Dynamics of RAS Mutations in Liquid Biopsies in Metastatic Colorectal Cancer Patients—Case Series and Literature Review

Author:

Popescu Ionut1ORCID,Croitoru Vlad M.12ORCID,Croitoru-Cazacu Irina M.23ORCID,Dudau Ana-Maria12,Herlea Vlad34,Dima Simona Olimpia35ORCID,Croitoru Adina Emilia2ORCID

Affiliation:

1. Faculty of Medicine, Titu Maiorescu University, 031593 Bucharest, Romania

2. Department of Oncology, Fundeni Clinical Institute, 022328 Bucharest, Romania

3. Faculty of Medicine, Carol Davila University of Medicine and Pharmacy, 020021 Bucharest, Romania

4. Department of Pathology, Fundeni Clinical Institute, 022328 Bucharest, Romania

5. Center of Excellence in Translational Medicine, Fundeni Clinical Institute, 022328 Bucharest, Romania

Abstract

Liquid biopsies can accurately identify molecular alterations in patients with colorectal cancer with high concordance with tissue analysis and shorter turnaround times. Circulating tumor (ct) DNA analysis can be used for diagnosing and monitoring tumor evolution in patients with metastatic colorectal cancer who are treated with EGFR inhibitors. In this article, we reported three clinical cases to illustrate the relevance of RAS mutations identified in ctDNA samples of patients with wild-type metastatic colorectal cancer who received an EGFR inhibitor plus chemotherapy as first-line treatment. The identification of RAS mutations in these patients is one of the most frequently identified mechanisms of acquired resistance. However, detecting a KRAS mutation via liquid biopsy can be caused by inter-tumor heterogeneity or it can be a false positive due to clonal hematopoiesis. More research is needed to determine whether ctDNA monitoring may help guide therapy options in metastatic colorectal cancer patients. We performed a literature review to assess the technologies that are used for analysis of RAS mutations on ctDNA, the degree of agreement between tissue and plasma and the importance of tissue/plasma discordant cases.

Publisher

MDPI AG

Reference61 articles.

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