[PD-L1 expression and PD-1/PD-L1 inhibitors in breast cancer]

Bull Cancer. 2018 Mar;105(3):263-274. doi: 10.1016/j.bulcan.2017.11.012. Epub 2018 Feb 16.
[Article in French]

Abstract

The development of immune checkpoints inhibitors represents one of the major recent advances in oncology. Monoclonal antibodies directed against the programmed cell death protein 1 (PD-1) or its ligand (PD-L1) provides durable disease control, particularly in melanoma, lung, kidney, bladder and head and neck cancers. The purpose of this review is to synthesize current data on the expression of PD-L1 in breast cancer and on the preliminary clinical results of PD-1/PD-L1 inhibitors in breast cancer patients. In breast cancer, PD-L1 expression is heterogeneous and is generally associated with the presence of tumor-infiltrating lymphocytes as well as the presence of poor-prognosis factors, such as young age, high grade, ER-negativity, PR-negativity, and HER-2 overexpression, high proliferative index, and aggressive molecular subtypes (triple negative, basal-like, HER-2-overexpressing). Its prognostic value remains controversial when assessed with immunohistochemistry, whereas it seems favorable in triple-negative cancers when assessed at the mRNA level. Early clinical trials with PD-1/PD-L1 inhibitors in breast cancer have shown efficacy in terms of tumor response and/or disease control in refractory metastatic breast cancers, notably in the triple-negative subtype. Many trials are currently underway, both in the metastatic and neo-adjuvant setting. A crucial issue is identification of biomarkers predictive of response to PD-1/PD-L1 inhibitors.

Keywords: Breast cancer; Cancer du sein; Clinical trials; Essais cliniques; Expression; Immunotherapy; Immunothérapie; PD-1; PD-L1.

Publication types

  • Review

MeSH terms

  • Antibodies, Monoclonal / therapeutic use
  • B7-H1 Antigen / antagonists & inhibitors*
  • Breast Neoplasms / metabolism*
  • Breast Neoplasms / therapy*
  • Clinical Trials as Topic
  • Female
  • Humans
  • Lymphocytes, Tumor-Infiltrating
  • Neoplasm Proteins / antagonists & inhibitors
  • Neoplasm Proteins / metabolism
  • Prognosis
  • Programmed Cell Death 1 Receptor / antagonists & inhibitors*
  • Programmed Cell Death 1 Receptor / metabolism
  • Risk Factors
  • Triple Negative Breast Neoplasms / metabolism
  • Triple Negative Breast Neoplasms / therapy

Substances

  • Antibodies, Monoclonal
  • B7-H1 Antigen
  • CD274 protein, human
  • Neoplasm Proteins
  • Programmed Cell Death 1 Receptor