Phase II diaziquone-based chemotherapy trials in patients with anaplastic supratentorial astrocytic neoplasms.
- 1 March 1987
- journal article
- research article
- Published by American Society of Clinical Oncology (ASCO) in Journal of Clinical Oncology
- Vol. 5 (3) , 464-471
- https://doi.org/10.1200/jco.1987.5.3.464
Abstract
We treated 103 patients with histologically confirmed anaplastic supratentorial astrocytic neoplasms with either diaziquone (AZQ) and carmustine (BCNU) or AZQ and procarbazine. There were 74 patients with glioblastoma multiforme (GBM) and 29 patients with anaplastic astrocytoma (AA). AZQ plus BCNU produced partial (PR) or unequivocal responses in seven of 32 (21.9%) patients with GBMs and three of ten (30%) patients with AAs. Two patients with GBMs (6.3%) and five patients with AAs (50%) showed stable disease (SD). AZQ plus procarbazine produced PRs or unequivocal responses in five of 42 (11.9%) patients with GBMs and nine of 19 (47.4%) patients with AAs. Eight patients with GBMs (19%) and one patient with an AA (5.2%) showed SD. In addition to histologic diagnosis, only the Karnofsky performance-status (KPS) rating independently influenced response and survival. Differences in response rates between the two regimens were not significant, although estimated median survival after adjusting for performance status was slightly better with AZQ plus BCNU than with AZQ plus procarbazine (P = .031). Neither age nor prior chemotherapy were significant independent risk factors. Toxicity was mild and primarily hematologic. We conclude that these AZQ-based regimens have activity in patients with recurrent anaplastic gliomas, but that they are not clearly superior to other agents in current use. The histologic diagnosis of GBM is associated with a significantly worse prognosis than AA, and we believe that this important distinction must be recognized in phase II as well as phase III trials.This publication has 13 references indexed in Scilit:
- Etoposide (VP-16-213) in malignant brain tumors: a phase II study.Journal of Clinical Oncology, 1984
- Treatment of patients with recurrent primary brain tumors with AZQNeurology, 1984
- TREATMENT OF HUMAN GLIOMA AND MEDULLOBLASTOMA TUMOR LINES IN ATHYMIC MICE WITH DIAZIQUONE AND DIAZIQUONE-BASED DRUG-COMBINATIONS1984
- Comparison of postoperative radiotherapy and combined postoperative radiotherapy and chemotherapy in the multidisciplinary management of malignant gliomas. A joint radiation therapy oncology group and eastern cooperative oncology group studyCancer, 1983
- Evaluation of prognostic factors in chemotherapy of recurrent brain tumors.Journal of Clinical Oncology, 1983
- TREATMENT OF 5 SUBCUTANEOUS HUMAN GLIOMA TUMOR LINES IN ATHYMIC MICE WITH CARMUSTINE, PROCARBAZINE, AND MITHRAMYCIN1983
- COMPARISONS OF CARMUSTINE, PROCARBAZINE, AND HIGH-DOSE METHYLPREDNISOLONE AS ADDITIONS TO SURGERY AND RADIOTHERAPY FOR THE TREATMENT OF MALIGNANT GLIOMA1983
- Phase II Studies of Dianhydrogalactitol-Based Combination Chemotherapy for Recurrent Brain TumorsOncology, 1981
- Prediction of BCNU Pulmonary Toxicity in Patients with Malignant GliomasNew England Journal of Medicine, 1980
- Evaluation of BCNU and/or radiotherapy in the treatment of anaplastic gliomasJournal of Neurosurgery, 1978