Challenges of combination therapy with immune checkpoint inhibitors for hepatocellular carcinoma.
Angiogenesis Inhibitors
/ therapeutic use
Antibodies, Monoclonal, Humanized
/ therapeutic use
Antineoplastic Agents, Immunological
/ therapeutic use
B7-H1 Antigen
/ antagonists & inhibitors
Biomarkers, Tumor
/ blood
CTLA-4 Antigen
/ antagonists & inhibitors
Carcinoma, Hepatocellular
/ blood
Combined Modality Therapy
/ methods
Humans
Immune Checkpoint Inhibitors
/ pharmacology
Immunotherapy
/ methods
Liver Neoplasms
/ blood
Programmed Cell Death 1 Receptor
/ antagonists & inhibitors
Progression-Free Survival
T-Lymphocytes
/ immunology
Biomarker
Combination
Hepatocellular carcinoma
Immune checkpoint inhibitor
Journal
Journal of hepatology
ISSN: 1600-0641
Titre abrégé: J Hepatol
Pays: Netherlands
ID NLM: 8503886
Informations de publication
Date de publication:
02 2020
02 2020
Historique:
received:
04
07
2019
revised:
09
09
2019
accepted:
28
09
2019
entrez:
20
1
2020
pubmed:
20
1
2020
medline:
8
7
2021
Statut:
ppublish
Résumé
Immune checkpoint inhibitor (ICI) therapy targeting anti-programmed cell death-1 (anti-PD-1) or its ligand (anti-PD-L1) is the backbone of numerous combination regimens aimed at improving the objective response and survival of patients with hepatocellular carcinoma (HCC). Clinical trials of immuno-oncology regimens in other cancer types have shed light on issues of study design, including how to choose candidate regimens based on early-phase trial results, statistical considerations in trials with multiple primary endpoints, and the importance of predictive biomarkers. In this review, the updated data from early-phase trials of combination immunotherapy for HCC are summarised. Since the most extensively tested combination regimens for advanced HCC comprise anti-PD-1/anti-PD-L1 agents plus antiangiogenic agents, the relative benefit and antitumor mechanism of antiangiogenic multikinase inhibitors versus specific VEGF/VEGFR inhibitors are discussed. Other critical issues in the development of combination immunotherapy, including optimal management of immune-related adverse events and the value of ICI therapy in combination with locoregional treatment for HCC, are also explored.
Identifiants
pubmed: 31954494
pii: S0168-8278(19)30591-4
doi: 10.1016/j.jhep.2019.09.025
pii:
doi:
Substances chimiques
Angiogenesis Inhibitors
0
Antibodies, Monoclonal, Humanized
0
Antineoplastic Agents, Immunological
0
B7-H1 Antigen
0
Biomarkers, Tumor
0
CD274 protein, human
0
CTLA-4 Antigen
0
CTLA4 protein, human
0
Immune Checkpoint Inhibitors
0
PDCD1 protein, human
0
Programmed Cell Death 1 Receptor
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
307-319Informations de copyright
Copyright © 2019 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.