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Clinicopathological Features of Kidney Injury Related to Immune Checkpoint Inhibitors: A Systematic Review

(1) Background: Despite increasing recognition of immune checkpoint inhibitors (ICIs) and kidney immune-related adverse events (IRAEs), no large-sample studies have assessed the pathological characteristics and outcomes of biopsy-proven kidney IRAEs. (2) Methods: We comprehensively searched PubMed,...

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Autores principales: Xu, Ling-Yi, Zhao, Hai-Ya, Yu, Xiao-Juan, Wang, Jin-Wei, Zheng, Xi-Zi, Jiang, Lei, Wang, Su-Xia, Liu, Gang, Yang, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9964206/
https://www.ncbi.nlm.nih.gov/pubmed/36835884
http://dx.doi.org/10.3390/jcm12041349
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author Xu, Ling-Yi
Zhao, Hai-Ya
Yu, Xiao-Juan
Wang, Jin-Wei
Zheng, Xi-Zi
Jiang, Lei
Wang, Su-Xia
Liu, Gang
Yang, Li
author_facet Xu, Ling-Yi
Zhao, Hai-Ya
Yu, Xiao-Juan
Wang, Jin-Wei
Zheng, Xi-Zi
Jiang, Lei
Wang, Su-Xia
Liu, Gang
Yang, Li
author_sort Xu, Ling-Yi
collection PubMed
description (1) Background: Despite increasing recognition of immune checkpoint inhibitors (ICIs) and kidney immune-related adverse events (IRAEs), no large-sample studies have assessed the pathological characteristics and outcomes of biopsy-proven kidney IRAEs. (2) Methods: We comprehensively searched PubMed, Embase, Web of Science, and Cochrane for case reports, case series, and cohort studies for patients with biopsy-proven kidney IRAEs. All data were used to describe pathological characteristics and outcomes, and individual-level data from case reports and case series were pooled to analyze risk factors associated with different pathologies and prognoses. (3) Results: In total, 384 patients from 127 studies were enrolled. Most patients were treated with PD-1/PD-L1 inhibitors (76%), and 95% presented with acute kidney disease (AKD). Acute tubulointerstitial nephritis/acute interstitial nephritis (ATIN/AIN) was the most common pathologic type (72%). Most patients (89%) received steroid therapy, and 14% (42/292) required RRT. Among AKD patients, 17% (48/287) had no kidney recovery. Analyses of pooled individual-level data from 221 patients revealed that male sex, older age, and proton pump inhibitor (PPI) exposure were associated with ICI-associated ATIN/AIN. Patients with glomerular injury had an increased risk of tumor progression (OR 2.975; 95% CI, 1.176, 7.527; p = 0.021), and ATIN/AIN posed a decreased risk of death (OR 0.164; 95% CI, 0.057, 0.473; p = 0.001). (4) Conclusions: We provide the first systematic review of biopsy-proven ICI-kidney IRAEs of interest to clinicians. Oncologists and nephrologists should consider obtaining a kidney biopsy when clinically indicated.
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spelling pubmed-99642062023-02-26 Clinicopathological Features of Kidney Injury Related to Immune Checkpoint Inhibitors: A Systematic Review Xu, Ling-Yi Zhao, Hai-Ya Yu, Xiao-Juan Wang, Jin-Wei Zheng, Xi-Zi Jiang, Lei Wang, Su-Xia Liu, Gang Yang, Li J Clin Med Systematic Review (1) Background: Despite increasing recognition of immune checkpoint inhibitors (ICIs) and kidney immune-related adverse events (IRAEs), no large-sample studies have assessed the pathological characteristics and outcomes of biopsy-proven kidney IRAEs. (2) Methods: We comprehensively searched PubMed, Embase, Web of Science, and Cochrane for case reports, case series, and cohort studies for patients with biopsy-proven kidney IRAEs. All data were used to describe pathological characteristics and outcomes, and individual-level data from case reports and case series were pooled to analyze risk factors associated with different pathologies and prognoses. (3) Results: In total, 384 patients from 127 studies were enrolled. Most patients were treated with PD-1/PD-L1 inhibitors (76%), and 95% presented with acute kidney disease (AKD). Acute tubulointerstitial nephritis/acute interstitial nephritis (ATIN/AIN) was the most common pathologic type (72%). Most patients (89%) received steroid therapy, and 14% (42/292) required RRT. Among AKD patients, 17% (48/287) had no kidney recovery. Analyses of pooled individual-level data from 221 patients revealed that male sex, older age, and proton pump inhibitor (PPI) exposure were associated with ICI-associated ATIN/AIN. Patients with glomerular injury had an increased risk of tumor progression (OR 2.975; 95% CI, 1.176, 7.527; p = 0.021), and ATIN/AIN posed a decreased risk of death (OR 0.164; 95% CI, 0.057, 0.473; p = 0.001). (4) Conclusions: We provide the first systematic review of biopsy-proven ICI-kidney IRAEs of interest to clinicians. Oncologists and nephrologists should consider obtaining a kidney biopsy when clinically indicated. MDPI 2023-02-08 /pmc/articles/PMC9964206/ /pubmed/36835884 http://dx.doi.org/10.3390/jcm12041349 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Systematic Review
Xu, Ling-Yi
Zhao, Hai-Ya
Yu, Xiao-Juan
Wang, Jin-Wei
Zheng, Xi-Zi
Jiang, Lei
Wang, Su-Xia
Liu, Gang
Yang, Li
Clinicopathological Features of Kidney Injury Related to Immune Checkpoint Inhibitors: A Systematic Review
title Clinicopathological Features of Kidney Injury Related to Immune Checkpoint Inhibitors: A Systematic Review
title_full Clinicopathological Features of Kidney Injury Related to Immune Checkpoint Inhibitors: A Systematic Review
title_fullStr Clinicopathological Features of Kidney Injury Related to Immune Checkpoint Inhibitors: A Systematic Review
title_full_unstemmed Clinicopathological Features of Kidney Injury Related to Immune Checkpoint Inhibitors: A Systematic Review
title_short Clinicopathological Features of Kidney Injury Related to Immune Checkpoint Inhibitors: A Systematic Review
title_sort clinicopathological features of kidney injury related to immune checkpoint inhibitors: a systematic review
topic Systematic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9964206/
https://www.ncbi.nlm.nih.gov/pubmed/36835884
http://dx.doi.org/10.3390/jcm12041349
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