Cell-Free DNA as a Surveillance Tool for Hepatocellular Carcinoma Patients after Liver Transplant

Author:

Manzi Joao12,Hoff Camilla O.12ORCID,Ferreira Raphaella2ORCID,Glehn-Ponsirenas Renata3ORCID,Selvaggi Gennaro2ORCID,Tekin Akin2,O’Brien Christopher B.2,Feun Lynn2,Vianna Rodrigo2ORCID,Abreu Phillipe2ORCID

Affiliation:

1. School of Medicine, University of Sao Paulo, Sao Paulo 05508-900, Brazil

2. Miami Transplant Institute, Jackson Memorial Hospital, University of Miami, Miami, FL 33136, USA

3. Medical Affairs Department, CareDx, Inc., Brisbane, CA 94005, USA

Abstract

The liver is the world’s sixth most common primary tumor site, responsible for approximately 5% of all cancers and over 8% of cancer-related deaths. Hepatocellular carcinoma (HCC) is the predominant type of liver cancer, accounting for approximately 75% of all primary liver tumors. A major therapeutic tool for this disease is liver transplantation. Two of the most significant issues in treating HCC are tumor recurrence and graft rejection. Currently, the detection and monitoring of HCC recurrence and graft rejection mainly consist of imaging methods, tissue biopsies, and alpha-fetoprotein (AFP) follow-up. However, they have limited accuracy and precision. One of the many possible components of cfDNA is circulating tumor DNA (ctDNA), which is cfDNA derived from tumor cells. Another important component in transplantation is donor-derived cfDNA (dd-cfDNA), derived from donor tissue. All the components of cfDNA can be analyzed in blood samples as liquid biopsies. These can play a role in determining prognosis, tumor recurrence, and graft rejection, assisting in an overall manner in clinical decision-making in the treatment of HCC.

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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