Cutaneous, gastrointestinal, hepatic, endocrine, and renal side-effects of anti-PD-1 therapy

Hofmann L., Forschner A., Loquai C., Goldinger S., Zimmer L., Ugurel S., Schmidgen M., Gutzmer R., Utikal J., Göppner D., Hassel J., Meier F., Tietze J., Thomas I., Weishaupt C., Leverkus M., Wahl R., Dietrich U., Garbe C., Kirchberger M., Eigentler T., Berking C., Gesierich A., Krackhardt A., Schadendorf D., Schuler G., Dummer R., Heinzerling L.

Research article (journal) | Peer reviewed

Abstract

Background Anti-programmed cell death receptor-1 (PD-1) antibodies represent an effective treatment option for metastatic melanoma as well as for other cancer entities. They act via blockade of the PD-1 receptor, an inhibitor of the T-cell effector mechanisms that limit immune responses against tumours. As reported for ipilimumab, the anti-PD-1 antibodies pembrolizumab and nivolumab can induce immune-related adverse events (irAEs). These side-effects affect skin, gastrointestinal tract, liver, endocrine system and other organ systems. Since life-threatening and fatal irAEs have been reported, adequate diagnosis and management are essential. Methods and findings In total, 496 patients with metastatic melanoma from 15 skin cancer centers were treated with pembrolizumab or nivolumab; 242 side-effects were described in 138 patients. In 116 of the 138 patients, side-effects affected the skin, gastrointestinal tract, liver, endocrine, and renal system. Rare side-effects included diabetes mellitus, lichen planus, and pancreas insufficiency due to pancreatitis. Conclusion Anti-PD1 antibodies can induce a plethora of irAEs. The knowledge of them will allow prompt diagnosis and improve the management resulting in decreased morbidity.

Details about the publication

JournalEuropean Journal of Cancer (Eur J Cancer)
Volume60
Issuenull
Page range190-199
StatusPublished
Release year2016
Language in which the publication is writtenEnglish
DOI10.1016/j.ejca.2016.02.025
Link to the full texthttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84964345287&origin=inward
KeywordsAdverse event; Anti-PD-1; Checkpoint inhibitors; Immune-related; Nivolumab; Pembrolizumab; Side-effect; Tolerability; Toxicity

Authors from the University of Münster

Weishaupt, Carsten
Clinic for Dermatology