Abstract

BackgroundCisplatin is a highly effective chemotherapeutic agent. However, acute kidney injury (AKI) limits its subsequent use, resulting in poor cancer prognosis. Dipeptidyl peptidase-4 (DPP-4) inhibitors have been reported to attenuate cisplatin-induced AKI in animal models, but the effect in human patients remains to be clarified. We hypothesized that DPP-4 inhibitors can prevent cisplatin-induced AKI in diabetic-cancer patients.MethodsWe retrospectively reviewed all consecutive cancer patients who were treated with a first cycle of cisplatin-containing regimen between January 2011 and October 2019. We analysed data of diabetic-cancer patients treated with high-dose cisplatin (> 50 mg/m2)-containing regimens. The change of estimated glomerular filtration rate (eGFR) within 2 weeks after cisplatin treatment was compared between the patients treated with DPP-4 inhibitors and those treated without DPP-4 inhibitors.ResultsA total of 455 patients were treated with cisplatin during the period. Of these, 34 patients were eligible for the analysis. The change of eGFR was significantly less in the patients treated with DPP-4 inhibitors, compared to those without DPP-4 inhibitors [the percentages of eGFR decline (mean ± SD) was 23.6 ± 20.3% vs 43.1± 20.1%, respectively; P = 0.010]. Furthermore, the incidence of AKI was significantly less in the patients treated with DPP-4 inhibitors (25% vs 64%, respectively; P = 0.026).ConclusionsDPP-4 inhibitors may decrease the risk of cisplatin-induced AKI in diabetic patients.

Highlights

  • Cisplatin is one of the widely used chemotherapeutic agents for many types of malignancies, but frequently induces acute kidney injury (AKI)

  • The incidence of AKI was significantly less in the patients treated with Dipeptidyl peptidase-4 (DPP-4) inhibitors (25% vs 64%, respectively; P = 0.026)

  • DPP-4 inhibitors may decrease the risk of cisplatin-induced AKI in diabetic patients

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Summary

Introduction

Cisplatin is one of the widely used chemotherapeutic agents for many types of malignancies, but frequently induces acute kidney injury (AKI). It has been reported that DPP-4 inhibitors can prevent AKI induced by ischemia-reperfusion and chronic kidney injury in several animal models [6,7,8,9,10]. It remains to be investigated whether DPP-4 inhibitors can attenuate kidney injury in human patients. Dipeptidyl peptidase-4 (DPP4) inhibitors have been reported to attenuate cisplatin-induced AKI in animal models, but the effect in human patients remains to be clarified. We hypothesized that DPP-4 inhibitors can prevent cisplatin-induced AKI in diabetic-cancer patients

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