Coexistence of oral mucous membrane pemphigoid and lichenoid drug reaction: a case of toripalimab-triggered and pembrolizumab-aggravated oral adverse events.

Oral Surg Oral Med Oral Pathol Oral Radiol

State Key Laboratory of Oral Diseases, National Center of Stomatology, National Clinical Research Center for Oral Diseases, Chinese Academy of Medical Sciences Research Unit of Oral Carcinogenesis and Management, West China Hospital of Stomatology, Sichuan University, Chengdu, Sichuan, China. Electronic address:

Published: September 2021

AI Article Synopsis

  • Toripalimab and pembrolizumab are monoclonal antibodies used to treat various cancers but can lead to mucocutaneous adverse effects, including oral mucous membrane pemphigoid and lichenoid reactions.
  • This report presents a unique case where the patient's condition worsened after switching from toripalimab to pembrolizumab.
  • Although stopping the medications typically resolves these side effects, research indicates a link between skin reactions and better cancer treatment outcomes, highlighting the need for further studies to balance effective cancer control with minimizing adverse events.

Article Abstract

Toripalimab and pembrolizumab belong to anti-programmed death receptor-1 monoclonal antibodies for the treatment of various cancers. Anti-programmed death receptor-1 therapy can cause mucocutaneous adverse events. Here, we report the first case, to our knowledge, of oral mucous membrane pemphigoid and lichenoid reaction triggered by toripalimab and aggravated by switching to pembrolizumab. Mucous membrane pemphigoid was a definite diagnosis, whereas lichenoid reaction was a clinical diagnosis without pathologic evidence. Although discontinuation of the culprit drugs achieved clinical resolution in most reported cases, multiple studies demonstrated statistically significant associations between the development of dermatologic adverse events and superior clinical outcomes. Thus, more studies are needed to find satisfactory measures in terms of both cancer control and avoidance of severe adverse events.

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http://dx.doi.org/10.1016/j.oooo.2021.05.012DOI Listing

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