Prevention of Cisplatin-Induced Acute Kidney Injury: A Systematic Review and Meta-Analysis

被引:65
作者
Hamroun, Aghiles [1 ]
Lenain, Remi [1 ]
Bigna, Jean Joel [2 ]
Speyer, Elodie [3 ]
Bui, Linh [4 ]
Chamley, Paul [1 ]
Pottier, Nicolas [5 ]
Cauffiez, Christelle [6 ]
Dewaeles, Edmone [6 ]
Dhalluin, Xavier [7 ]
Scherpereel, Arnaud [7 ]
Hazzan, Marc [1 ,8 ]
Maanaoui, Mehdi [1 ]
Glowacki, Francois [1 ,6 ]
机构
[1] Univ Lille, CHRU Lille, Nephrol Dept, F-59000 Lille, France
[2] Univ Paris Saclay, Fac Med, Paris, France
[3] Versailles St Quentin Univ, Univ Paris Sud, Paris Saclay Univ, INSERM,UMRS 1018,Ctr Res Epidemiol & Populat Hlth, F-94807 Villejuif, France
[4] CH Beuvry, Nephrol Dept, Bethune, France
[5] CHRU Lille, Dept Toxicol & Genet Pathol, F-59000 Lille, France
[6] Univ Lille, Med Fac, Res Dept, EA 4483 IMPECS IMPact Environm Chem Human Hlth, F-59045 Lille, France
[7] Univ Lille, INSERM, U1189, Pulm & Thorac Oncol Dept,OncoThAI, F-59000 Lille, France
[8] INSERM, UMR995, F-59000 Lille, France
关键词
PATIENTS RECEIVING CISPLATIN; ORGANIC CATION TRANSPORTER-2; INDUCED NEPHROTOXICITY; CANCER-PATIENTS; GENETIC-VARIANTS; RISK-FACTORS; INDUCED TOXICITIES; CLINICAL-TRIALS; RENAL TOXICITY; OVARIAN-CANCER;
D O I
10.1007/s40265-019-01182-1
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Purpose Cisplatin-induced acute kidney injury (CIA) is a serious adverse event that affects 20-40% of exposed patients, despite any implemented precaution to avoid it. The aim of this work was therefore to identify a relevant nephroprotective method for CIA. Methods We searched Pubmed, Embase, and Web of Science from 1 January 1978 to 1 June 2018, without language restriction. All studies (observational and interventional) assessing a CIA prevention method for adults receiving at least one course of cisplatin were eligible. The primary outcome was acute nephrotoxicity, as defined by the AKI-KDIGO classification (2012). The odds ratio and corresponding 95% confidence interval were used to assess the associations. We used narrative synthesis in case of heterogeneity regarding intervention, population, or outcome. When possible, a random-effects model was used to pool studies. The heterogeneity between studies was quantified (I-2), and multiple meta-regressions were carried out to identify potential confounders. Results Within 4520 eligible studies, 51 articles fulfilling the selection criteria were included in the review, assessing 21 different prevention methods. A meta-analysis could only be performed on the 15 observational studies concerning magnesium supplementation (1841 patients), and showed a significant nephroprotective effect for all combined grades of CIA (OR 0.24, [0.19-0.32], I-2 = 0.0%). This significant nephroprotective effect was also observed for grades 2 and 3 CIA (OR 0.22, [0.14-0.33], I-2 = 0.0% and OR 0.25, [0.08-0.76], I-2 = 0.0%, respectively). Conclusion While no method of prevention had so far demonstrated its indisputable efficacy, our results highlight the potential protective effect of magnesium supplementation on cisplatin-induced acute nephrotoxicity.
引用
收藏
页码:1567 / 1582
页数:16
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