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Trial watch: Immune checkpoint blockers for cancer therapy

  • Claire Vanpouille-Box
  • , Claire Lhuillier
  • , Lucillia Bezu
  • , Fernando Aranda
  • , Takahiro Yamazaki
  • , Oliver Kepp
  • , Jitka Fucikova
  • , Radek Spisek
  • , Sandra Demaria
  • , Silvia C. Formenti
  • , Laurence Zitvogel
  • , Guido Kroemer
  • , Lorenzo Galluzzi
  • Cornell University
  • Université Paris Cité
  • Sorbonne Université
  • Centre de Recherche des Cordeliers
  • Institut national de la santé et de la recherche médicale
  • Université Paris-Sud
  • August Pi i Sunyer Biomedical Research Institute
  • Sotio
  • Charles University
  • Gustave Roussy Cancer Campus
  • Center of Clinical Investigations in Biotherapies of Cancer (CICBT)
  • Université Paris-Saclay
  • Karolinska Institutet
  • Assistance publique – Hôpitaux de Paris

Research output: Contribution to journalReview articlepeer-review

67 Scopus citations

Abstract

Immune checkpoint blockers (ICBs) are literally revolutionizing the clinical management of an ever more diversified panel of oncological indications. Although considerable attention persists around the inhibition of cytotoxic T lymphocyte-associated protein 4 (CTLA4) and programmed cell death 1 (PDCD1, best known as PD-1) signaling, several other co-inhibitory T-cell receptors are being evaluated as potential targets for the development of novel ICBs. Moreover, substantial efforts are being devoted to the identification of biomarkers that reliably predict the likelihood of each patient to obtain clinical benefits from ICBs in the absence of severe toxicity. Tailoring the delivery of specific ICBs or combinations thereof to selected patient populations in the context of precision medicine programs constitutes indeed a major objective of the future of ICB-based immunotherapy. Here, we discuss recent preclinical and clinical advances on the development of ICBs for oncological indications.

Original languageEnglish
Article numbere1373237
JournalOncoimmunology
Volume6
Issue number11
DOIs
StatePublished - Nov 2 2017
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Atezolizumab
  • avelumab
  • durvalumab
  • ipilimumab
  • nivolumab
  • pembrolizumab

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