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Biomarkers in the development of individualized treatment regimens for colorectal cancer

INTRODUCTION: Colorectal cancer (CRC) is the third most common and second most deadly malignancy in the world with an estimated 1. 9 million cases and 0.9 million deaths in 2020. The 5-year overall survival for stage I disease is 92% compared to a dismal 11% in stage IV disease. At initial presentat...

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Autores principales: Crutcher, Madison, Waldman, Scott
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9749006/
https://www.ncbi.nlm.nih.gov/pubmed/36530921
http://dx.doi.org/10.3389/fmed.2022.1062423
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author Crutcher, Madison
Waldman, Scott
author_facet Crutcher, Madison
Waldman, Scott
author_sort Crutcher, Madison
collection PubMed
description INTRODUCTION: Colorectal cancer (CRC) is the third most common and second most deadly malignancy in the world with an estimated 1. 9 million cases and 0.9 million deaths in 2020. The 5-year overall survival for stage I disease is 92% compared to a dismal 11% in stage IV disease. At initial presentation, up to 35% of patients have metastatic colorectal cancer (mCRC), and 20–50% of stage II and III patients eventually progress to mCRC. These statistics imply both that there is a proportion of early stage patients who are not receiving adequate treatment and that we are not adequately treating mCRC patients. BODY: Targeted therapies directed at CRC biomarkers are now commonly used in select mCRC patients. In addition to acting as direct targets, these biomarkers also could help stratify which patients receive adjuvant therapies and what types. This review discusses the role of RAS, microsatellite instability, HER2, consensus molecular subtypes and ctDNA/CTC in targeted therapy and adjuvant chemotherapy. DISCUSSION: Given the relatively high recurrence rate in early stage CRC patients as well as the continued poor survival in mCRC patients, additional work needs to be done beyond surgical management to limit recurrence and improve survival. Biomarkers offer both a potential target and a predictive method of stratifying patients to determine those who could benefit from adjuvant treatment.
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spelling pubmed-97490062022-12-15 Biomarkers in the development of individualized treatment regimens for colorectal cancer Crutcher, Madison Waldman, Scott Front Med (Lausanne) Medicine INTRODUCTION: Colorectal cancer (CRC) is the third most common and second most deadly malignancy in the world with an estimated 1. 9 million cases and 0.9 million deaths in 2020. The 5-year overall survival for stage I disease is 92% compared to a dismal 11% in stage IV disease. At initial presentation, up to 35% of patients have metastatic colorectal cancer (mCRC), and 20–50% of stage II and III patients eventually progress to mCRC. These statistics imply both that there is a proportion of early stage patients who are not receiving adequate treatment and that we are not adequately treating mCRC patients. BODY: Targeted therapies directed at CRC biomarkers are now commonly used in select mCRC patients. In addition to acting as direct targets, these biomarkers also could help stratify which patients receive adjuvant therapies and what types. This review discusses the role of RAS, microsatellite instability, HER2, consensus molecular subtypes and ctDNA/CTC in targeted therapy and adjuvant chemotherapy. DISCUSSION: Given the relatively high recurrence rate in early stage CRC patients as well as the continued poor survival in mCRC patients, additional work needs to be done beyond surgical management to limit recurrence and improve survival. Biomarkers offer both a potential target and a predictive method of stratifying patients to determine those who could benefit from adjuvant treatment. Frontiers Media S.A. 2022-11-30 /pmc/articles/PMC9749006/ /pubmed/36530921 http://dx.doi.org/10.3389/fmed.2022.1062423 Text en Copyright © 2022 Crutcher and Waldman. 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 Medicine
Crutcher, Madison
Waldman, Scott
Biomarkers in the development of individualized treatment regimens for colorectal cancer
title Biomarkers in the development of individualized treatment regimens for colorectal cancer
title_full Biomarkers in the development of individualized treatment regimens for colorectal cancer
title_fullStr Biomarkers in the development of individualized treatment regimens for colorectal cancer
title_full_unstemmed Biomarkers in the development of individualized treatment regimens for colorectal cancer
title_short Biomarkers in the development of individualized treatment regimens for colorectal cancer
title_sort biomarkers in the development of individualized treatment regimens for colorectal cancer
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9749006/
https://www.ncbi.nlm.nih.gov/pubmed/36530921
http://dx.doi.org/10.3389/fmed.2022.1062423
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