Literature DB >> 30348532

Immune-related adverse events are linked with improved progression-free survival in patients receiving anti-PD-1/PD-L1 therapy.

Hammad Shafqat1, Theodore Gourdin2, Amy Sion3.   

Abstract

BACKGROUND: Immune-related adverse events (irAEs) are commonly encountered, when using programmed death-1/programmed death-ligand-1 (anti-PD-1/PD-L1) therapy and are often managed with corticosteroids. The effect of irAEs, particularly when steroids are required, on patient survival is not well established.
METHODS: In this retrospective analysis, data for 157 patients with various tumor types treated with anti-PD-1/PD-L1 therapy were obtained. Kaplan-Meier and Cox regression analyses were used to assess the effect of irAEs and corticosteroids on progression-free survival (PFS).
RESULTS: A total of 45 irAEs were recorded for 157 patients. Twenty-one patients received systemic corticosteroids. Patients who developed irAEs, as well as those who received systemic corticosteroids, had improved PFS by Kaplan-Meier estimate. Multivariate Cox regression showed that irAEs were associated with improved PFS (hazard ratio of 0.33, P <0.001) which persisted even with use of systemic corticosteroids (hazard ratio of 0.38, P = 0.03).
CONCLUSIONS: irAEs are associated with improved PFS in patients receiving anti-PD-1/PD-L1 therapy. This association does not appear to be altered by the use of systemic corticosteroids.
Copyright © 2018 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Immune-mediated adverse events; checkpoint inhibitors; corticosteroids; immunotherapy

Mesh:

Substances:

Year:  2018        PMID: 30348532     DOI: 10.1053/j.seminoncol.2018.07.003

Source DB:  PubMed          Journal:  Semin Oncol        ISSN: 0093-7754            Impact factor:   4.929


  15 in total

1.  Immune-related adverse events: promising predictors for efficacy of immune checkpoint inhibitors.

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Review 9.  Current Clinical Progress of PD-1/PD-L1 Immunotherapy and Potential Combination Treatment in Non-Small Cell Lung Cancer.

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