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Magnitude of risks and benefits of the addition of bevacizumab to chemotherapy for advanced breast cancer patients: Meta-regression analysis of randomized trials
BACKGROUND: Although the addition of bevacizumab significantly improves the efficacy of chemotherapy for advanced breast cancer, regulatory concerns still exist with regard to the magnitude of the benefits and the overall safety profile. METHODS: A literature-based meta-analysis to quantify the magn...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3120715/ https://www.ncbi.nlm.nih.gov/pubmed/21569417 http://dx.doi.org/10.1186/1756-9966-30-54 |
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author | Cuppone, Federica Bria, Emilio Vaccaro, Vanja Puglisi, Fabio Fabi, Alessandra Sperduti, Isabella Carlini, Paolo Milella, Michele Nisticò, Cecilia Russillo, Michelangelo Papaldo, Paola Ferretti, Gianluigi Aapro, Matti Giannarelli, Diana Cognetti, Francesco |
author_facet | Cuppone, Federica Bria, Emilio Vaccaro, Vanja Puglisi, Fabio Fabi, Alessandra Sperduti, Isabella Carlini, Paolo Milella, Michele Nisticò, Cecilia Russillo, Michelangelo Papaldo, Paola Ferretti, Gianluigi Aapro, Matti Giannarelli, Diana Cognetti, Francesco |
author_sort | Cuppone, Federica |
collection | PubMed |
description | BACKGROUND: Although the addition of bevacizumab significantly improves the efficacy of chemotherapy for advanced breast cancer, regulatory concerns still exist with regard to the magnitude of the benefits and the overall safety profile. METHODS: A literature-based meta-analysis to quantify the magnitude of benefit and safety of adding bevacizumab to chemotherapy for advanced breast cancer patients was conducted. Meta-regression and sensitivity analyses were also performed to identify additional predictors of outcome and to assess the influence of trial design. RESULTS: Five trials (3,841 patients) were gathered. A significant interaction according to treatment line was found for progression-free survival (PFS, p = 0.027); PFS was significantly improved for 1(st )line (Hazard Ratio, HR 0.68, p < 0.0001), with a 1-yr absolute difference (AD) of 8.4% (number needed to treat, NNT 12). A non-significant trend was found in overall survival (OS), and in PFS for 2(nd )line. Responses were improved with the addition of bevacizumab, without interaction between 1(st )line (Relative Risk, RR 1.46, p < 0.0001) and 2(nd )line (RR 1.58, p = 0.05). The most important toxicity was hypertension, accounting for a significant AD of 4.5% against bevacizumab (number needed to harm, NNH 22). Other significant, although less clinically meaningful, adverse events were proteinuria, neurotoxicity, febrile neutropenia, and bleeding. At the meta-regression analysis for 1(st)-line, more than 3 metastatic sites (p = 0.032), no adjuvant chemotherapy (p = 0.00013), negative hormonal receptor status (p = 0.009), and prior anthracyclines-exposure (p = 0.019), did significantly affect PFS. CONCLUSIONS: Although with heterogeneity, the addition of bevacizumab to 1(st)-line chemotherapy significantly improves PFS, and overall activity. Hypertension should be weighted with the overall benefit on the individual basis. |
format | Online Article Text |
id | pubmed-3120715 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-31207152011-06-23 Magnitude of risks and benefits of the addition of bevacizumab to chemotherapy for advanced breast cancer patients: Meta-regression analysis of randomized trials Cuppone, Federica Bria, Emilio Vaccaro, Vanja Puglisi, Fabio Fabi, Alessandra Sperduti, Isabella Carlini, Paolo Milella, Michele Nisticò, Cecilia Russillo, Michelangelo Papaldo, Paola Ferretti, Gianluigi Aapro, Matti Giannarelli, Diana Cognetti, Francesco J Exp Clin Cancer Res Research BACKGROUND: Although the addition of bevacizumab significantly improves the efficacy of chemotherapy for advanced breast cancer, regulatory concerns still exist with regard to the magnitude of the benefits and the overall safety profile. METHODS: A literature-based meta-analysis to quantify the magnitude of benefit and safety of adding bevacizumab to chemotherapy for advanced breast cancer patients was conducted. Meta-regression and sensitivity analyses were also performed to identify additional predictors of outcome and to assess the influence of trial design. RESULTS: Five trials (3,841 patients) were gathered. A significant interaction according to treatment line was found for progression-free survival (PFS, p = 0.027); PFS was significantly improved for 1(st )line (Hazard Ratio, HR 0.68, p < 0.0001), with a 1-yr absolute difference (AD) of 8.4% (number needed to treat, NNT 12). A non-significant trend was found in overall survival (OS), and in PFS for 2(nd )line. Responses were improved with the addition of bevacizumab, without interaction between 1(st )line (Relative Risk, RR 1.46, p < 0.0001) and 2(nd )line (RR 1.58, p = 0.05). The most important toxicity was hypertension, accounting for a significant AD of 4.5% against bevacizumab (number needed to harm, NNH 22). Other significant, although less clinically meaningful, adverse events were proteinuria, neurotoxicity, febrile neutropenia, and bleeding. At the meta-regression analysis for 1(st)-line, more than 3 metastatic sites (p = 0.032), no adjuvant chemotherapy (p = 0.00013), negative hormonal receptor status (p = 0.009), and prior anthracyclines-exposure (p = 0.019), did significantly affect PFS. CONCLUSIONS: Although with heterogeneity, the addition of bevacizumab to 1(st)-line chemotherapy significantly improves PFS, and overall activity. Hypertension should be weighted with the overall benefit on the individual basis. BioMed Central 2011-05-12 /pmc/articles/PMC3120715/ /pubmed/21569417 http://dx.doi.org/10.1186/1756-9966-30-54 Text en Copyright ©2011 Cuppone 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. |
spellingShingle | Research Cuppone, Federica Bria, Emilio Vaccaro, Vanja Puglisi, Fabio Fabi, Alessandra Sperduti, Isabella Carlini, Paolo Milella, Michele Nisticò, Cecilia Russillo, Michelangelo Papaldo, Paola Ferretti, Gianluigi Aapro, Matti Giannarelli, Diana Cognetti, Francesco Magnitude of risks and benefits of the addition of bevacizumab to chemotherapy for advanced breast cancer patients: Meta-regression analysis of randomized trials |
title | Magnitude of risks and benefits of the addition of bevacizumab to chemotherapy for advanced breast cancer patients: Meta-regression analysis of randomized trials |
title_full | Magnitude of risks and benefits of the addition of bevacizumab to chemotherapy for advanced breast cancer patients: Meta-regression analysis of randomized trials |
title_fullStr | Magnitude of risks and benefits of the addition of bevacizumab to chemotherapy for advanced breast cancer patients: Meta-regression analysis of randomized trials |
title_full_unstemmed | Magnitude of risks and benefits of the addition of bevacizumab to chemotherapy for advanced breast cancer patients: Meta-regression analysis of randomized trials |
title_short | Magnitude of risks and benefits of the addition of bevacizumab to chemotherapy for advanced breast cancer patients: Meta-regression analysis of randomized trials |
title_sort | magnitude of risks and benefits of the addition of bevacizumab to chemotherapy for advanced breast cancer patients: meta-regression analysis of randomized trials |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3120715/ https://www.ncbi.nlm.nih.gov/pubmed/21569417 http://dx.doi.org/10.1186/1756-9966-30-54 |
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