Microsatellite Instable Colorectal Adenocarcinoma Diagnostics: The Advent of Liquid Biopsy Approaches.

cancer screening circulating tumor DNA colorectal cancer early detection immunotherapy liquid biopsy microsatellite Instability

Journal

Frontiers in oncology
ISSN: 2234-943X
Titre abrégé: Front Oncol
Pays: Switzerland
ID NLM: 101568867

Informations de publication

Date de publication:
2022
Historique:
received: 27 04 2022
accepted: 30 05 2022
entrez: 15 7 2022
pubmed: 16 7 2022
medline: 16 7 2022
Statut: epublish

Résumé

The introduction of immunotherapy has revolutionized the oncological targeted therapy paradigm. Microsatellite instability (MSI) identifies a subgroup of colorectal cancers (CRCs) which respond to treatment with immune checkpoint inhibitors. Tissue biopsy is currently the gold standard for the assessment of MSI/Mismatch Repair deficiency (MMRd) by means immunohistochemistry or molecular assays. However, the application of liquid biopsy in the clinic may help to overcome several limitations of tissue analysis and may provide great benefit to the diagnostic scenario and therapeutic decision-making process. In the context of MSI/MMRd CRC, the use of liquid biopsy may allow to establish MSI/MMR status if tissue sampling cannot be performed or in case of discordant tissue biopsies. Liquid biopsy may also become a powerful tool to monitor treatment response and the onset resistance to immunotherapy over time and to stratify of MSI/MMRd patients according to their risk of relapse and metastases. The aim of this review is to summarize the main technical aspects and clinical applications, the benefits, and limitations of the use of liquid biopsy in MSI/MMRd colorectal cancer patients.

Identifiants

pubmed: 35837109
doi: 10.3389/fonc.2022.930108
pmc: PMC9273960
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

930108

Informations de copyright

Copyright © 2022 Ceccon, Angerilli, Rasola, Procaccio, Sabbadin, Bergamo, Malapelle, Lonardi and Fassan.

Déclaration de conflit d'intérêts

UM has received personal fees (as consultant and/or speaker bureau) from Boehringer Ingelheim, Roche, MSD, Amgen, ThermoFisher Scientifics, Eli Lilly, Diaceutics, GSK, Merck, and AstraZeneca, Jannseen unrelated to the current work. SL has received personal fees for consulting or advisory role from Amgen, Merck Serono, Lilly, Astra Zeneca, Incyte, Daiichi-Sankyo, Bristol-Myers Squibb, Servier, MSD, Roche, Pierre-Fabre, and GSK, and receiving research grants from Amgen, Merck Serono, Bayer, Roche, Lilly, Astra Zeneca, and Bristol-Myers Squibb, unrelated to the current work. Matteo Fassan received research funding from Astellas Pharma, Macrophage Pharma and QED Therapeutics and had roles as consultant or advisor for Astellas Pharma, Roche, Astra Zeneca, MSD and GSK-Tesaro, unrelated to the current work. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Carlotta Ceccon (C)

Department of Medicine (DIMED), University of Padua, Padua, Italy.

Valentina Angerilli (V)

Department of Medicine (DIMED), University of Padua, Padua, Italy.

Cosimo Rasola (C)

Veneto Institute of Oncology, IOV-IRCCS, Padua, Italy.
Department of Surgery, Oncology and Gastroenterology, University of Padua, Padua, Italy.

Letizia Procaccio (L)

Veneto Institute of Oncology, IOV-IRCCS, Padua, Italy.

Marianna Sabbadin (M)

Veneto Institute of Oncology, IOV-IRCCS, Padua, Italy.

Francesca Bergamo (F)

Veneto Institute of Oncology, IOV-IRCCS, Padua, Italy.

Umberto Malapelle (U)

Department of Public Health, University of Naples Federico II, Naples, Italy.

Sara Lonardi (S)

Veneto Institute of Oncology, IOV-IRCCS, Padua, Italy.

Matteo Fassan (M)

Department of Medicine (DIMED), University of Padua, Padua, Italy.
Veneto Institute of Oncology, IOV-IRCCS, Padua, Italy.

Classifications MeSH