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Efficacy and safety of long-term therapy for high-grade glioma with temozolomide: A meta-analysis

Further treatments are warranted in preventing recurrence or progression for high-grade glioma (HGG) patients having achieved stable disease with tolerable toxicity after the Stupp regimen (6 cycles of temozolomide). This meta-analysis aims to extensively evaluate the safety, feasibility, and effica...

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Autores principales: Xu, Weilin, Li, Tao, Gao, Liansheng, Zheng, Jingwei, Shao, Anwen, Zhang, Jianmin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5584285/
https://www.ncbi.nlm.nih.gov/pubmed/28881684
http://dx.doi.org/10.18632/oncotarget.17401
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author Xu, Weilin
Li, Tao
Gao, Liansheng
Zheng, Jingwei
Shao, Anwen
Zhang, Jianmin
author_facet Xu, Weilin
Li, Tao
Gao, Liansheng
Zheng, Jingwei
Shao, Anwen
Zhang, Jianmin
author_sort Xu, Weilin
collection PubMed
description Further treatments are warranted in preventing recurrence or progression for high-grade glioma (HGG) patients having achieved stable disease with tolerable toxicity after the Stupp regimen (6 cycles of temozolomide). This meta-analysis aims to extensively evaluate the safety, feasibility, and efficacy of long-term therapy with temozolomide (>6 cycles) for these patients. We systematically searched the pubmed, Embase and Chinese Biomedical (CBM) databases using the strategy of combination of free-text words and MeSH terms. The efficacy indicators are hazard ratio (HR) for the pooled analysis of overall survival (OS) and progression free survival (PFS). The safety indicator is risk ratio (RR) for the pooled analysis of adverse effects. Six studies comprising a total number of 396 patients met all inclusion and exclusion criteria were included. No heterogeneity and publication bias were observed across each study. It was found that patients could obtain benefits from long-term administration of temozolomide both in OS (HR 2.39, 95% CI 1.82–3.14) and PFS (HR 2.12, 95% CI 1.56–2.89). In addition, the results showed that the patients receiving long-term administration of temozolomide did not experience additional toxicity over that of the Stupp regimen (6 cycles of temozolomide). It could be concluded that it's efficacious and safe for HGG patients to receive long-term therapy with temozolomide. Nevertheless, more randomized controlled trials (RCTs) should be carried out to verify this conclusion.
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spelling pubmed-55842852017-09-06 Efficacy and safety of long-term therapy for high-grade glioma with temozolomide: A meta-analysis Xu, Weilin Li, Tao Gao, Liansheng Zheng, Jingwei Shao, Anwen Zhang, Jianmin Oncotarget Meta-Analysis Further treatments are warranted in preventing recurrence or progression for high-grade glioma (HGG) patients having achieved stable disease with tolerable toxicity after the Stupp regimen (6 cycles of temozolomide). This meta-analysis aims to extensively evaluate the safety, feasibility, and efficacy of long-term therapy with temozolomide (>6 cycles) for these patients. We systematically searched the pubmed, Embase and Chinese Biomedical (CBM) databases using the strategy of combination of free-text words and MeSH terms. The efficacy indicators are hazard ratio (HR) for the pooled analysis of overall survival (OS) and progression free survival (PFS). The safety indicator is risk ratio (RR) for the pooled analysis of adverse effects. Six studies comprising a total number of 396 patients met all inclusion and exclusion criteria were included. No heterogeneity and publication bias were observed across each study. It was found that patients could obtain benefits from long-term administration of temozolomide both in OS (HR 2.39, 95% CI 1.82–3.14) and PFS (HR 2.12, 95% CI 1.56–2.89). In addition, the results showed that the patients receiving long-term administration of temozolomide did not experience additional toxicity over that of the Stupp regimen (6 cycles of temozolomide). It could be concluded that it's efficacious and safe for HGG patients to receive long-term therapy with temozolomide. Nevertheless, more randomized controlled trials (RCTs) should be carried out to verify this conclusion. Impact Journals LLC 2017-04-24 /pmc/articles/PMC5584285/ /pubmed/28881684 http://dx.doi.org/10.18632/oncotarget.17401 Text en Copyright: © 2017 Xu et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Meta-Analysis
Xu, Weilin
Li, Tao
Gao, Liansheng
Zheng, Jingwei
Shao, Anwen
Zhang, Jianmin
Efficacy and safety of long-term therapy for high-grade glioma with temozolomide: A meta-analysis
title Efficacy and safety of long-term therapy for high-grade glioma with temozolomide: A meta-analysis
title_full Efficacy and safety of long-term therapy for high-grade glioma with temozolomide: A meta-analysis
title_fullStr Efficacy and safety of long-term therapy for high-grade glioma with temozolomide: A meta-analysis
title_full_unstemmed Efficacy and safety of long-term therapy for high-grade glioma with temozolomide: A meta-analysis
title_short Efficacy and safety of long-term therapy for high-grade glioma with temozolomide: A meta-analysis
title_sort efficacy and safety of long-term therapy for high-grade glioma with temozolomide: a meta-analysis
topic Meta-Analysis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5584285/
https://www.ncbi.nlm.nih.gov/pubmed/28881684
http://dx.doi.org/10.18632/oncotarget.17401
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