Cargando…

Retrospective Analysis of Bevacizumab in Combination with Fotemustine in Chinese Patients with Recurrent Glioblastoma Multiforme

The aim of this study was to assess the activity and safety of bevacizumab (BEV) and fotemustine (FTM) for the treatment of recurrent glioblastoma multiforme (GBM) patients and explore the potential prognostic parameters on survival. This study retrospectively analyzed all patients with GBM who were...

Descripción completa

Detalles Bibliográficos
Autores principales: Liu, Zhiguang, Zhang, Guanqun, Zhu, Liang, Wang, Jiangbo, Liu, Dongbo, Lian, Lifei, Liu, Jianlin, Lai, Tianbao, Zhuang, Xiaorong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4348597/
https://www.ncbi.nlm.nih.gov/pubmed/25789324
http://dx.doi.org/10.1155/2015/723612
_version_ 1782359949984137216
author Liu, Zhiguang
Zhang, Guanqun
Zhu, Liang
Wang, Jiangbo
Liu, Dongbo
Lian, Lifei
Liu, Jianlin
Lai, Tianbao
Zhuang, Xiaorong
author_facet Liu, Zhiguang
Zhang, Guanqun
Zhu, Liang
Wang, Jiangbo
Liu, Dongbo
Lian, Lifei
Liu, Jianlin
Lai, Tianbao
Zhuang, Xiaorong
author_sort Liu, Zhiguang
collection PubMed
description The aim of this study was to assess the activity and safety of bevacizumab (BEV) and fotemustine (FTM) for the treatment of recurrent glioblastoma multiforme (GBM) patients and explore the potential prognostic parameters on survival. This study retrospectively analyzed all patients with GBM who were treated with at least one cycle of BEV and FTM from July 2010 to October 2012. A total of 176 patients with recurrent GBM were enrolled. The response rate and disease control rate were 46.6% and 90.9%, respectively. A 6-month PFS rate of 33.3% (95% CI: 26.5%–40.3%) and a median PFS of 5.0 (95% CI: 2.4–7.5) months were observed. The median OS was 8.0 (95% CI: 6.7–9.2) months. Multivariate analysis showed that risk factors with a significant influence on the PFS of all patients were Karnofsky Performance Status (KPS) (≥70 versus <70, HR = 0.53, 95% CI: 0.39–0.73, and P = 0.01) and MGMT status (methylated versus unmethylated, HR = 0.69, 95% CI: 0.52–0.97, and P = 0.04). The most common treatment-related adverse events were fatigue, proteinuria, hypophonia, hypertension, thrombocytopenia, anemia, and neutropenia. In conclusion, combination of BEV with FTM is well tolerated and may derive some clinical benefits in recurrent GBM patients. Higher KPS and MGMT promoter hypermethylation were suggested to be associated with prolonged survival.
format Online
Article
Text
id pubmed-4348597
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Hindawi Publishing Corporation
record_format MEDLINE/PubMed
spelling pubmed-43485972015-03-18 Retrospective Analysis of Bevacizumab in Combination with Fotemustine in Chinese Patients with Recurrent Glioblastoma Multiforme Liu, Zhiguang Zhang, Guanqun Zhu, Liang Wang, Jiangbo Liu, Dongbo Lian, Lifei Liu, Jianlin Lai, Tianbao Zhuang, Xiaorong Biomed Res Int Research Article The aim of this study was to assess the activity and safety of bevacizumab (BEV) and fotemustine (FTM) for the treatment of recurrent glioblastoma multiforme (GBM) patients and explore the potential prognostic parameters on survival. This study retrospectively analyzed all patients with GBM who were treated with at least one cycle of BEV and FTM from July 2010 to October 2012. A total of 176 patients with recurrent GBM were enrolled. The response rate and disease control rate were 46.6% and 90.9%, respectively. A 6-month PFS rate of 33.3% (95% CI: 26.5%–40.3%) and a median PFS of 5.0 (95% CI: 2.4–7.5) months were observed. The median OS was 8.0 (95% CI: 6.7–9.2) months. Multivariate analysis showed that risk factors with a significant influence on the PFS of all patients were Karnofsky Performance Status (KPS) (≥70 versus <70, HR = 0.53, 95% CI: 0.39–0.73, and P = 0.01) and MGMT status (methylated versus unmethylated, HR = 0.69, 95% CI: 0.52–0.97, and P = 0.04). The most common treatment-related adverse events were fatigue, proteinuria, hypophonia, hypertension, thrombocytopenia, anemia, and neutropenia. In conclusion, combination of BEV with FTM is well tolerated and may derive some clinical benefits in recurrent GBM patients. Higher KPS and MGMT promoter hypermethylation were suggested to be associated with prolonged survival. Hindawi Publishing Corporation 2015 2015-02-18 /pmc/articles/PMC4348597/ /pubmed/25789324 http://dx.doi.org/10.1155/2015/723612 Text en Copyright © 2015 Zhiguang Liu et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Liu, Zhiguang
Zhang, Guanqun
Zhu, Liang
Wang, Jiangbo
Liu, Dongbo
Lian, Lifei
Liu, Jianlin
Lai, Tianbao
Zhuang, Xiaorong
Retrospective Analysis of Bevacizumab in Combination with Fotemustine in Chinese Patients with Recurrent Glioblastoma Multiforme
title Retrospective Analysis of Bevacizumab in Combination with Fotemustine in Chinese Patients with Recurrent Glioblastoma Multiforme
title_full Retrospective Analysis of Bevacizumab in Combination with Fotemustine in Chinese Patients with Recurrent Glioblastoma Multiforme
title_fullStr Retrospective Analysis of Bevacizumab in Combination with Fotemustine in Chinese Patients with Recurrent Glioblastoma Multiforme
title_full_unstemmed Retrospective Analysis of Bevacizumab in Combination with Fotemustine in Chinese Patients with Recurrent Glioblastoma Multiforme
title_short Retrospective Analysis of Bevacizumab in Combination with Fotemustine in Chinese Patients with Recurrent Glioblastoma Multiforme
title_sort retrospective analysis of bevacizumab in combination with fotemustine in chinese patients with recurrent glioblastoma multiforme
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4348597/
https://www.ncbi.nlm.nih.gov/pubmed/25789324
http://dx.doi.org/10.1155/2015/723612
work_keys_str_mv AT liuzhiguang retrospectiveanalysisofbevacizumabincombinationwithfotemustineinchinesepatientswithrecurrentglioblastomamultiforme
AT zhangguanqun retrospectiveanalysisofbevacizumabincombinationwithfotemustineinchinesepatientswithrecurrentglioblastomamultiforme
AT zhuliang retrospectiveanalysisofbevacizumabincombinationwithfotemustineinchinesepatientswithrecurrentglioblastomamultiforme
AT wangjiangbo retrospectiveanalysisofbevacizumabincombinationwithfotemustineinchinesepatientswithrecurrentglioblastomamultiforme
AT liudongbo retrospectiveanalysisofbevacizumabincombinationwithfotemustineinchinesepatientswithrecurrentglioblastomamultiforme
AT lianlifei retrospectiveanalysisofbevacizumabincombinationwithfotemustineinchinesepatientswithrecurrentglioblastomamultiforme
AT liujianlin retrospectiveanalysisofbevacizumabincombinationwithfotemustineinchinesepatientswithrecurrentglioblastomamultiforme
AT laitianbao retrospectiveanalysisofbevacizumabincombinationwithfotemustineinchinesepatientswithrecurrentglioblastomamultiforme
AT zhuangxiaorong retrospectiveanalysisofbevacizumabincombinationwithfotemustineinchinesepatientswithrecurrentglioblastomamultiforme