The immune microenvironment and HPV in anal cancer: Rationale to complement chemoradiation with immunotherapy

Biochim Biophys Acta Rev Cancer. 2017 Aug;1868(1):221-230. doi: 10.1016/j.bbcan.2017.05.001. Epub 2017 May 10.

Abstract

Anal squamous cell carcinomas (ASCC) are increasing in frequency across the developed world, and 70-90% of all cases originate from infection with human papilloma viruses (HPV). Primary chemoradiotherapy (CRT) is the standard treatment for ASCC, but local and/or distant failure still occurs in up to 30% of patients. HPV-associated ASCC and tumors with a higher density of tumor infiltrating lymphocytes (TIL) carry a better prognosis. Furthermore, HPV can render tumors more immunogenic, whereas it correlates with elevated TIL densities. This comprehensive review highlights the progress made in understanding the immune microenvironment of anal intraepithelial neoplasias and ASCC in the context of HPV. Here, we discuss the immunomodulatory potential of CRT, the prognostic impact of immune checkpoint markers, and the rationale for including immunotherapies to further improve the clinical outcome in patients with ASCC.

Keywords: Anal cancer; HPV; Immune; Immunotherapy; Microenvironment; Prognostic.

Publication types

  • Review

MeSH terms

  • Anus Neoplasms / immunology*
  • Anus Neoplasms / therapy*
  • Anus Neoplasms / virology
  • Carcinoma, Squamous Cell / immunology
  • Carcinoma, Squamous Cell / therapy
  • Carcinoma, Squamous Cell / virology
  • Chemoradiotherapy / methods
  • Humans
  • Immunotherapy / methods
  • Papillomaviridae / immunology*
  • Papillomavirus Infections / immunology
  • Papillomavirus Infections / virology
  • Prognosis
  • Tumor Microenvironment / immunology*