[Immune checkpoints inhibitors: Recent data from ASCO's meeting 2017 and perspectives]

Bull Cancer. 2018 Jul-Aug;105(7-8):686-695. doi: 10.1016/j.bulcan.2018.04.011. Epub 2018 Jun 20.
[Article in French]

Abstract

Immune checkpoint inhibitors anti-PD-1, anti-PD-L1 and anti-CTLA-4 have been in development in several indications and have changed the face of cancer patients' management. Cancer immunotherapy was central in ASCO's meeting 2017. The identification of patients who could benefit most from immune checkpoint inhibitors is essential. The predictive value of PD-L1 status remains insufficient to select patients who could respond to immunotherapy. An extended search for new biomarkers predictive of response (INF-γ, mutational load) is ongoing, in order to better select responders. Immune checkpoint inhibitors have mainly been developed as monotherapy. However, the low response rate, between 10 and 30%, and the occurrence of resistance, contributes to the increment of new therapeutic strategies. This review summarizes the results of combination trials of two immune checkpoint inhibitors, combination of immunotherapy with conventional chemotherapy, radiotherapy or targeted therapies active on the oncogenic addiction pathway.

Keywords: Biomarkers; Biomarqueurs; Combinaisons; Combinations; Immune checkpoint inhibitors; Immunotherapy; Immunothérapie; Inhibiteurs de checkpoints immunitaires; PD-1/PD-L1.

Publication types

  • Review

MeSH terms

  • Antineoplastic Agents / therapeutic use*
  • B7-H1 Antigen / antagonists & inhibitors*
  • Biomarkers, Tumor
  • CTLA-4 Antigen / antagonists & inhibitors*
  • Combined Modality Therapy / methods
  • Congresses as Topic*
  • Humans
  • Immunotherapy / methods*
  • Medical Oncology
  • Molecular Targeted Therapy
  • Programmed Cell Death 1 Receptor / antagonists & inhibitors*
  • Radiotherapy
  • Societies, Medical

Substances

  • Antineoplastic Agents
  • B7-H1 Antigen
  • Biomarkers, Tumor
  • CD274 protein, human
  • CTLA-4 Antigen
  • PDCD1 protein, human
  • Programmed Cell Death 1 Receptor