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Effectiveness of lomustine and bevacizumab in progressive glioblastoma: a meta-analysis
BACKGROUND: Glioblastomas (GBMs) are the most aggressive type of glial brain tumors. Despite aggressive treatment with surgery and chemoradiation, GBMs invariably relapse and tumors are progressive. Controversy remains on optimal treatment of patients with recurrent GBMs. Data from previous trials h...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6005326/ https://www.ncbi.nlm.nih.gov/pubmed/29942135 http://dx.doi.org/10.2147/OTT.S160685 |
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author | Song, Jie Xue, Yue-Qin Zhao, Ming-Ming Xu, Peng |
author_facet | Song, Jie Xue, Yue-Qin Zhao, Ming-Ming Xu, Peng |
author_sort | Song, Jie |
collection | PubMed |
description | BACKGROUND: Glioblastomas (GBMs) are the most aggressive type of glial brain tumors. Despite aggressive treatment with surgery and chemoradiation, GBMs invariably relapse and tumors are progressive. Controversy remains on optimal treatment of patients with recurrent GBMs. Data from previous trials have suggested that the addition of bevacizumab (BEV) to lomustine (CCNU) might improve overall survival (OS) as compared with that with monotherapies. The aim of this study was to compare the efficacy of BEV in addition to CCNU versus single-agent therapy in patients with recurrent GBM. METHODS: Electronic databases were searched for eligible literature updated in December 2017. Trials assessing the effectiveness of CCNU and BEV in progressive GBM were included, of which the main outcomes were progression-free survival (PFS) and OS. All the data were pooled with the corresponding 95% confidence intervals (CIs) using RevMan software. Sensitivity and heterogeneity were quantitatively evaluated. RESULTS: Three randomized clinical trials were identified, including 574 patients (combination group: 358, monotherapies group: 216). The combination group treated with BEV and CCNU showed improvement in PFS (OR = 0.49; 95% CI, 0.41–0.59; p < 0.00001). No significant differences were, however, found in patients in terms of the OS (OR = 0.84; 95% CI, 0.68–1.03; p = 0.09). CONCLUSION: Although treatment with CCNU plus BEV prolonged PFS, it did not confer OS advantage over monotherapies in patients with progressive GBM. The encouraging results of the addition of CCNU to BEV warrant investigation in further randomized trials. |
format | Online Article Text |
id | pubmed-6005326 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-60053262018-06-25 Effectiveness of lomustine and bevacizumab in progressive glioblastoma: a meta-analysis Song, Jie Xue, Yue-Qin Zhao, Ming-Ming Xu, Peng Onco Targets Ther Original Research BACKGROUND: Glioblastomas (GBMs) are the most aggressive type of glial brain tumors. Despite aggressive treatment with surgery and chemoradiation, GBMs invariably relapse and tumors are progressive. Controversy remains on optimal treatment of patients with recurrent GBMs. Data from previous trials have suggested that the addition of bevacizumab (BEV) to lomustine (CCNU) might improve overall survival (OS) as compared with that with monotherapies. The aim of this study was to compare the efficacy of BEV in addition to CCNU versus single-agent therapy in patients with recurrent GBM. METHODS: Electronic databases were searched for eligible literature updated in December 2017. Trials assessing the effectiveness of CCNU and BEV in progressive GBM were included, of which the main outcomes were progression-free survival (PFS) and OS. All the data were pooled with the corresponding 95% confidence intervals (CIs) using RevMan software. Sensitivity and heterogeneity were quantitatively evaluated. RESULTS: Three randomized clinical trials were identified, including 574 patients (combination group: 358, monotherapies group: 216). The combination group treated with BEV and CCNU showed improvement in PFS (OR = 0.49; 95% CI, 0.41–0.59; p < 0.00001). No significant differences were, however, found in patients in terms of the OS (OR = 0.84; 95% CI, 0.68–1.03; p = 0.09). CONCLUSION: Although treatment with CCNU plus BEV prolonged PFS, it did not confer OS advantage over monotherapies in patients with progressive GBM. The encouraging results of the addition of CCNU to BEV warrant investigation in further randomized trials. Dove Medical Press 2018-06-13 /pmc/articles/PMC6005326/ /pubmed/29942135 http://dx.doi.org/10.2147/OTT.S160685 Text en © 2018 Song et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Song, Jie Xue, Yue-Qin Zhao, Ming-Ming Xu, Peng Effectiveness of lomustine and bevacizumab in progressive glioblastoma: a meta-analysis |
title | Effectiveness of lomustine and bevacizumab in progressive glioblastoma: a meta-analysis |
title_full | Effectiveness of lomustine and bevacizumab in progressive glioblastoma: a meta-analysis |
title_fullStr | Effectiveness of lomustine and bevacizumab in progressive glioblastoma: a meta-analysis |
title_full_unstemmed | Effectiveness of lomustine and bevacizumab in progressive glioblastoma: a meta-analysis |
title_short | Effectiveness of lomustine and bevacizumab in progressive glioblastoma: a meta-analysis |
title_sort | effectiveness of lomustine and bevacizumab in progressive glioblastoma: a meta-analysis |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6005326/ https://www.ncbi.nlm.nih.gov/pubmed/29942135 http://dx.doi.org/10.2147/OTT.S160685 |
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