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

被引:54
|
作者
Shafqat, Hammad [1 ]
Gourdin, Theodore [1 ]
Sion, Amy [2 ]
机构
[1] Med Univ South Carolina, Div Hematol & Oncol, 39 Sabin St,MSC 635, Charleston, SC 29425 USA
[2] Med Univ South Carolina, Dept Pharm, 150 Ashley Ave, Charleston, SC 29425 USA
基金
美国国家卫生研究院;
关键词
Immune-mediated adverse events; corticosteroids; checkpoint inhibitors; immunotherapy; MELANOMA; IPILIMUMAB; NIVOLUMAB; ASSOCIATION; VITILIGO; BLOCKADE; PEMBROLIZUMAB; MANAGEMENT; TOXICITIES;
D O I
10.1053/j.seminoncol.2018.07.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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 antiPD-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. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:156 / 163
页数:8
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