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...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , |
---|---|
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 |