[Immunotherapy in oncogynaecology]

Bull Cancer. 2023 Apr;110(4):395-401. doi: 10.1016/j.bulcan.2023.01.004. Epub 2023 Feb 8.
[Article in French]

Abstract

Immune checkpoint inhibitors have deeply changed treatment paradigm of many tumor types, notably by providing long-term remissions, even in the metastatic setting. These immunotherapies aim to restore T-cells activity against tumour cells, in particular via the inhibition of PD1/PD-L1 interaction. As for lung or renal carcinomas, and melanomas, the management of endometrial and uterine cervical cancers has been disrupted by PD1/PD-L1 inhibitors efficacy. In locally advanced or metastatic cervical carcinomas, the combination of platinum-based chemotherapy with pembrolizumab demonstrated improved overall and progression-free survival in all subgroups of patients, and became the new standard of care. Regarding endometrial cancers, while single-agent immunotherapies have shown very limited activity in an unselected population, dostarlimab and pembrolizumab have been associated with remarkable antitumor activity in case of microsatellite instability (dMMR/MSI), detected in around 30% of patients. Finally, in endometrial cancer that has progressed after first-line chemotherapy, the association of pembrolizumab with an oral antiangiogenic kinase inhibitor (lenvatinib) has demonstrated its superiority over second-line chemotherapy regimens, regardless molecular subgroups, and has become the new standard of care in this indication.

Keywords: Cancer de l’endomètre; Cancer de l’ovaire; Cancer du col utérin; Immunotherapy; Immunothérapie; Ovarian neoplasms; Uterine cervical neoplasms; Uterine neoplasms.

Publication types

  • English Abstract
  • Review

MeSH terms

  • Antineoplastic Agents* / therapeutic use
  • Brain Neoplasms* / drug therapy
  • Endometrial Neoplasms* / drug therapy
  • Female
  • Humans
  • Immune Checkpoint Inhibitors / therapeutic use
  • Immunotherapy
  • Melanoma* / drug therapy
  • Microsatellite Instability

Substances

  • Antineoplastic Agents
  • Immune Checkpoint Inhibitors