Adverse Events of Immune Checkpoint Inhibitors Therapy for Urologic Cancer Patients in Clinical Trials: A Collaborative Systematic Review and Meta-analysis.

Adverse events Bladder Immune checkpoint inhibitors Immunotherapy Prostate cancer Renal cell carcinoma Renal pelvis Trials Ureter Urology Urothelial carcinoma

Journal

European urology
ISSN: 1873-7560
Titre abrégé: Eur Urol
Pays: Switzerland
ID NLM: 7512719

Informations de publication

Date de publication:
Apr 2022
Historique:
received: 10 11 2021
revised: 23 12 2021
accepted: 13 01 2022
pubmed: 2 2 2022
medline: 19 4 2022
entrez: 1 2 2022
Statut: ppublish

Résumé

Therapies based on immune checkpoint inhibitors (ICIs) are transforming the treatment landscape of urologic oncology. Nevertheless, an exhaustive overview of the toxicity spectrum of these novel therapies has yet to be provided. To comprehensively investigate the incidence and profile of ICI therapy-related adverse events (AEs) across urologic cancers. We searched for all clinical trials investigating the role of ICI therapy published between January 2010 and September 2021. Studies involving urologic cancers with reported overall incidence or tabulated data of treatment-related AEs (trAEs) or immune-related AEs (irAEs) were included. A systematic review and meta-analysis was performed after protocol registration in PROSPERO (CRD42021276435). We identified 2638 records, of which 92 studies (including 22942 participants) met the inclusion criteria. The pooled overall incidence was 81.6% (95% confidence interval [CI] 78.0-84.7) for any-grade trAEs and 29.3% (95% CI 24.9-34.1) for grade ≥3 trAEs. The pooled overall incidence was 34.3% (95% CI 28.5-40.7) for any-grade irAEs and 10.2% (95%CI 8.2-12.7) for grade ≥3 irAEs. On a multivariable analysis, cancer type, therapy combination, clinical settings (perioperative vs advanced/metastatic), and drug exposure were independently associated with the occurrence of trAEs or irAEs. The overall rate of treatment-related mortality was 0.94% (140 of 14 899 participants), with pneumonitis (9.3%), pneumonia (7.9%), and respiratory failure (7.1%) being the most common causes. Immune-related mortality occurred in 0.26% (28 of 10 723) patients, with pneumonitis (35.7%), hepatic failure (10.7%), and hepatitis (7.1%) being most common. Our study provides a comprehensive overview of ICI-associated AEs in urologic cancer patients. The spectrum and incidence of AEs vary across cancer types, ICI types, clinical settings, and therapy combinations. These findings provide important guidance to clinicians in counseling and management of patients with urologic cancers. A high proportion of patients experience immune checkpoint inhibitor-associated toxicity. Physician and patient education is critical for early recognition and proper management.

Identifiants

pubmed: 35101302
pii: S0302-2838(22)00065-3
doi: 10.1016/j.eururo.2022.01.028
pii:
doi:

Substances chimiques

Immune Checkpoint Inhibitors 0

Types de publication

Journal Article Meta-Analysis Research Support, Non-U.S. Gov't Review Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

414-425

Informations de copyright

Copyright © 2022 The Author(s). Published by Elsevier B.V. All rights reserved.

Auteurs

Zhenjie Wu (Z)

Department of Urology, Changhai Hospital, Naval Medical University, Shanghai, China.

Qi Chen (Q)

Department of Health Statistics, Naval Medical University, Shanghai, China.

Le Qu (L)

Department of Urology, Jinling Hospital, Clinical School of Medical College, Nanjing University, Nanjing, China. Electronic address: septsoul@hotmail.com.

Mingmin Li (M)

Department of Radiology, Changhai Hospital, Naval Medical University, Shanghai, China. Electronic address: limingmin421@sina.com.

Linhui Wang (L)

Department of Urology, Changhai Hospital, Naval Medical University, Shanghai, China. Electronic address: wanglinhui@smmu.edu.cn.

Maria C Mir (MC)

Department of Urology, Valencian Oncology Institute Foundation, FIVO, Valencia, Spain.

Umberto Carbonara (U)

Department of Urology, Aldo Moro University, Bari, Italy.

Savio D Pandolfo (SD)

Division of Urology, VCU Health System, Richmond, VA, USA.

Peter C Black (PC)

Department of Urologic Sciences, The University of British Columbia, Vancouver, British Columbia, Canada.

Asit K Paul (AK)

Division of Hematology, Oncology and Palliative Care, Department of Internal Medicine, VCU Massey Cancer Center, Virginia Commonwealth University, Richmond, VA, USA.

Giuseppe Di Lorenzo (G)

Oncology Unit, Andrea Tortora Hospital, ASL Salerno, Pagani, Italy; Vincenzo Tiberio Department of Medicine and Health Sciences, University of Molise, Campobasso, Italy.

Francesco Porpiglia (F)

Department of Urology, San Luigi Gonzaga Hospital, University of Turin, Orbassano, Italy.

Andrea Mari (A)

Department of Clinical and Experimental Medicine, University of Florence. Unit of Oncologic Minimally-Invasive Urology and Andrology, Careggi Hospital, Florence, Italy.

Andrea Necchi (A)

Genitourinary Medical Oncology, IRCCS San Raffaele Hospital and Scientific Institute, Milan, Italy.

Morgan Rouprêt (M)

Department of Urology, GRC n°5, Predictive Onco-Uro, AP-HP, Hôpital Pitié-Salpêtrière, Sorbonne University, Paris, France.

Sarah P Psutka (SP)

Department of Urology, University of Washington, Seattle Cancer Care Alliance, Seattle, WA, USA.

Riccardo Autorino (R)

Division of Urology, VCU Health System, Richmond, VA, USA.

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Classifications MeSH