Literature DB >> 33582128

Antiviral therapy in the palliative setting of HCC (BCLC-B and -C).

Maria Reig1, Giuseppe Cabibbo2.   

Abstract

The potential impact of direct-acting antivirals (DAAs) in patients with Barcelona Clinic Liver Cancer (BCLC)-B/C stage hepatocellular carcinoma (HCC) is understudied. Patients with HCC have been systematically excluded from randomised controlled trials evaluating the effectiveness of DAAs. Thus, the benefits of DAAs in patients with HCC are less well defined. The presence of active HCC before the initiation of DAA treatment is reported to be a predictor of DAA failure, and studies in patients without HCC have demonstrated that improvements in cirrhosis complications were lower or absent after DAA failure. Even if viral eradication is achieved using DAAs, reversal of liver function impairment may take longer than the development of end-stage cancer status. Additionally, the impact of DAAs on HCC recurrence is still a controversial topic. Thus, the decision of whether to use DAAs should be made on a patient-by-patient basis, and each patient should be informed of all the potential risks and benefits associated with their usage. This document summarises the current data on the usage of DAAs in BCLC-B/C patients, discusses the concept of "the point of no return" in the setting of DAAs, and proposes tools for deciding the best option for each patient profile. If liver function improvement overlaps with symptomatic HCC progression, the benefits of DAAs could be minimised, worsened, or fully counterbalanced. If the BCLC stage is defined using only liver dysfunction, the decision to prioritise DAA treatment should be based on the option (or lack thereof) of liver transplantation and/or the HCC stage. We propose applying a shared decision-making approach, informing each patient of all the potential risks and benefits of the proposed medical intervention.
Copyright © 2021 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  BCLC-B; BCLC-C; BCLC-D; DAA; HCC; liver function; recurrence

Mesh:

Substances:

Year:  2021        PMID: 33582128     DOI: 10.1016/j.jhep.2021.01.046

Source DB:  PubMed          Journal:  J Hepatol        ISSN: 0168-8278            Impact factor:   25.083


  5 in total

1.  First-Line Immune Checkpoint Inhibitor-Based Sequential Therapies for Advanced Hepatocellular Carcinoma: Rationale for Future Trials.

Authors:  Giuseppe Cabibbo; Maria Reig; Ciro Celsa; Ferran Torres; Salvatore Battaglia; Marco Enea; Giacomo Emanuele Maria Rizzo; Salvatore Petta; Vincenza Calvaruso; Vito Di Marco; Antonio Craxì; Amit G Singal; Jordi Bruix; Calogero Cammà
Journal:  Liver Cancer       Date:  2021-11-23       Impact factor: 11.740

Review 2.  Hepatitis B Virus-Associated Hepatocellular Carcinoma.

Authors:  Giacomo Emanuele Maria Rizzo; Giuseppe Cabibbo; Antonio Craxì
Journal:  Viruses       Date:  2022-05-07       Impact factor: 5.818

3.  RBM23 Drives Hepatocellular Carcinoma by Activating NF-κB Signaling Pathway.

Authors:  Hexu Han; Ting Lin; Ziyi Fang; Guoxiong Zhou
Journal:  Biomed Res Int       Date:  2021-03-17       Impact factor: 3.411

4.  Mir-454-3p induced WTX deficiency promotes hepatocellular carcinoma progressions through regulating TGF-β signaling pathway.

Authors:  Hui Liu; Juan Zheng; Shengqian Yang; Qibei Zong; Zhiwen Wang; Xinghua Liao
Journal:  J Cancer       Date:  2022-03-21       Impact factor: 4.207

5.  Elevated Liver Enzymes in a Patient With Hepatocellular Carcinoma on Immune Checkpoint Inhibitor Therapy: A Diagnostic and Therapeutic Challenge.

Authors:  Daniyal Abbas; Lee-Ching Zhu; Andrew M Moon
Journal:  ACG Case Rep J       Date:  2022-07-20
  5 in total

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