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Bcl-2 expression predicts sensitivity to chemotherapy in breast cancer: a systematic review and meta-analysis
BACKGROUND: Numerous studies have yielded inconclusive results regarding the relationship between anti-apoptotic protein Bcl-2 expression and the sensitivity to chemotherapy in the patients with breast cancer. The purpose of the current study was therefore to elaborate their relationship. METHODS, F...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3922829/ https://www.ncbi.nlm.nih.gov/pubmed/24370277 http://dx.doi.org/10.1186/1756-9966-32-105 |
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author | Yang, Dong Chen, Min-Bin Wang, Li-Qiang Yang, Lan Liu, Chao-Ying Lu, Pei-Hua |
author_facet | Yang, Dong Chen, Min-Bin Wang, Li-Qiang Yang, Lan Liu, Chao-Ying Lu, Pei-Hua |
author_sort | Yang, Dong |
collection | PubMed |
description | BACKGROUND: Numerous studies have yielded inconclusive results regarding the relationship between anti-apoptotic protein Bcl-2 expression and the sensitivity to chemotherapy in the patients with breast cancer. The purpose of the current study was therefore to elaborate their relationship. METHODS, FINDINGS: A total of 23 previously published eligible studies involving 2,467 cases were identified and included in this meta-analysis. Negative Bcl-2 expression was associated with good chemotherapy response in breast cancer patients (total objective response [OR]: risk ratio [RR] = 1.16, 95% confidence interval [CI] = 1.02-1.32, p = 0.026; total complete response [CR]: RR = 1.67, 95% CI = 1.24-2.24, p = 0.001; pathological CR: RR = 1.92, 95% CI = 1.38-2.69, p < 0.001). In further stratified analyses, this association remained for sub-groups of response in neoadjuvant chemotherapy setting, especially pathological CR. Besides, negative Bcl-2 expression was significantly associated with good OR and pathological CR in anthracycline-based chemotherapy subgroup. Furthermore, there were significant links between negative Bcl-2 expression and taxane-based chemotherapy with pathological CR, but not OR. CONCLUSION: The results of the present meta-analysis suggest that Bcl-2 expression is a predictive factor for chemotherapy sensitivity in breast cancer patients. They could also potentially benefit further clinical treatment for breast cancers. |
format | Online Article Text |
id | pubmed-3922829 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-39228292014-02-13 Bcl-2 expression predicts sensitivity to chemotherapy in breast cancer: a systematic review and meta-analysis Yang, Dong Chen, Min-Bin Wang, Li-Qiang Yang, Lan Liu, Chao-Ying Lu, Pei-Hua J Exp Clin Cancer Res Review BACKGROUND: Numerous studies have yielded inconclusive results regarding the relationship between anti-apoptotic protein Bcl-2 expression and the sensitivity to chemotherapy in the patients with breast cancer. The purpose of the current study was therefore to elaborate their relationship. METHODS, FINDINGS: A total of 23 previously published eligible studies involving 2,467 cases were identified and included in this meta-analysis. Negative Bcl-2 expression was associated with good chemotherapy response in breast cancer patients (total objective response [OR]: risk ratio [RR] = 1.16, 95% confidence interval [CI] = 1.02-1.32, p = 0.026; total complete response [CR]: RR = 1.67, 95% CI = 1.24-2.24, p = 0.001; pathological CR: RR = 1.92, 95% CI = 1.38-2.69, p < 0.001). In further stratified analyses, this association remained for sub-groups of response in neoadjuvant chemotherapy setting, especially pathological CR. Besides, negative Bcl-2 expression was significantly associated with good OR and pathological CR in anthracycline-based chemotherapy subgroup. Furthermore, there were significant links between negative Bcl-2 expression and taxane-based chemotherapy with pathological CR, but not OR. CONCLUSION: The results of the present meta-analysis suggest that Bcl-2 expression is a predictive factor for chemotherapy sensitivity in breast cancer patients. They could also potentially benefit further clinical treatment for breast cancers. BioMed Central 2013-12-27 /pmc/articles/PMC3922829/ /pubmed/24370277 http://dx.doi.org/10.1186/1756-9966-32-105 Text en Copyright © 2013 Yang et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Review Yang, Dong Chen, Min-Bin Wang, Li-Qiang Yang, Lan Liu, Chao-Ying Lu, Pei-Hua Bcl-2 expression predicts sensitivity to chemotherapy in breast cancer: a systematic review and meta-analysis |
title | Bcl-2 expression predicts sensitivity to chemotherapy in breast cancer: a systematic review and meta-analysis |
title_full | Bcl-2 expression predicts sensitivity to chemotherapy in breast cancer: a systematic review and meta-analysis |
title_fullStr | Bcl-2 expression predicts sensitivity to chemotherapy in breast cancer: a systematic review and meta-analysis |
title_full_unstemmed | Bcl-2 expression predicts sensitivity to chemotherapy in breast cancer: a systematic review and meta-analysis |
title_short | Bcl-2 expression predicts sensitivity to chemotherapy in breast cancer: a systematic review and meta-analysis |
title_sort | bcl-2 expression predicts sensitivity to chemotherapy in breast cancer: a systematic review and meta-analysis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3922829/ https://www.ncbi.nlm.nih.gov/pubmed/24370277 http://dx.doi.org/10.1186/1756-9966-32-105 |
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