >= 750/uL

- Platelet count >= 75,000/uL (transfusion independent)

- No evidence of uncontrolled infection

- Patients must be able to undergo radiation therapy, if necessary, as specified in the
protocol

- Female patients of childbearing potential must have a negative pregnancy test

- Female patients who are breast feeding must agree to stop breast feeding

- Sexually active patients of childbearing potential must be willing to use effective
contraception during therapy and for at least 1 month after treatment is completed

- All patients and/or their parents or legal guardians must sign a written informed
consent

- All institutional, Food and Drug Administration (FDA), and National Cancer Institute
(NCI) requirements for human studies must be met
Sponsor:
Children's Oncology Group
National Cancer Institute (NCI)
Dates:
December 2006
Last Updated:
February 26, 2014
Study HIC#:
1008007246

Clinicaltrials.gov ID: NCT00354835