Clinical characterization of colitis arising from anti-PD-1 based therapy

Colitis is a frequent, clinically-significant immune-related adverse event caused by anti-programmed death-1 (PD-1). The clinical features, timing, and management of colitis with anti-PD-1-based regimens are not well-characterized. Patients with advanced melanoma that received either anti-PD-1 monot...

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Veröffentlicht in:Oncoimmunology 2019-01, Vol.8 (1), p.e1524695-e1524695
Hauptverfasser: Wang, Daniel Y, Mooradian, Meghan J, Kim, DaeWon, Shah, Neil J, Fenton, Sarah E, Conry, Robert M, Mehta, Rutika, Silk, Ann W., Zhou, Alice, Compton, Margaret L, Al-Rohil, Rami N, Lee, Sunyoung, Voorhees, Amber L, Ha, Lisa, McKee, Svetlana, Norrell, Jacqueline T, Mehnert, Janice, Puzanov, Igor, Sosman, Jeffrey A, Chandra, Sunandana, Gibney, Geoffrey T, Rapisuwon, Suthee, Eroglu, Zeynep, Sullivan, Ryan, Johnson, Douglas B
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Sprache:eng
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Zusammenfassung:Colitis is a frequent, clinically-significant immune-related adverse event caused by anti-programmed death-1 (PD-1). The clinical features, timing, and management of colitis with anti-PD-1-based regimens are not well-characterized. Patients with advanced melanoma that received either anti-PD-1 monotherapy ("monotherapy") or combined with ipilimumab ("combination therapy") were screened from 8 academic medical centers, to identify those with clinically-relevant colitis (colitis requiring systemic steroids). Of 1261 patients who received anti-PD-1-based therapy, 109 experienced colitis. The incidence was 3.2% (30/937) and 24.4% (79/324) in the monotherapy and combination therapy cohorts, respectively. Patients with colitis from combination therapy had significantly earlier symptom onset (7.2 weeks vs 25.4 weeks, p 
ISSN:2162-4011
2162-402X
2162-402X
DOI:10.1080/2162402X.2018.1524695