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How to Deal with Second Line Dilemma in Metastatic Colorectal Cancer? A Systematic Review and Meta-Analysis

Monoclonal antibodies targeting epidermal growth factor receptor (EGFR) or vascular endothelial growth factor (VEGF) have demonstrated efficacy with chemotherapy (CT) as second line treatment for metastatic colorectal cancer (mCRC). The right sequence of the treatments in all RAS (KRAS/NRAS) wild ty...

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Autores principales: Galvano, Antonio, Incorvaia, Lorena, Badalamenti, Giuseppe, Rizzo, Sergio, Guarini, Aurelia, Cusenza, Stefania, Castellana, Luisa, Barraco, Nadia, Calò, Valentina, Cutaia, Sofia, Currò, Giuseppe, Silvestris, Nicola, Beretta, Giordano Domenico, Bazan, Viviana, Russo, Antonio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6721481/
https://www.ncbi.nlm.nih.gov/pubmed/31443300
http://dx.doi.org/10.3390/cancers11081189
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author Galvano, Antonio
Incorvaia, Lorena
Badalamenti, Giuseppe
Rizzo, Sergio
Guarini, Aurelia
Cusenza, Stefania
Castellana, Luisa
Barraco, Nadia
Calò, Valentina
Cutaia, Sofia
Currò, Giuseppe
Silvestris, Nicola
Beretta, Giordano Domenico
Bazan, Viviana
Russo, Antonio
author_facet Galvano, Antonio
Incorvaia, Lorena
Badalamenti, Giuseppe
Rizzo, Sergio
Guarini, Aurelia
Cusenza, Stefania
Castellana, Luisa
Barraco, Nadia
Calò, Valentina
Cutaia, Sofia
Currò, Giuseppe
Silvestris, Nicola
Beretta, Giordano Domenico
Bazan, Viviana
Russo, Antonio
author_sort Galvano, Antonio
collection PubMed
description Monoclonal antibodies targeting epidermal growth factor receptor (EGFR) or vascular endothelial growth factor (VEGF) have demonstrated efficacy with chemotherapy (CT) as second line treatment for metastatic colorectal cancer (mCRC). The right sequence of the treatments in all RAS (KRAS/NRAS) wild type (wt) patients has not precisely defined. We evaluated the impact of aforementioned targeted therapies in second line setting, analyzing efficacy and safety data from phase III clinical trials. We performed both direct and indirect comparisons between anti-EGFR and anti-VEGF. Outcomes included disease control rate (DCR), objective response rate (ORR), progression-free survival (PFS), overall survival (OS) and G3-G5 toxicities. Our results showed significantly improved OS (HR 0.83, 95% CI 0.72–0.94) and DCR (HR 1.27, 95% CI 1.04–1.54) favouring anti-VEGF combinations in overall population; no statistically significant differences in all RAS wt patients was observed (HR 0.87, 95% CI 0.70–1.09). Anti-EGFR combinations significantly increased ORR in all patients (RR 0.54, 95% CI 0.31–0.96), showing a trend also in all RAS wt patients (RR 0.63, 95% CI 0.48–0.83). No significant difference in PFS and DCR all RAS was registered. Our results provided for the first time a strong rationale to manage both targeted agents in second line setting.
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spelling pubmed-67214812019-09-10 How to Deal with Second Line Dilemma in Metastatic Colorectal Cancer? A Systematic Review and Meta-Analysis Galvano, Antonio Incorvaia, Lorena Badalamenti, Giuseppe Rizzo, Sergio Guarini, Aurelia Cusenza, Stefania Castellana, Luisa Barraco, Nadia Calò, Valentina Cutaia, Sofia Currò, Giuseppe Silvestris, Nicola Beretta, Giordano Domenico Bazan, Viviana Russo, Antonio Cancers (Basel) Review Monoclonal antibodies targeting epidermal growth factor receptor (EGFR) or vascular endothelial growth factor (VEGF) have demonstrated efficacy with chemotherapy (CT) as second line treatment for metastatic colorectal cancer (mCRC). The right sequence of the treatments in all RAS (KRAS/NRAS) wild type (wt) patients has not precisely defined. We evaluated the impact of aforementioned targeted therapies in second line setting, analyzing efficacy and safety data from phase III clinical trials. We performed both direct and indirect comparisons between anti-EGFR and anti-VEGF. Outcomes included disease control rate (DCR), objective response rate (ORR), progression-free survival (PFS), overall survival (OS) and G3-G5 toxicities. Our results showed significantly improved OS (HR 0.83, 95% CI 0.72–0.94) and DCR (HR 1.27, 95% CI 1.04–1.54) favouring anti-VEGF combinations in overall population; no statistically significant differences in all RAS wt patients was observed (HR 0.87, 95% CI 0.70–1.09). Anti-EGFR combinations significantly increased ORR in all patients (RR 0.54, 95% CI 0.31–0.96), showing a trend also in all RAS wt patients (RR 0.63, 95% CI 0.48–0.83). No significant difference in PFS and DCR all RAS was registered. Our results provided for the first time a strong rationale to manage both targeted agents in second line setting. MDPI 2019-08-15 /pmc/articles/PMC6721481/ /pubmed/31443300 http://dx.doi.org/10.3390/cancers11081189 Text en © 2019 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 Review
Galvano, Antonio
Incorvaia, Lorena
Badalamenti, Giuseppe
Rizzo, Sergio
Guarini, Aurelia
Cusenza, Stefania
Castellana, Luisa
Barraco, Nadia
Calò, Valentina
Cutaia, Sofia
Currò, Giuseppe
Silvestris, Nicola
Beretta, Giordano Domenico
Bazan, Viviana
Russo, Antonio
How to Deal with Second Line Dilemma in Metastatic Colorectal Cancer? A Systematic Review and Meta-Analysis
title How to Deal with Second Line Dilemma in Metastatic Colorectal Cancer? A Systematic Review and Meta-Analysis
title_full How to Deal with Second Line Dilemma in Metastatic Colorectal Cancer? A Systematic Review and Meta-Analysis
title_fullStr How to Deal with Second Line Dilemma in Metastatic Colorectal Cancer? A Systematic Review and Meta-Analysis
title_full_unstemmed How to Deal with Second Line Dilemma in Metastatic Colorectal Cancer? A Systematic Review and Meta-Analysis
title_short How to Deal with Second Line Dilemma in Metastatic Colorectal Cancer? A Systematic Review and Meta-Analysis
title_sort how to deal with second line dilemma in metastatic colorectal cancer? a systematic review and meta-analysis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6721481/
https://www.ncbi.nlm.nih.gov/pubmed/31443300
http://dx.doi.org/10.3390/cancers11081189
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