Association Between the Occurrence and Spectrum of Immune-Related Adverse Events and Efficacy of Pembrolizumab in Asian Patients With Advanced Urothelial Cancer: Multicenter Retrospective Analyses and Systematic Literature Review.


Journal

Clinical genitourinary cancer
ISSN: 1938-0682
Titre abrégé: Clin Genitourin Cancer
Pays: United States
ID NLM: 101260955

Informations de publication

Date de publication:
06 2021
Historique:
received: 30 04 2020
revised: 14 06 2020
accepted: 12 07 2020
pubmed: 18 8 2020
medline: 19 8 2021
entrez: 18 8 2020
Statut: ppublish

Résumé

An association between the development of overall or specific immune-related adverse events (irAEs) and outcomes of immune checkpoint inhibitors has recently been suggested. To address this emerging association in patients with urothelial cancer receiving pembrolizumab, we conducted a multicenter retrospective analysis, which is the first and largest in an Asian cohort as well as a systematic literature review. We retrospectively evaluated 97 patients with advanced urothelial cancer treated with pembrolizumab as second- or later-line treatment between January 2018 and March 2019. irAEs were categorized by the involved organs and graded using Common Terminology Criteria for Adverse Events version 5.0. Associations between irAEs and pembrolizumab efficacy, including objective response rate (ORR), progression-free survival (PFS), and overall survival (OS), were evaluated. In our review of the literature, 28 studies, including 9 studies involving patients with urothelial cancer and 19 studies reporting the association between outcomes and spectrum of irAEs, were analyzed. Patients with irAEs had significantly higher ORR (52% vs. 16%, P < .01), longer PFS (11.0 months vs. 3.6 months, P < .01) and OS (median not reached vs. 13.1 months, P = .12) than in patients without irAEs. Endocrine (P = .02), pneumological (P = .06), and other (gastrointestinal, hematological, hepatic) (P = .04) irAEs were associated with increased ORR, whereas skin irAEs were not. Endocrine irAEs (P = .04) was associated with improved OS, whereas pneumological and skin irAEs were not. The association between the occurrence of irAEs and clinical efficacy of immune checkpoint inhibitors was consistently supported by the multiple studies we reviewed. The association between clinical outcomes and the spectrum of organs/systems affected by irAEs seems to be inconsistent and could be dependent on tumor type. irAEs were associated with a higher ORR and better survival of patients with advanced urothelial cancer treated with pembrolizumab.

Identifiants

pubmed: 32800718
pii: S1558-7673(20)30163-4
doi: 10.1016/j.clgc.2020.07.003
pii:
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
Immune Checkpoint Inhibitors 0
pembrolizumab DPT0O3T46P

Types de publication

Journal Article Review Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

208-216.e1

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Auteurs

Toshiki Kijima (T)

Department of Urology, Tokyo Medical and Dental University Graduate School, Tokyo, Japan. Electronic address: toshiki.kijima@gmail.com.

Hiroshi Fukushima (H)

Department of Urology, Tokyo Medical and Dental University Graduate School, Tokyo, Japan.

Shota Kusuhara (S)

Department of Breast and Medical Oncology, National Cancer Center Hospital East, Chiba, Japan.

Hajime Tanaka (H)

Department of Urology, Tokyo Medical and Dental University Graduate School, Tokyo, Japan.

Soichiro Yoshida (S)

Department of Urology, Tokyo Medical and Dental University Graduate School, Tokyo, Japan.

Minato Yokoyama (M)

Department of Urology, Tokyo Medical and Dental University Graduate School, Tokyo, Japan.

Junichiro Ishioka (J)

Department of Urology, Tokyo Medical and Dental University Graduate School, Tokyo, Japan.

Yoh Matsuoka (Y)

Department of Urology, Tokyo Medical and Dental University Graduate School, Tokyo, Japan.

Noboru Numao (N)

Department of Urology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.

Yasuyuki Sakai (Y)

Department of Urology, Saitama Cancer Center, Saitama, Japan.

Kazutaka Saito (K)

Department of Urology, Tokyo Medical and Dental University Graduate School, Tokyo, Japan.

Nobuaki Matsubara (N)

Department of Breast and Medical Oncology, National Cancer Center Hospital East, Chiba, Japan.

Takeshi Yuasa (T)

Department of Urology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.

Hitoshi Masuda (H)

Department of Urology, National Cancer Center Hospital East, Chiba, Japan.

Junji Yonese (J)

Department of Urology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.

Yukio Kageyama (Y)

Department of Urology, Saitama Cancer Center, Saitama, Japan.

Yasuhisa Fujii (Y)

Department of Urology, Tokyo Medical and Dental University Graduate School, Tokyo, Japan.

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Classifications MeSH