Research Paper Volume 12, Issue 11 pp 10663—10675

Association between immune-related adverse events and efficacy of PD-1 inhibitors in Chinese patients with advanced melanoma

Jing-Jing Zhao1,2, *, , Xi-Zhi Wen1,2, *, , Ya Ding1,2, , Dan-Dan Li1,2, , Bao-Yan Zhu1,2, , Jing-Jing Li1,2, , De-Sheng Weng1,2, , Xing Zhang1,2, , Xiao-Shi Zhang1,2, ,

  • 1 Sun Yat-Sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangzhou, China
  • 2 Department of Biotherapy, Sun Yat-Sen University Cancer Center, Guangzhou, China
* Equal contribution

Received: November 17, 2019       Accepted: April 27, 2020       Published: June 8, 2020      

https://doi.org/10.18632/aging.103285
How to Cite

Copyright © 2020 Zhao et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Abstract

Programmed cell death 1 (PD-1) checkpoint inhibitor therapy leads to immune-related adverse events (irAEs). We sought to evaluate whether the development of irAEs correlates with the treatment response in Chinese patients with advanced melanoma. In this study, we conducted a retrospective study of advanced melanoma patients who received PD-1 inhibitor therapy in China between August 2014 and March 2018. A total of 93 patients treated with PD-1 inhibitors including pembrolizumab and nivolumab were enrolled. The most frequent irAEs were pruritus, rash, vitiligo, and fatigue. The median time to onset of irAEs was 6.1 weeks. The overall response rate (ORR) and disease control rate (DCR) were higher in patients with irAEs than those without irAEs (P = 0.004 and P = 0.003, respectively), and better in patients who experienced three or more irAEs than those with none (P <0.001 and P <0.001, respectively). The ORR and DCR were significantly better in patients with grade 1 to 2 irAEs when compared with those with none (P = 0.002 and P = 0.003, respectively). In addition, the median progression-free survival and overall survival were longer in patients with irAEs than in those without irAEs (P = 0.007 and P = 0.002, respectively). In conclusion, our data demonstrated that irAEs were associated with a better clinical outcome after treatment with PD-1 inhibitor therapy in Chinese patients with advanced melanoma.

Abbreviations

PD-1: programmed cell death 1; irAEs: immune-related adverse events; ORR: overall response rate; DCR: disease control rate; PFS: progression-free survival; OS: overall survival; ICIs: immune checkpoint inhibitors; NSCLC: non–small cell lung cancer; CSD: chronic sun-derived; ORR: the objective response rate; DCR: disease control rate; PFS: progression-free survival; OS: overall survival; NR: Not reached; CR: complete remission; PR: partial remission; SD: stable disease; PD: progressive disease.