Cargando…

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

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 sa...

Descripción completa

Detalles Bibliográficos
Autores principales: Yung, W K A, Albright, R E, Olson, J, Fredericks, R, Fink, K, Prados, M D, Brada, M, Spence, A, Hohl, R J, Shapiro, W, Glantz, M, Greenberg, H, Selker, R G, Vick, N A, Rampling, R, Friedman, H, Phillips, P, Bruner, J, Yue, N, Osoba, D, Zaknoen, S, Levin, V A
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2000
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363506/
https://www.ncbi.nlm.nih.gov/pubmed/10944597
http://dx.doi.org/10.1054/bjoc.2000.1316
_version_ 1782153721837256704
author Yung, W K A
Albright, R E
Olson, J
Fredericks, R
Fink, K
Prados, M D
Brada, M
Spence, A
Hohl, R J
Shapiro, W
Glantz, M
Greenberg, H
Selker, R G
Vick, N A
Rampling, R
Friedman, H
Phillips, P
Bruner, J
Yue, N
Osoba, D
Zaknoen, S
Levin, V A
author_facet Yung, W K A
Albright, R E
Olson, J
Fredericks, R
Fink, K
Prados, M D
Brada, M
Spence, A
Hohl, R J
Shapiro, W
Glantz, M
Greenberg, H
Selker, R G
Vick, N A
Rampling, R
Friedman, H
Phillips, P
Bruner, J
Yue, N
Osoba, D
Zaknoen, S
Levin, V A
author_sort Yung, W K A
collection PubMed
description 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/m(2)/day or 150 mg/m(2)/day (prior chemotherapy) for 5 days, repeated every 28 days. PCB was given orally at 150 mg/m(2)/day or 125 mg/m(2)/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 6-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. © 2000 Cancer Research Campaign
format Text
id pubmed-2363506
institution National Center for Biotechnology Information
language English
publishDate 2000
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-23635062009-09-10 A phase II study of temozolomide vs. procarbazine in patients with glioblastoma multiforme at first relapse Yung, W K A Albright, R E Olson, J Fredericks, R Fink, K Prados, M D Brada, M Spence, A Hohl, R J Shapiro, W Glantz, M Greenberg, H Selker, R G Vick, N A Rampling, R Friedman, H Phillips, P Bruner, J Yue, N Osoba, D Zaknoen, S Levin, V A Br J Cancer Regular Article 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/m(2)/day or 150 mg/m(2)/day (prior chemotherapy) for 5 days, repeated every 28 days. PCB was given orally at 150 mg/m(2)/day or 125 mg/m(2)/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 6-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. © 2000 Cancer Research Campaign Nature Publishing Group 2000-09 2000-08-16 /pmc/articles/PMC2363506/ /pubmed/10944597 http://dx.doi.org/10.1054/bjoc.2000.1316 Text en Copyright © 2000 Cancer Research Campaign https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Regular Article
Yung, W K A
Albright, R E
Olson, J
Fredericks, R
Fink, K
Prados, M D
Brada, M
Spence, A
Hohl, R J
Shapiro, W
Glantz, M
Greenberg, H
Selker, R G
Vick, N A
Rampling, R
Friedman, H
Phillips, P
Bruner, J
Yue, N
Osoba, D
Zaknoen, S
Levin, V A
A phase II study of temozolomide vs. procarbazine in patients with glioblastoma multiforme at first relapse
title A phase II study of temozolomide vs. procarbazine in patients with glioblastoma multiforme at first relapse
title_full A phase II study of temozolomide vs. procarbazine in patients with glioblastoma multiforme at first relapse
title_fullStr A phase II study of temozolomide vs. procarbazine in patients with glioblastoma multiforme at first relapse
title_full_unstemmed A phase II study of temozolomide vs. procarbazine in patients with glioblastoma multiforme at first relapse
title_short A phase II study of temozolomide vs. procarbazine in patients with glioblastoma multiforme at first relapse
title_sort phase ii study of temozolomide vs. procarbazine in patients with glioblastoma multiforme at first relapse
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363506/
https://www.ncbi.nlm.nih.gov/pubmed/10944597
http://dx.doi.org/10.1054/bjoc.2000.1316
work_keys_str_mv AT yungwka aphaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT albrightre aphaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT olsonj aphaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT fredericksr aphaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT finkk aphaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT pradosmd aphaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT bradam aphaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT spencea aphaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT hohlrj aphaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT shapirow aphaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT glantzm aphaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT greenbergh aphaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT selkerrg aphaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT vickna aphaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT ramplingr aphaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT friedmanh aphaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT phillipsp aphaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT brunerj aphaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT yuen aphaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT osobad aphaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT zaknoens aphaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT levinva aphaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT yungwka phaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT albrightre phaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT olsonj phaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT fredericksr phaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT finkk phaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT pradosmd phaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT bradam phaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT spencea phaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT hohlrj phaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT shapirow phaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT glantzm phaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT greenbergh phaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT selkerrg phaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT vickna phaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT ramplingr phaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT friedmanh phaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT phillipsp phaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT brunerj phaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT yuen phaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT osobad phaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT zaknoens phaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse
AT levinva phaseiistudyoftemozolomidevsprocarbazineinpatientswithglioblastomamultiformeatfirstrelapse