Randomized Phase III Study of Sequential Radiochemotherapy of Anaplastic Glioma With PCV or Temozolomide

Last updated: July 16, 2008
Sponsor: Neuro-Oncology Working Group of the German Cancer Society
Overall Status: Completed

Phase

3

Condition

Astrocytoma

Oligodendroglioma

Glioblastoma Multiforme

Treatment

N/A

Clinical Study ID

NCT00717210
NOA-04
  • Ages > 18
  • All Genders

Study Summary

Background: The optimal treatment of anaplastic gliomas is controversial. Standard of care in most centers is still radiotherapy. This phase III study compared the efficacy and safety of radiotherapy vs chemotherapy in patients (pts) with newly-diagnosed, supratentorial gliomas of WHO grade III.

Methods: Pts were randomized 2:1:1 between June 1999 and February 2005 in 34 German centers to receive (i) a 6-week course of radiotherapy (1,8-2 Gy fractions, total dose 54-60 Gy) or (ii) four 6-week cycles of CCNU at 110 mg mg/m2 on day 1, vincristine at 2 mg on days 8 and 29 and procarbazine at 60 mg/m2 on days 8-21 or eight 4-week cycles of 200 mg/m2 temozolomide on days 1-5. Treatment was stopped prematurely at disease progression or occurrence of unacceptable toxicity. At this time or at disease progression, treatment in the radiotherapy group was continued with one of the chemotherapies (1:1 randomization) and with radiotherapy in both chemotherapy groups. The primary endpoint was time-to-treatment-failure (TTF) defined as progression after radiotherapy and one chemotherapy in either sequence, or any time before if further therapy could not be employed. Assuming a 50% improvement in TTF of starting with chemotherapy, 318 pts were to be enrolled to provide 80% power to achieve statistical significance at a one-sided level of 0.05.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • written informed consent

  • centrally confirmed anaplastic glioma according to the WHO-classification 1998/2000

  • age ≥ 18 years

  • Karnofsky performance status (KPS) of 70 or higher

  • no prior systemic chemotherapy or radiation therapy of the brain

  • no HIV infection

  • adequate bone marrow reserve, liver function, and renal function

  • Patients on corticosteroids had to be on a stable or decreasing dosage within the 14days prior to randomization

Exclusion

Exclusion Criteria:

  • Glioblastoma

  • infratentorial localization of the tumor

  • pregnancy or lactation period

  • serious medical or neurological comorbidity

  • additional malignancy requiring radio- or chemotherapy

  • known hypersensitivity against study drugs

  • inability to swallow

  • frequent emesis

  • psychological. familial, sociological or geographical situations impairing compliancewith F/U examinations

  • parallel participation in other studies

Study Design

Total Participants: 318
Study Start date:
June 01, 1999
Estimated Completion Date:
March 31, 2008

Connect with a study center

  • Neurology and Radiotherapy

    Tübingen, Baden-Württemberg 72076
    Germany

    Site Not Available

  • University of Heidelberg

    Heidelberg, Baden-Württemberg 69120
    Germany

    Site Not Available

  • Neurology and Radiotherapy

    Tübingen, Baden-Württemberg 72076
    Germany

    Site Not Available

  • Klinikum Aschaffenburg

    Aschaffenburg,
    Germany

    Site Not Available

  • Nervenklinik

    Bamberg,
    Germany

    Site Not Available

  • Charite

    Berlin,
    Germany

    Site Not Available

  • Neurosurgery

    Düsseldorf,
    Germany

    Site Not Available

  • Neurosurgery

    Düsseldorf,
    Germany

    Site Not Available

  • Radiotherapy

    Erlangen,
    Germany

    Site Not Available

  • Neurology

    Essen,
    Germany

    Site Not Available

  • Neurosurgery

    Frankfurt,
    Germany

    Site Not Available

  • Neurosurgery

    Kiel,
    Germany

    Site Not Available

  • Neurosurgery

    Mainz,
    Germany

    Site Not Available

  • County District Hospital

    Regensburg,
    Germany

    Site Not Available

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