Skip to main content
Clinical Trials/NCT00003375
NCT00003375
Completed
Phase 2

A Phase II Study of Observation in Favorable Low-Grade Glioma and a Phase II Study of Radiation With or Without PCV Chemotherapy in Unfavorable Low-Grade Glioma

Radiation Therapy Oncology Group0 sites370 target enrollmentOctober 1998

Overview

Phase
Phase 2
Intervention
radiation therapy
Conditions
Brain and Central Nervous System Tumors
Sponsor
Radiation Therapy Oncology Group
Enrollment
370
Primary Endpoint
Overall Survival
Status
Completed
Last Updated
last year

Overview

Brief 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. It is not yet known whether radiation therapy combined with chemotherapy is more effective than radiation therapy alone in treating patients with low-grade glioma.

PURPOSE: Phase II/III trial to evaluate observation and to compare the effectiveness of radiation therapy with or without combination chemotherapy in treating patients with low-grade glioma.

Detailed Description

OBJECTIVES: * Identify the overall survival of low-risk adult patients with supratentorial low-grade glioma who are observed postoperatively. * Compare the overall survival of high-risk adult patients with supratentorial low-grade glioma who receive postoperative external beam radiotherapy with or without procarbazine, lomustine, and vincristine (PCV) chemotherapy. * Compare the toxic effects of postoperative radiotherapy with or without PCV chemotherapy in patients with unfavorable low-grade glioma. OUTLINE: This is a randomized study. Patients are stratified according to tumor subtype (astrocytoma \[mixed-astro dominant or equal astro/oligo mix\] vs oligodendroglioma \[mixed-oligo dominant\]), age (younger than 40 vs at least 40), Karnofsky performance status (60-80% vs 90-100%), and contrast enhancement on preoperative scan (present vs absent). Patients with low-risk disease (younger than 40 years old whose tumors have been surgically removed) are assigned to arm I. Patients with high-risk disease (at least 40 years old or who have had incomplete tumor removal) are randomized to arm II or III. * Arm I (low-risk patients): Patients are observed. Patients may receive treatment if tumor recurs. * Arm II (high-risk patients): Patients receive daily external beam radiotherapy 5 days a week for 6 weeks. * Arm III (high-risk patients): Patients receive radiotherapy as in arm II followed by chemotherapy 1 month later. Chemotherapy consists of oral lomustine on day 1, vincristine IV on days 8 and 29, and oral procarbazine on days 8-21. Each course of chemotherapy lasts 8 weeks. Patients may receive up to 6 courses of chemotherapy. Patients are followed every 4 months for 1 year, every 6 months for 2 years, and then annually thereafter. PROJECTED ACCRUAL: Approximately 252 patients will be accrued within 5.25 years.

Registry
clinicaltrials.gov
Start Date
October 1998
End Date
May 14, 2018
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Arms & Interventions

Radiation therapy

Radiation therapy only.

Intervention: radiation therapy

Radiation plus PCV chemotherapy

Radiation and Procarbazine/CCNU/Vincristine (PCV) chemotherapy

Intervention: lomustine

Radiation plus PCV chemotherapy

Radiation and Procarbazine/CCNU/Vincristine (PCV) chemotherapy

Intervention: procarbazine hydrochloride

Radiation plus PCV chemotherapy

Radiation and Procarbazine/CCNU/Vincristine (PCV) chemotherapy

Intervention: vincristine sulfate

Radiation plus PCV chemotherapy

Radiation and Procarbazine/CCNU/Vincristine (PCV) chemotherapy

Intervention: radiation therapy

Outcomes

Primary Outcomes

Overall Survival

Time Frame: From randomization to date of death or last follow-up. Analysis occurs after all patients have been potentially followed for 5 years or 80 deaths have been reported.

Secondary Outcomes

  • Progression-free Survival(From randomization to the date of progression, death or last follow-up. Analysis ours at the same time as the primary outcome analysis.)
  • The severe or worse toxicities (>= grade 3) of unfavorable patients(From start of treatment to end of follow-up)

Similar Trials