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The Role of Anti-Angiogenics in Pre-Treated Metastatic BRAF-Mutant Colorectal Cancer: A Pooled Analysis
Background. FOLFOXIRI plus Bevacizumab is one of the most frequently used first-line treatments for patients with BRAF-mutant colorectal cancer (CRC), while second-line treatment requires extensive further research. In this pooled analysis, we evaluate the impact of anti-angiogenics in patients with...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7226019/ https://www.ncbi.nlm.nih.gov/pubmed/32326305 http://dx.doi.org/10.3390/cancers12041022 |
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author | Gelsomino, Fabio Casadei-Gardini, Andrea Rossini, Daniele Boccaccino, Alessandra Masi, Gianluca Cremolini, Chiara Spallanzani, Andrea Viola, Massimo Giuseppe Garajovà, Ingrid Salati, Massimiliano Elia, Maria Teresa Caputo, Francesco Santini, Chiara Falcone, Alfredo Cascinu, Stefano Tamburini, Emiliano |
author_facet | Gelsomino, Fabio Casadei-Gardini, Andrea Rossini, Daniele Boccaccino, Alessandra Masi, Gianluca Cremolini, Chiara Spallanzani, Andrea Viola, Massimo Giuseppe Garajovà, Ingrid Salati, Massimiliano Elia, Maria Teresa Caputo, Francesco Santini, Chiara Falcone, Alfredo Cascinu, Stefano Tamburini, Emiliano |
author_sort | Gelsomino, Fabio |
collection | PubMed |
description | Background. FOLFOXIRI plus Bevacizumab is one of the most frequently used first-line treatments for patients with BRAF-mutant colorectal cancer (CRC), while second-line treatment requires extensive further research. In this pooled analysis, we evaluate the impact of anti-angiogenics in patients with pre-treated BRAF-mutant CRC. Methods. We monitored patients in randomized, controlled studies who had advanced CRC and were undergoing second-line chemotherapy in addition to utilizing Bevacizumab, Ramucirumab or Aflibercept treatments. These data were pooled together with the data and results of BRAF-mutant patients enrolled in two phase III trials (TRIBE and TRIBE-2 study), who had been treated with second-line treatment both with or without Bevacizumab. Overall survival (OS), in relation to BRAF mutational status, was the primary focus. Results. Pooled analysis included 129 patients. Anti-angiogenics were found to have a significant advantage over the placebo in terms of OS (HR 0.50, 95%CI 0.29–0.85) (p = 0.01). Conclusions. Our pooled analysis confirms the efficacy of anti-angiogenics in pre-treated BRAF-mutant CRC, establishing the combination of chemotherapy plus Bevacizumab or Ramucirumab or Aflibercept as a valid treatment option. |
format | Online Article Text |
id | pubmed-7226019 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-72260192020-05-18 The Role of Anti-Angiogenics in Pre-Treated Metastatic BRAF-Mutant Colorectal Cancer: A Pooled Analysis Gelsomino, Fabio Casadei-Gardini, Andrea Rossini, Daniele Boccaccino, Alessandra Masi, Gianluca Cremolini, Chiara Spallanzani, Andrea Viola, Massimo Giuseppe Garajovà, Ingrid Salati, Massimiliano Elia, Maria Teresa Caputo, Francesco Santini, Chiara Falcone, Alfredo Cascinu, Stefano Tamburini, Emiliano Cancers (Basel) Article Background. FOLFOXIRI plus Bevacizumab is one of the most frequently used first-line treatments for patients with BRAF-mutant colorectal cancer (CRC), while second-line treatment requires extensive further research. In this pooled analysis, we evaluate the impact of anti-angiogenics in patients with pre-treated BRAF-mutant CRC. Methods. We monitored patients in randomized, controlled studies who had advanced CRC and were undergoing second-line chemotherapy in addition to utilizing Bevacizumab, Ramucirumab or Aflibercept treatments. These data were pooled together with the data and results of BRAF-mutant patients enrolled in two phase III trials (TRIBE and TRIBE-2 study), who had been treated with second-line treatment both with or without Bevacizumab. Overall survival (OS), in relation to BRAF mutational status, was the primary focus. Results. Pooled analysis included 129 patients. Anti-angiogenics were found to have a significant advantage over the placebo in terms of OS (HR 0.50, 95%CI 0.29–0.85) (p = 0.01). Conclusions. Our pooled analysis confirms the efficacy of anti-angiogenics in pre-treated BRAF-mutant CRC, establishing the combination of chemotherapy plus Bevacizumab or Ramucirumab or Aflibercept as a valid treatment option. MDPI 2020-04-21 /pmc/articles/PMC7226019/ /pubmed/32326305 http://dx.doi.org/10.3390/cancers12041022 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Gelsomino, Fabio Casadei-Gardini, Andrea Rossini, Daniele Boccaccino, Alessandra Masi, Gianluca Cremolini, Chiara Spallanzani, Andrea Viola, Massimo Giuseppe Garajovà, Ingrid Salati, Massimiliano Elia, Maria Teresa Caputo, Francesco Santini, Chiara Falcone, Alfredo Cascinu, Stefano Tamburini, Emiliano The Role of Anti-Angiogenics in Pre-Treated Metastatic BRAF-Mutant Colorectal Cancer: A Pooled Analysis |
title | The Role of Anti-Angiogenics in Pre-Treated Metastatic BRAF-Mutant Colorectal Cancer: A Pooled Analysis |
title_full | The Role of Anti-Angiogenics in Pre-Treated Metastatic BRAF-Mutant Colorectal Cancer: A Pooled Analysis |
title_fullStr | The Role of Anti-Angiogenics in Pre-Treated Metastatic BRAF-Mutant Colorectal Cancer: A Pooled Analysis |
title_full_unstemmed | The Role of Anti-Angiogenics in Pre-Treated Metastatic BRAF-Mutant Colorectal Cancer: A Pooled Analysis |
title_short | The Role of Anti-Angiogenics in Pre-Treated Metastatic BRAF-Mutant Colorectal Cancer: A Pooled Analysis |
title_sort | role of anti-angiogenics in pre-treated metastatic braf-mutant colorectal cancer: a pooled analysis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7226019/ https://www.ncbi.nlm.nih.gov/pubmed/32326305 http://dx.doi.org/10.3390/cancers12041022 |
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