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Precision medicine‐based therapies in advanced colorectal cancer: The University of California San Diego Molecular Tumor Board experience
Treatment for advanced colorectal cancer is often limited by complex molecular profiles, which promote resistance to systemic agents and targeted monotherapies. Recent studies suggest that a personalized, combinatorial approach of matching drugs to tumor alterations may be more effective. We impleme...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9251876/ https://www.ncbi.nlm.nih.gov/pubmed/35238467 http://dx.doi.org/10.1002/1878-0261.13202 |
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author | Louie, Bryan H. Kato, Shumei Kim, Ki Hwan Lim, Hyo Jeong Lee, Suzanna Okamura, Ryosuke Fanta, Paul T. Kurzrock, Razelle |
author_facet | Louie, Bryan H. Kato, Shumei Kim, Ki Hwan Lim, Hyo Jeong Lee, Suzanna Okamura, Ryosuke Fanta, Paul T. Kurzrock, Razelle |
author_sort | Louie, Bryan H. |
collection | PubMed |
description | Treatment for advanced colorectal cancer is often limited by complex molecular profiles, which promote resistance to systemic agents and targeted monotherapies. Recent studies suggest that a personalized, combinatorial approach of matching drugs to tumor alterations may be more effective. We implemented a precision medicine strategy by forming a Molecular Tumor Board (MTB), a multidisciplinary team of clinicians, scientists, bioinformaticians and geneticists. The MTB integrated molecular profiling information and patient characteristics to develop N‐of‐One treatments for 51 patients with advanced colorectal cancer. All patients had metastatic disease and 63% had received ≥ 3 prior therapy lines. Overall, 34/51 patients (67%) were matched to ≥ 1 drug recommended by the MTB based on individual tumor characteristics, whereas 17/51 (33%) patients received unmatched therapies. Patients who received matched therapy demonstrated significantly longer progression‐free survival (hazard ratio [HR], 0.41; 95% confidence interval [CI], 0.21–0.81; P = 0.01) and a trend towards higher clinical benefit rates (41% vs. 18%, P = 0.058) (all multivariate) compared to patients receiving unmatched therapy. The MTB facilitated personalized matching of drugs to tumor characteristics, which was associated with improved progression‐free survival in patients with advanced colorectal cancer. |
format | Online Article Text |
id | pubmed-9251876 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92518762022-07-08 Precision medicine‐based therapies in advanced colorectal cancer: The University of California San Diego Molecular Tumor Board experience Louie, Bryan H. Kato, Shumei Kim, Ki Hwan Lim, Hyo Jeong Lee, Suzanna Okamura, Ryosuke Fanta, Paul T. Kurzrock, Razelle Mol Oncol Research Articles Treatment for advanced colorectal cancer is often limited by complex molecular profiles, which promote resistance to systemic agents and targeted monotherapies. Recent studies suggest that a personalized, combinatorial approach of matching drugs to tumor alterations may be more effective. We implemented a precision medicine strategy by forming a Molecular Tumor Board (MTB), a multidisciplinary team of clinicians, scientists, bioinformaticians and geneticists. The MTB integrated molecular profiling information and patient characteristics to develop N‐of‐One treatments for 51 patients with advanced colorectal cancer. All patients had metastatic disease and 63% had received ≥ 3 prior therapy lines. Overall, 34/51 patients (67%) were matched to ≥ 1 drug recommended by the MTB based on individual tumor characteristics, whereas 17/51 (33%) patients received unmatched therapies. Patients who received matched therapy demonstrated significantly longer progression‐free survival (hazard ratio [HR], 0.41; 95% confidence interval [CI], 0.21–0.81; P = 0.01) and a trend towards higher clinical benefit rates (41% vs. 18%, P = 0.058) (all multivariate) compared to patients receiving unmatched therapy. The MTB facilitated personalized matching of drugs to tumor characteristics, which was associated with improved progression‐free survival in patients with advanced colorectal cancer. John Wiley and Sons Inc. 2022-04-08 2022-07 /pmc/articles/PMC9251876/ /pubmed/35238467 http://dx.doi.org/10.1002/1878-0261.13202 Text en © 2022 The Authors. Molecular Oncology published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Louie, Bryan H. Kato, Shumei Kim, Ki Hwan Lim, Hyo Jeong Lee, Suzanna Okamura, Ryosuke Fanta, Paul T. Kurzrock, Razelle Precision medicine‐based therapies in advanced colorectal cancer: The University of California San Diego Molecular Tumor Board experience |
title | Precision medicine‐based therapies in advanced colorectal cancer: The University of California San Diego Molecular Tumor Board experience |
title_full | Precision medicine‐based therapies in advanced colorectal cancer: The University of California San Diego Molecular Tumor Board experience |
title_fullStr | Precision medicine‐based therapies in advanced colorectal cancer: The University of California San Diego Molecular Tumor Board experience |
title_full_unstemmed | Precision medicine‐based therapies in advanced colorectal cancer: The University of California San Diego Molecular Tumor Board experience |
title_short | Precision medicine‐based therapies in advanced colorectal cancer: The University of California San Diego Molecular Tumor Board experience |
title_sort | precision medicine‐based therapies in advanced colorectal cancer: the university of california san diego molecular tumor board experience |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9251876/ https://www.ncbi.nlm.nih.gov/pubmed/35238467 http://dx.doi.org/10.1002/1878-0261.13202 |
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