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. 2021 Oct;75(4):960-974.
doi: 10.1016/j.jhep.2021.07.004. Epub 2021 Jul 10.

Systemic treatment of hepatocellular carcinoma: An EASL position paper

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Systemic treatment of hepatocellular carcinoma: An EASL position paper

Jordi Bruix et al. J Hepatol. 2021 Oct.

Abstract

The last 5 years have witnessed relevant advances in the systemic treatment of hepatocellular carcinoma. New data have emerged since the development of the EASL Clinical Practice Guidelines on the management of hepatocellular carcinoma in 2018. Drugs licensed in some countries now include 4 oral multi-tyrosine kinase inhibitors (sorafenib, lenvatinib, regorafenib and cabozantinib), 1 anti-angiogenic antibody (ramucirumab) and 4 immune checkpoint inhibitors, alone or in combination (atezolizumab in combination with bevacizumab, ipilimumab in combination with nivolumab, nivolumab and pembrolizumab in monotherapy). Prolonged survival in excess of 2 years can be expected in most patients with sensitive tumours and well-preserved liver function that renders them fit for sequential therapies. With different choices available in any given setting, the robustness of the evidence of efficacy and a correct matching of the safety profile of a given agent with patient characteristics and preferences are key in making sound therapeutic decisions. The recommendations in this document amend the previous EASL Clinical Practice Guidelines and aim to help clinicians provide the best possible care for patients today. In view of several ongoing and promising trials, further advances in systemic therapy of hepatocellular carcinoma are foreseen in the near future and these recommendations will have to be updated regularly.

Keywords: hepatoma; immune-checkpoint inhibitors; immunotherapy; liver cancer; liver toxicity; tyrosine kinase inhibitors.

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Conflict of interest statement

Conflict of interest JB received received consulting fees from AbbVie, Adaptimmune, Arqule, AstraZeneca, Medimmune, Basilea, Bayer, Bio-Alliance, BMS, BTG, Eisai, Gilead, Incyte, Ipsen, Kowa, Lilly, MSD, Nerviano, Novartis, Polaris, Quirem, Roche, Sirtex, Sanofi, Terumo; institutional research grants from Bayer, BTG; educational grants from Bayer, BTG; and speaker fees from Bayer, BTG, Ipsen, Roche, Eisai, Terumo, Sirtex. SC Stephen L. Chan has acted as an advisor to AstraZeneca, Eisai, MSD and Novartis; received research grants from Bayer, Ipsen, MSD and SIRTEX; and received lecture fees from AstraZeneca,Bayer, Eisai, Roche and MSD. PRG received consulting and/or lecturing fees from Bayer, BMS, AstraZeneca, Sirtex, MSD, Eisai, Ipsen, Roche, Adaptimmune, Lilly. LR received consulting fees from Amgen, ArQule, AstraZeneca, Basilea, Bayer, BMS, Celgene, Eisai, Exelixis, Genenta, Hengrui, Incyte, Ipsen, IQVIA, Lilly, MSD, Nerviano Medical Sciences, Roche, Sanofi, Zymeworks; lecture fees from AbbVie, Amgen, Bayer, Eisai, Gilead, Incyte, Ipsen, Lilly, Merck Serono, Roche, Sanofi; travel expenses from Ipsen; and institutional research funding from Agios, ARMO BioSciences, AstraZeneca, BeiGene, Eisai, Exelixis, Fibrogen, Incyte, Ipsen, Lilly, MSD, Nerviano Medical Sciences, Roche, Zymeworks. BS received consulting fees from Adaptimmune, AstraZeneca, Bayer, BMS, BTG, Eisai, Exelixis, Eli-Lilly, IPSEN, Merck, Onxeo, Roche, Sirtex; lecture fees from AstraZeneca, Bayer, BMS, Eisai, Eli-Lilly, Incyte, IPSEN, Roche, Sirtex; institutional research grants from BMS and Sirtex. Please refer to the accompanying ICMJE disclosure forms for further details.

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