Small cell neuroendocrine carcinoma of the cervix: From molecular basis to therapeutic advances

Biomed J. 2023 Oct;46(5):100633. doi: 10.1016/j.bj.2023.100633. Epub 2023 Jul 17.

Abstract

Small cell neuroendocrine carcinoma of the cervix (SCNECC) is an uncommon but aggressive uterine malignancy, the cause of which is generally associated with human papillomavirus (HPV) infection. A lack of clinical trials and evidence-based treatment guidelines poses therapeutic challenges to this rare tumor. At present, published data remain limited to case series and case reports. While clinical management has traditionally followed those of small cell neuroendocrine (SCNE) lung cancer relying on surgery, chemoradiation, and systemic chemotherapy, the prognosis remains dismal. Immune checkpoint inhibitors (ICIs), such as monoclonal antibodies that target programmed death-1 (PD-1) or programmed death-ligand 1 (PD-L1), atezolizumab and durvalumab have proven effective in extensive-stage SCNE lung cancer. Moreover, pembrolizumab has also proven beneficial effects when added onto chemotherapy in metastatic and recurrent HPV-associated non-SCNE cervical cancer. It holds promise to use ICIs in combination with chemoradiation to improve the clinical outcomes of patients with SCNECC. Future advances in our understanding of SCNECC biology - associated with the study of its genomic and molecular aberrations as well as knowledge from SCNE of lung and other extrapulmonary sites- would be helpful in discovering new molecular targets for drug development. Collaborative efforts and establishment of a SCNECC-specific biobank will be essential to achieve this goal.

Keywords: Immune checkpoint inhibitors; Molecular targets; Small cell neuroendocrine carcinoma; Uterine cervix.

Publication types

  • Review

MeSH terms

  • B7-H1 Antigen / therapeutic use
  • Carcinoma, Neuroendocrine* / drug therapy
  • Carcinoma, Neuroendocrine* / genetics
  • Cervix Uteri / pathology
  • Female
  • Humans
  • Lung Neoplasms* / pathology
  • Papillomavirus Infections*
  • Uterine Cervical Neoplasms* / drug therapy

Substances

  • B7-H1 Antigen