Response and progression in recurrent malignant glioma

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Hess, K. R.
Wong, E. T.
Jaeckle, K. A.
Kyritsis, A. P.
Levin, V. A.
Prados, M. D.
Yung, W. K.

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peer-reviewed

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Neuro Oncol

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In this article we report the results of a study of the relationship between response and progression in 375 patients with recurrent glioma enrolled in phase II chemotherapy trials. We reviewed the records of patients from 8 consecutive phase II trials, including 225 patients with recurrent glioblastoma multiforme and 150 with recurrent anaplastic astrocytoma. Median age was 45 years (range, 15-82) and median Karnofsky performance score was 80 (range, 60-100). Forty-one patients (11%) had more than two prior resections and/or more than two prior chemotherapy regimens. Best response was complete (n = 1) or partial (n = 33) in 34 patients (9%). Median time to response was 14 weeks, and median response duration was 44 weeks. Simon-Makuch estimates for 52-week progression-free survival for patients progression-free at 13 weeks were 48% for response and 28% for nonresponse. When response was treated as a time-dependent covariate in a Cox proportional hazards regression analysis, response was associated with significantly lower failure rates (hazard ratio 0.5; 95% confidence interval 0.3-0.8; P = 0.0016). This study showed that response in recurrent glioma is associated with a significant reduction in progression rates.

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Actuarial Analysis, Adolescent, Adult, Aged, Aged, 80 and over, Antineoplastic Combined Chemotherapy Protocols/*therapeutic use, Astrocytoma/drug therapy/mortality/radiotherapy, Brain Neoplasms/*drug therapy/mortality/radiotherapy, Carboplatin/administration & dosage, Combined Modality Therapy, Disease Progression, Disease-Free Survival, Eflornithine/administration & dosage, Female, Fluorouracil/administration & dosage, Glioblastoma/drug therapy/mortality/radiotherapy, Glioma/*drug therapy/mortality/radiotherapy, Humans, Interferon-beta/administration & dosage, Male, Menogaril/administration & dosage, Middle Aged, Neoplasm Recurrence, Local/*drug therapy/mortality, Procarbazine/administration & dosage, Prognosis, Proportional Hazards Models, Texas/epidemiology, Treatment Outcome, Tretinoin/administration & dosage

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http://www.ncbi.nlm.nih.gov/pubmed/11550320

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en

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Πανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικής

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