Immunotherapy in Head and Neck Cancer: Where Do We Stand?

Curr Oncol Rep. 2023 Aug;25(8):897-912. doi: 10.1007/s11912-023-01425-1. Epub 2023 May 22.

Abstract

Purposeof review: Head and neck cancer (HNC) comprises a group of malignancies, amongst which squamous cell carcinoma accounts for more than 90% of the cases. HNC has been related to tobacco use, alcohol consumption, human papillomavirus, Epstein-Barr virus, air pollution, and previous local radiotherapy. HNC has been associated with substantial morbidity and mortality. This review aims to summarize the recent findings regarding immunotherapy in HNC.

Recent findings: The recent introduction of immunotherapy, with the use of programmed death 1 (PD-1) inhibitors pembrolizumab and nivolumab, which have been FDA approved for the treatment of metastatic or recurrent head and neck squamous cell carcinoma, has changed the field in metastatic or recurrent disease. There are many ongoing trials regarding the use of novel immunotherapeutic agents, such as durvalumab, atezolizumab, avelumab, tremelimumab, and monalizumab. In this review, we focus on the therapeutic potential of novel immunotherapy treatment modalities, such as combinations of newer immune-checkpoint inhibitors; the use of tumor vaccines such as human papillomavirus-targeted vaccines; the potential use of oncolytic viruses; as well as the latest advances regarding adoptive cellular immunotherapy. As novel treatment options are still emerging, a more personalized approach to metastatic or recurrent HNC therapy should be followed. Moreover, the role of the microbiome in immunotherapy, the limitations of immunotherapy, and the various diagnostic, prognostic, and predictive biomarkers based on genetics and the tumor microenvironment are synopsized.

Keywords: Head and neck cancer; Immune-checkpoint inhibitors; Immunotherapy; Oncolytic viruses; Programmed death 1; Tumor microenvironment; Tumor vaccines.

Publication types

  • Review

MeSH terms

  • Epstein-Barr Virus Infections*
  • Head and Neck Neoplasms* / therapy
  • Herpesvirus 4, Human
  • Humans
  • Immunotherapy
  • Neoplasm Recurrence, Local / therapy
  • Tumor Microenvironment