Are we ready for deintensification in human papillomavirus-positive oropharyngeal carcinomas?

Curr Opin Otolaryngol Head Neck Surg. 2023 Apr 1;31(2):118-128. doi: 10.1097/MOO.0000000000000871. Epub 2023 Jan 31.

Abstract

Purpose of review: Excellent outcomes following contemporary treatment of human papillomavirus (HPV)-positive oropharyngeal carcinoma (HPV+ OPC) have prompted the exploration of deintensification approaches to minimize treatment-related toxicities. This review describes the landscape of deintensification to date (up to November 2022).

Recent findings: Although several deintensification trials have been published, none are practice changing. Three phase III randomized-controlled trials studying cetuximab and radiation therapy vs. standard chemoradiotherapy all showed inferior outcomes. Although some phase II trials reported favourable outcomes, they are often single-arm trials without an adequate control arm, thereby limiting the ability to modify practice.

Summary: Substantial effort has been expended to explore deintensification options for selected HPV+ OPC patients aiming to avoid unnecessary toxicity. Strategies have included replacing cisplatin with cetuximab, reduced chemotherapy or radiotherapy intensity, reduction of radiotherapy volumes and risk stratification after trans-oral surgery or following induction chemotherapy. Challenges remain in the current deintensification landscape, including identifying the most suitable candidates along with a choice of most appropriate deintensification strategies. Promising selection criteria included either static baseline features or kinetic characteristics of clinical-biological parameters. Practice-changing trials remain elusive, and the search continues to attempt optimization of the therapeutic ratio for these patients.

Publication types

  • Review

MeSH terms

  • Carcinoma*
  • Cetuximab
  • Chemoradiotherapy
  • Human Papillomavirus Viruses
  • Humans
  • Oropharyngeal Neoplasms* / pathology
  • Papillomavirus Infections*

Substances

  • Cetuximab