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.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
318
200 mg/m2 body surface on days 1-5 every 28 days for 8 cycles; and again for another 4 cycles at primary progression
54-60 Gy in 28-30 fractions over 6-7 weeks
University of Heidelberg
Heidelberg, Baden-Wurttemberg, Germany
Neurology and Radiotherapy
Tübingen, Baden-Wurttemberg, Germany
Klinikum Aschaffenburg
Aschaffenburg, Germany
Nervenklinik
Bamberg, Germany
Charite
Berlin, Germany
Neurosurgery
Düsseldorf, Germany
Radiotherapy
Erlangen, Germany
Neurology
Essen, Germany
Neurosurgery
Frankfurt, Germany
Neurosurgery
Kiel, Germany
...and 2 more locations
Time-to-treatment-failure defined as progression after radiotherapy and one chemotherapy in either sequence
Time frame: 1999-2008
Progression-free survival Overall Survival Toxicity Response rates
Time frame: 1999-2012
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