Angiogenesis and immune checkpoint inhibitors as therapies for hepatocellular carcinoma: current knowledge and future research directions.


Journal

Journal for immunotherapy of cancer
ISSN: 2051-1426
Titre abrégé: J Immunother Cancer
Pays: England
ID NLM: 101620585

Informations de publication

Date de publication:
29 11 2019
Historique:
received: 17 06 2019
accepted: 13 11 2019
entrez: 1 12 2019
pubmed: 1 12 2019
medline: 22 7 2020
Statut: epublish

Résumé

Hepatocellular carcinoma (HCC) is the second deadliest cancer worldwide, due to its high incidence and poor prognosis. Frequent initial presentation at advanced stages along with impaired liver function limit the use of a broad therapeutic arsenal in patients with HCC. Although main HCC oncogenic drivers have been deciphered in recent years (TERT, TP53, CTNNB1 mutations, miR122 and CDKN2A silencing), therapeutic applications derived from this molecular knowledge are still limited. Given its high vascularization and immunogenicity, antiangiogenics and immune checkpoint inhibitors (ICI), respectively, are two therapeutic approaches that have shown efficacy in HCC. Depending on HCC immune profile, combinations of these therapies aim to modify the protumoral/antitumoral immune balance, and to reactivate and favor the intratumoral trafficking of cytotoxic T cells. Combination therapies involving antiangiogenics and ICI may be synergistic, because vascular endothelial growth factor A inhibition increases intratumoral infiltration and survival of cytotoxic T lymphocytes and decreases regulatory T lymphocyte recruitment, resulting in a more favorable immune microenvironment for ICI antitumoral activity. First results from clinical trials evaluating combinations of these therapies are encouraging with response rates never observed before in patients with HCC. A better understanding of the balance and interactions between protumoral and antitumoral immune cells will help to ensure the success of future therapeutic trials. Here, we present an overview of the current state of clinical development of antitumoral therapies in HCC and the biological rationale for their use. Moreover, translational studies on tumor tissue and blood, prior to and during treatment, will help to identify biomarkers and immune signatures with predictive value for both clinical outcome and response to combination therapies.

Identifiants

pubmed: 31783782
doi: 10.1186/s40425-019-0824-5
pii: 10.1186/s40425-019-0824-5
pmc: PMC6884868
doi:

Substances chimiques

Angiogenesis Inhibitors 0
Antineoplastic Agents, Immunological 0
Biomarkers, Tumor 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

333

Subventions

Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States

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Auteurs

Marc Hilmi (M)

Department of Medical Oncology, Curie Institute, University of Versailles Saint-Quentin, Paris, France.

Cindy Neuzillet (C)

Department of Medical Oncology, Curie Institute, University of Versailles Saint-Quentin, Paris, France.

Julien Calderaro (J)

Department of Pathology, Henri Mondor Hospital, Créteil, France.
IMRB-INSERM U955 Team 18, Créteil, France.
Université Paris-Est-Créteil, Créteil, France.

Fouad Lafdil (F)

IMRB-INSERM U955 Team 18, Créteil, France.
Université Paris-Est-Créteil, Créteil, France.
Institut Universitaire de France, Paris, France.

Jean-Michel Pawlotsky (JM)

IMRB-INSERM U955 Team 18, Créteil, France.
Université Paris-Est-Créteil, Créteil, France.
National Reference Center for Viral Hepatitis B, C and D, Department of Virology, Henri Mondor Hospital, Créteil, France.

Benoit Rousseau (B)

IMRB-INSERM U955 Team 18, Créteil, France. ben.rousseau@gmail.com.
Department of Medicine, Division of Solid Tumor Oncology, Memorial Sloan Kettering Cancer Center, New York, NY, USA. ben.rousseau@gmail.com.

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