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Impact of primary tumour location on efficacy of bevacizumab plus chemotherapy in metastatic colorectal cancer
BACKGROUND: Two first-line (1L) bevacizumab trials showed the prognostic value of primary tumour location in metastatic colorectal cancer (mCRC). In this retrospective subgroup analysis, further analysis of the predictive effect of bevacizumab is presented. METHODS: Patients with sidedness informati...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288128/ https://www.ncbi.nlm.nih.gov/pubmed/30487637 http://dx.doi.org/10.1038/s41416-018-0304-6 |
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author | Loupakis, Fotios Hurwitz, Herbert I. Saltz, Leonard Arnold, Dirk Grothey, Axel Nguyen, Quynh Lan Osborne, Stuart Talbot, Jonathan Srock, Stefanie Lenz, Heinz-Josef |
author_facet | Loupakis, Fotios Hurwitz, Herbert I. Saltz, Leonard Arnold, Dirk Grothey, Axel Nguyen, Quynh Lan Osborne, Stuart Talbot, Jonathan Srock, Stefanie Lenz, Heinz-Josef |
author_sort | Loupakis, Fotios |
collection | PubMed |
description | BACKGROUND: Two first-line (1L) bevacizumab trials showed the prognostic value of primary tumour location in metastatic colorectal cancer (mCRC). In this retrospective subgroup analysis, further analysis of the predictive effect of bevacizumab is presented. METHODS: Patients with sidedness information from two randomised phase III studies of bevacizumab + chemotherapy (CT) vs CT as 1L mCRC treatment were analysed retrospectively. RESULTS: Sidedness was determined in 1590 (27% right and 73% left) of 2214 patients. Progression-free survival was improved with bevacizumab + CT vs CT in right-sided (HR = 0.75; 95% CI 0.61, 0.93; p = 0.008) and left-sided (HR = 0.76; 95% CI 0.67, 0.86; p < 0.001) mCRC (pooled analysis). Similarly, overall survival was numerically improved with bevacizumab + CT vs CT in right-sided mCRC (HR = 0.82; 95% CI 0.65, 1.03; p = 0.085), and significantly improved in left-sided mCRC (HR = 0.85; 95% CI 0.74, 0.98; p = 0.028). CONCLUSIONS: This analysis indicates that the effect of bevacizumab is independent of tumour location in mCRC. |
format | Online Article Text |
id | pubmed-6288128 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62881282019-06-21 Impact of primary tumour location on efficacy of bevacizumab plus chemotherapy in metastatic colorectal cancer Loupakis, Fotios Hurwitz, Herbert I. Saltz, Leonard Arnold, Dirk Grothey, Axel Nguyen, Quynh Lan Osborne, Stuart Talbot, Jonathan Srock, Stefanie Lenz, Heinz-Josef Br J Cancer Article BACKGROUND: Two first-line (1L) bevacizumab trials showed the prognostic value of primary tumour location in metastatic colorectal cancer (mCRC). In this retrospective subgroup analysis, further analysis of the predictive effect of bevacizumab is presented. METHODS: Patients with sidedness information from two randomised phase III studies of bevacizumab + chemotherapy (CT) vs CT as 1L mCRC treatment were analysed retrospectively. RESULTS: Sidedness was determined in 1590 (27% right and 73% left) of 2214 patients. Progression-free survival was improved with bevacizumab + CT vs CT in right-sided (HR = 0.75; 95% CI 0.61, 0.93; p = 0.008) and left-sided (HR = 0.76; 95% CI 0.67, 0.86; p < 0.001) mCRC (pooled analysis). Similarly, overall survival was numerically improved with bevacizumab + CT vs CT in right-sided mCRC (HR = 0.82; 95% CI 0.65, 1.03; p = 0.085), and significantly improved in left-sided mCRC (HR = 0.85; 95% CI 0.74, 0.98; p = 0.028). CONCLUSIONS: This analysis indicates that the effect of bevacizumab is independent of tumour location in mCRC. Nature Publishing Group UK 2018-11-29 2018-12-11 /pmc/articles/PMC6288128/ /pubmed/30487637 http://dx.doi.org/10.1038/s41416-018-0304-6 Text en © The Author(s) 2018 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Loupakis, Fotios Hurwitz, Herbert I. Saltz, Leonard Arnold, Dirk Grothey, Axel Nguyen, Quynh Lan Osborne, Stuart Talbot, Jonathan Srock, Stefanie Lenz, Heinz-Josef Impact of primary tumour location on efficacy of bevacizumab plus chemotherapy in metastatic colorectal cancer |
title | Impact of primary tumour location on efficacy of bevacizumab plus chemotherapy in metastatic colorectal cancer |
title_full | Impact of primary tumour location on efficacy of bevacizumab plus chemotherapy in metastatic colorectal cancer |
title_fullStr | Impact of primary tumour location on efficacy of bevacizumab plus chemotherapy in metastatic colorectal cancer |
title_full_unstemmed | Impact of primary tumour location on efficacy of bevacizumab plus chemotherapy in metastatic colorectal cancer |
title_short | Impact of primary tumour location on efficacy of bevacizumab plus chemotherapy in metastatic colorectal cancer |
title_sort | impact of primary tumour location on efficacy of bevacizumab plus chemotherapy in metastatic colorectal cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288128/ https://www.ncbi.nlm.nih.gov/pubmed/30487637 http://dx.doi.org/10.1038/s41416-018-0304-6 |
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