4.6 Review

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

Journal

EUROPEAN UROLOGY
Volume 81, Issue 4, Pages 414-425

Publisher

ELSEVIER
DOI: 10.1016/j.eururo.2022.01.028

Keywords

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

Funding

  1. National Natural Science Foundation of China [82072825, 81874093, 81730073, 81872074, 81772740, 82173345]
  2. Program of Shanghai Municipal Health Bureau (Hospital New Star Program of Shanghai)
  3. Foundation for Distinguished Youths of Jiangsu Province [BK20200006]
  4. Shanghai Sail Program [19YF1459200]

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This study comprehensively investigated the incidence and profile of adverse events associated with immune checkpoint inhibitor therapy in urologic cancer patients. The findings revealed variations in the spectrum and incidence of adverse events across different cancer types, immune checkpoint inhibitor types, clinical settings, and therapy combinations.
Context: 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. Objective: To comprehensively investigate the incidence and profile of ICI therapy-related adverse events (AEs) across urologic cancers. Evidence acquisition: 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). Evidence synthesis: We identified 2638 records, of which 92 studies (including 22 942 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. Conclusions: 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. Patient summary: A high proportion of patients experience immune checkpoint inhibitor-associated toxicity. Physician and patient education is critical for early recognition and proper management. (C) 2022 The Author(s). Published by Elsevier B.V. on behalf of European Association of Urology.

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