A phase II study of temozolemide vs. procarbazine in patients with glioblastoma multiforme at first relapse

  • W. K.A. Yung
  • , R. E. Albright
  • , J. Olson
  • , R. Fredericks
  • , K. Fink
  • , M. D. Prados
  • , M. Brada
  • , A. Spence
  • , R. J. Hohl
  • , W. Shapiro
  • , M. Glantz
  • , H. Greenberg
  • , R. G. Selker
  • , N. A. Vick
  • , R. Rampling
  • , H. Friedman
  • , P. Phillips
  • , J. Bruner
  • , N. Yue
  • , D. Osoba
  • S. Zaknoen, V. A. Levin

Research output: Contribution to journalArticlepeer-review

889 Scopus citations

Abstract

A randomized, multicentre, open-label, phase II study compared temozolomide (TMZ), an oral second-generation alkylating agent, and procarbazine (PCB) in 225 patients with glioblastoma multiforme at first relapse. Primary objectives were to determine progression-free survival (PFS) at 6 months and safety for TMZ and PCB in adult patients who failed conventional treatment. Secondary objectives were to assess overall survival and health-related quality of life (HRQL). TMZ was given orally at 200 mg/m2/day or 160 mg/m2/day (prior chemotherapy) for 5 days, repeated every 28 days. PCB was given orally at 150 mg/m2/day or 125 mg/m2/day (prior chemotherapy) for 28 days, repeated every 56 days. HRQL was assessed using the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30 [+3]) and the Brain Cancer Module 20 (BCM20). The 6-month PFS rate for patients who received TMZ was 21%, which met the protocol objective. The 6-month PFS rate for those who received PCB was 8% (P = 0.008, for the comparison). Overall PFS significantly improved with TMZ, with a median PFS of 12.4 weeks in the TMZ group and 8.32 weeks in the PCB group (P = 0.0063). The 8-month overall survival rate for TMZ patients was 60% vs. 44% for PCB patients (P = 0.019). Freedom from disease progression was associated with maintenance of HRQL, regardless of treatment received. TMZ had an acceptable safety profile; most adverse events were mild or moderate in severity. (C) 2000 Cancer Research Campaign.

Original languageEnglish (US)
Pages (from-to)588-593
Number of pages6
JournalBritish Journal of Cancer
Volume83
Issue number5
DOIs
StatePublished - 2000

All Science Journal Classification (ASJC) codes

  • Oncology
  • Cancer Research

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