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

Authors :
Jochen Utikal
Jessica C. Hassel
Daniela Göppner
Martin Leverkus
Maria I. Schmidgen
Reinhard Dummer
Thomas Eigentler
Carola Berking
Anja Gesierich
Lisa Zimmer
Ursula Dietrich
Andrea Forschner
Angela M. Krackhardt
Friedegund Meier
Gerold Schuler
Carsten Weishaupt
Ioannis Thomas
Simone M. Goldinger
Ralf Gutzmer
Claus Garbe
Selma Ugurel
Dirk Schadendorf
Carmen Loquai
Lars Hofmann
Lucie Heinzerling
Renate Ursula Wahl
Julia K. Tietze
Michael C. Kirchberger
Source :
European journal of cancer (Oxford, England : 1990). 60
Publication Year :
2016

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

ISSN :
18790852
Volume :
60
Database :
OpenAIRE
Journal :
European journal of cancer (Oxford, England : 1990)
Accession number :
edsair.doi.dedup.....263bce5158d70c2cbeead10f02368ef9