Prognostic and predictive molecular biomarkers in advanced colorectal cancer
- PMID: 35780916
- DOI: 10.1016/j.pharmthera.2022.108239
Prognostic and predictive molecular biomarkers in advanced colorectal cancer
Abstract
The revolution of precision medicine has produced unprecedented seismic shifts in the treatment paradigm of advanced cancers. Among the major killers, colorectal cancer (CRC) is far behind the others. In fact, the great successes obtained in breast, NSCLC, melanoma, and genitourinary tract tumors have been observed only in fewer than 5 % metastatic colorectal cancer (mCRC): those with the mismatch repair deficiency (dMMR), a well-known predictive factor for to the outstanding efficacy of checkpoint inhibitors (CPI). The treatment of the remaining vast majority mCRC patients is still based upon only two molecular determinants: the RAS and BRAF mutational status. New promising biomarkers include HER2, tumor mutational burden (TMB) for its possible implications on CPI efficacy, and the extremely rare NTRK fusions. The Consensus Molecular Subtypes classification (CMS) is a good example of the efforts to combine different molecular features of this disease, although its relevance in clinical practice is still under investigation. In this Review, we focus on all these prognostic and predictive biomarkers, analyzing data from the most important clinical trials of the last years. We also try to rank them according to their prognostic and predictive power.
Keywords: BRAF V600E; Checkpoint inhibitors; HER2; Metastatic colorectal cancer; Mismatch repair; Mutational burden.
Copyright © 2022. Published by Elsevier Inc.
Conflict of interest statement
Declaration of Competing Interest AS has received honoraria as speaker and participant to advisory boards by Amgen, Astrazeneca, Bayer, BMS, Lilly, Merck, MSD, Pierre Fabre, Roche, and Servier. AP has received honoraria as speaker by Amgen, Bayer, Lilly, Merck, MSD, Pierre Fabre, and Servier. VM has no conflict of interest to declare.
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