Radiation Therapy Plus Combination Chemotherapy in Treating Children With Medulloblastoma

Last updated: July 31, 2014
Sponsor: Children's Oncology Group
Overall Status: Completed

Phase

3

Condition

Brain Tumor

Brain Cancer

Gliomas

Treatment

N/A

Clinical Study ID

NCT00002875
A9961
CDR0000065160
CCG-A9961
POG-A9961
  • Ages 3-22
  • All Genders

Study Summary

RATIONALE: Radiation therapy uses high energy x-rays to damage tumor cells. Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining radiation therapy with chemotherapy may kill more tumor cells. It is not yet known which chemotherapy regimen is more effective when combined with radiation therapy for treating medulloblastoma.

PURPOSE: Randomized phase III trial to compare two combination chemotherapy treatments plus radiation therapy in treating children with newly diagnosed medulloblastoma.

Eligibility Criteria

Inclusion

DISEASE CHARACTERISTICS: Pathologically confirmed posterior fossa medulloblastoma (CCG diagnosis code 2041) Localized disease required, i.e.: No more than 1.5 square centimeters of residual tumor on postoperative contrast-enhanced CT or MRI (preferably within 72 hours but no more than 14 days after surgery) No evidence of metastatic disease on pre- and postoperative MRI of spine (with dye enhancement) and lumbar cerebrospinal fluid (CSF) cytology within 3 days prior to surgery Cytologic analysis of ventricular CSF allowed only if medical contraindication to lumbar puncture and with approval of study chairperson Brain stem involvement eligible

PATIENT CHARACTERISTICS: Age: 3 to 21 at diagnosis Performance status: Not specified Hematopoietic: ANC greater than 1,500/mm3 Platelet count greater than 100,000/mm3 Hemoglobin greater than 10 g/dL Hepatic: Bilirubin less than 1.5 mg/dL ALT less than 1.5 times normal Renal: Nuclear glomerular filtration rate or creatinine clearance greater than 70 mL/min per 1.73 square meters

PRIOR CONCURRENT THERAPY: No prior radiotherapy or chemotherapy (other than corticosteroids) No more than 31 days since definitive surgery

Study Design

Total Participants: 421
Study Start date:
December 01, 1996
Estimated Completion Date:
January 31, 2011

Study Description

OBJECTIVES: I. Assess whether a cyclophosphamide-containing combination chemotherapy regimen increases progression-free survival compared to a lomustine-containing regimen in children with newly diagnosed, average-risk medulloblastoma. II. Determine progression-free and overall survival of children treated with craniospinal radiotherapy and local boost radiotherapy for a total dose of 5580 cGy followed by adjuvant lomustine/cisplatin/vincristine vs. cyclophosphamide/cisplatin/vincristine. III. Determine the long-term neurocognitive, endocrinologic, and cardiopulmonary sequelae associated with craniospinal radiotherapy, local boost radiotherapy, and adjuvant chemotherapy in these children, and determine whether replacement of lomustine with cyclophosphamide alters the incidence and degree of sequelae. IV. Determine whether cellular and biologic parameters, including tumor molecular genetic analysis, DNA ploidy, mitotic activity markers, and immunohistochemical analysis, are correlated with progression-free survival, overall survival, and patterns of disease relapse in these patients. V. Evaluate the utility of routine magnetic resonance imaging surveillance studies of the head and spine in detecting subclinical recurrent disease.

OUTLINE: This is a randomized study. Patients are stratified by participating institution. Following surgery, patients are randomized to one of two groups. The first group receives craniospinal irradiation followed by a boost to the primary tumor. Beginning within 1 week after initiation of radiotherapy, patients receive vincristine weekly for 8 doses. Beginning 6 weeks after the completion of radiotherapy, patients receive adjuvant lomustine/vincristine/cisplatin every 6 weeks for a total of 8 courses. The second group receives craniospinal irradiation plus vincristine as above, followed by adjuvant cyclophosphamide/vincristine/cisplatin every 6 weeks for a total of 8 courses. Patients are followed every 3 months for 1 year, every 6 months for 2 years, then annually.

PROJECTED ACCRUAL: It is anticipated that 240-300 patients will be entered over 4 years.

Connect with a study center

  • Princess Margaret Hospital for Children

    Perth, Western Australia 6001
    Australia

    Site Not Available

  • British Columbia Children's Hospital

    Vancouver, British Columbia V6H 3V4
    Canada

    Site Not Available

  • IWK Grace Health Centre

    Halifax, Nova Scotia B3J 3G9
    Canada

    Site Not Available

  • University of Puerto Rico School of Medicine Medical Sciences Campus

    San Juan, 00936-5067
    Puerto Rico

    Site Not Available

  • Clinique de Pediatrie

    Geneva, 1211
    Switzerland

    Site Not Available

  • Long Beach Memorial Medical Center

    Long Beach, California 90806
    United States

    Site Not Available

  • Children's Hospital Los Angeles

    Los Angeles, California 90027-0700
    United States

    Site Not Available

  • Jonsson Comprehensive Cancer Center, UCLA

    Los Angeles, California 90095-1781
    United States

    Site Not Available

  • Children's Hospital of Orange County

    Orange, California 92668
    United States

    Site Not Available

  • UCSF Cancer Center and Cancer Research Institute

    San Francisco, California 94115-0128
    United States

    Site Not Available

  • Children's Hospital of Denver

    Denver, Colorado 80218
    United States

    Site Not Available

  • Children's National Medical Center

    Washington, District of Columbia 20010-2970
    United States

    Site Not Available

  • University of Chicago Cancer Research Center

    Chicago, Illinois 60637
    United States

    Site Not Available

  • Indiana University Cancer Center

    Indianapolis, Indiana 46202-5265
    United States

    Site Not Available

  • University of Iowa Hospitals and Clinics

    Iowa City, Iowa 52242
    United States

    Site Not Available

  • Via Christi Regional Medical Center

    Wichita, Kansas 67214
    United States

    Site Not Available

  • MBCCOP - LSU Medical Center

    New Orleans, Louisiana 70112
    United States

    Site Not Available

  • University of Michigan Comprehensive Cancer Center

    Ann Arbor, Michigan 48109-0752
    United States

    Site Not Available

  • University of Minnesota Cancer Center

    Minneapolis, Minnesota 55455
    United States

    Site Not Available

  • Mayo Clinic Cancer Center

    Rochester, Minnesota 55905
    United States

    Site Not Available

  • Children's Mercy Hospital

    Kansas City, Missouri 64108
    United States

    Site Not Available

  • University of Nebraska Medical Center

    Omaha, Nebraska 68198-3330
    United States

    Site Not Available

  • St. Joseph's Hospital and Medical Center

    Paterson, New Jersey 07503
    United States

    Site Not Available

  • Herbert Irving Comprehensive Cancer Center

    New York, New York 10032
    United States

    Site Not Available

  • Memorial Sloan-Kettering Cancer Center

    New York, New York 10021
    United States

    Site Not Available

  • NYU School of Medicine's Kaplan Comprehensive Cancer Center

    New York, New York 10016
    United States

    Site Not Available

  • Lineberger Comprehensive Cancer Center, UNC

    Chapel Hill, North Carolina 27599-7295
    United States

    Site Not Available

  • Children's Hospital Medical Center - Cincinnati

    Cincinnati, Ohio 45229-3039
    United States

    Site Not Available

  • Ireland Cancer Center

    Cleveland, Ohio 44106-5065
    United States

    Site Not Available

  • Children's Hospital of Columbus

    Columbus, Ohio 43205-2696
    United States

    Site Not Available

  • Doernbecher Children's Hospital

    Portland, Oregon 97201-3098
    United States

    Site Not Available

  • Children's Hospital of Philadelphia

    Philadelphia, Pennsylvania 19104
    United States

    Site Not Available

  • Children's Hospital of Pittsburgh

    Pittsburgh, Pennsylvania 15213
    United States

    Site Not Available

  • Saint Jude Children's Research Hospital

    Memphis, Tennessee 38105-2794
    United States

    Site Not Available

  • Vanderbilt Cancer Center

    Nashville, Tennessee 37232-6838
    United States

    Site Not Available

  • University of Texas - MD Anderson Cancer Center

    Houston, Texas 77030
    United States

    Site Not Available

  • Huntsman Cancer Institute

    Salt Lake City, Utah 84132
    United States

    Site Not Available

  • Cancer Center, University of Virginia HSC

    Charlottesville, Virginia 22908
    United States

    Site Not Available

  • Children's Hospital and Regional Medical Center - Seattle

    Seattle, Washington 98105
    United States

    Site Not Available

  • Fred Hutchinson Cancer Research Center

    Seattle, Washington 98109
    United States

    Site Not Available

  • University of Wisconsin Comprehensive Cancer Center

    Madison, Wisconsin 53792
    United States

    Site Not Available

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