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Molecular targeted therapy for metastatic colorectal cancer: current and evolving approaches
Colorectal cancer (CRC) represents 10% of all cancer types, making it the third leading cause of cancer-related deaths globally. Metastasis is the primary factor causing mortality in CRC patients. Approximately 22% of CRC-related deaths have metastasis present at diagnosis, with approximately 70% of...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10622804/ https://www.ncbi.nlm.nih.gov/pubmed/37927605 http://dx.doi.org/10.3389/fphar.2023.1165666 |
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author | Li, Furong Lin, Yanping Li, Rong Shen, Xin Xiang, Mengying Xiong, Guangrui Zhang, Ke Xia, Tingrong Guo, Jiangyan Miao, Zhonghui Liao, Yedan Zhang, Xuan Xie, Lin |
author_facet | Li, Furong Lin, Yanping Li, Rong Shen, Xin Xiang, Mengying Xiong, Guangrui Zhang, Ke Xia, Tingrong Guo, Jiangyan Miao, Zhonghui Liao, Yedan Zhang, Xuan Xie, Lin |
author_sort | Li, Furong |
collection | PubMed |
description | Colorectal cancer (CRC) represents 10% of all cancer types, making it the third leading cause of cancer-related deaths globally. Metastasis is the primary factor causing mortality in CRC patients. Approximately 22% of CRC-related deaths have metastasis present at diagnosis, with approximately 70% of these cases recurring. Recently, with the application of novel targeted drugs, targeted therapy has become the first-line option for individualized and comprehensive treatment of CRC. The management of these patients remains a significant medical challenge. The most prevalent targeted therapies for CRC in clinical practice focus on anti-vascular endothelial growth factor and its receptor, epidermal growth factor receptor (EGFR), and multi-target kinase inhibitors. In the wake of advancements in precision diagnosis and widespread adoption of second-generation sequencing (NGS) technology, rare targets such as BRAF V600E mutation, KRAS mutation, HER2 overexpression/amplification, and MSI-H/dMMR in metastatic colorectal cancer (mCRC) are increasingly being discovered. Simultaneously, new therapeutic drugs targeting these mutations are being actively investigated. This article reviews the progress in clinical research for developing targeted therapeutics for CRC, in light of advances in precision medicine and discovery of new molecular target drugs. |
format | Online Article Text |
id | pubmed-10622804 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-106228042023-11-04 Molecular targeted therapy for metastatic colorectal cancer: current and evolving approaches Li, Furong Lin, Yanping Li, Rong Shen, Xin Xiang, Mengying Xiong, Guangrui Zhang, Ke Xia, Tingrong Guo, Jiangyan Miao, Zhonghui Liao, Yedan Zhang, Xuan Xie, Lin Front Pharmacol Pharmacology Colorectal cancer (CRC) represents 10% of all cancer types, making it the third leading cause of cancer-related deaths globally. Metastasis is the primary factor causing mortality in CRC patients. Approximately 22% of CRC-related deaths have metastasis present at diagnosis, with approximately 70% of these cases recurring. Recently, with the application of novel targeted drugs, targeted therapy has become the first-line option for individualized and comprehensive treatment of CRC. The management of these patients remains a significant medical challenge. The most prevalent targeted therapies for CRC in clinical practice focus on anti-vascular endothelial growth factor and its receptor, epidermal growth factor receptor (EGFR), and multi-target kinase inhibitors. In the wake of advancements in precision diagnosis and widespread adoption of second-generation sequencing (NGS) technology, rare targets such as BRAF V600E mutation, KRAS mutation, HER2 overexpression/amplification, and MSI-H/dMMR in metastatic colorectal cancer (mCRC) are increasingly being discovered. Simultaneously, new therapeutic drugs targeting these mutations are being actively investigated. This article reviews the progress in clinical research for developing targeted therapeutics for CRC, in light of advances in precision medicine and discovery of new molecular target drugs. Frontiers Media S.A. 2023-10-20 /pmc/articles/PMC10622804/ /pubmed/37927605 http://dx.doi.org/10.3389/fphar.2023.1165666 Text en Copyright © 2023 Li, Lin, Li, Shen, Xiang, Xiong, Zhang, Xia, Guo, Miao, Liao, Zhang and Xie. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology Li, Furong Lin, Yanping Li, Rong Shen, Xin Xiang, Mengying Xiong, Guangrui Zhang, Ke Xia, Tingrong Guo, Jiangyan Miao, Zhonghui Liao, Yedan Zhang, Xuan Xie, Lin Molecular targeted therapy for metastatic colorectal cancer: current and evolving approaches |
title | Molecular targeted therapy for metastatic colorectal cancer: current and evolving approaches |
title_full | Molecular targeted therapy for metastatic colorectal cancer: current and evolving approaches |
title_fullStr | Molecular targeted therapy for metastatic colorectal cancer: current and evolving approaches |
title_full_unstemmed | Molecular targeted therapy for metastatic colorectal cancer: current and evolving approaches |
title_short | Molecular targeted therapy for metastatic colorectal cancer: current and evolving approaches |
title_sort | molecular targeted therapy for metastatic colorectal cancer: current and evolving approaches |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10622804/ https://www.ncbi.nlm.nih.gov/pubmed/37927605 http://dx.doi.org/10.3389/fphar.2023.1165666 |
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