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Evaluation of Urinary Neutrophil Gelatinase-Associated Lipocalin and Urinary Kidney Injury Molecule-1 As Biomarkers of Renal Function in Cancer Patients Treated With Cisplatin Publisher Pubmed



Ghadrdan E1 ; Ebrahimpour S2 ; Sadighi S3 ; Chaibakhsh S4, 5 ; Jahangardrafsanjani Z1
Authors
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Authors Affiliations
  1. 1. Department of Clinical Pharmacy. Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran
  2. 2. Department of Clinical Pharmacy, Virtual University of Medical Sciences, Tehran, Iran
  3. 3. Cancer Institute, Tehran University of Medical Sciences, Tehran, Iran
  4. 4. Resaerch Center for Rational Use of Drugs, Tehran University of Medical Sciences, Tehran, Iran
  5. 5. Neuromusculoskeletal Research Center, Iran University of Medical Sciences, Tehran, Iran

Source: Journal of Oncology Pharmacy Practice Published:2020


Abstract

Introduction: Cisplatin-associated acute kidney injury (AKI) is the major limitation to the use of cisplatin-based chemotherapy regimens. Serum creatinine as a traditional marker did not increase in a timely enough fashion in AKI patients. Therefore, recently, the novel markers such as neutrophil gelatinase-associated lipocalin (NGAL) and kidney injury molecule-1 (KIM-1) were considered for early detection of AKI. The aim of this study was to compare the sensitivity and specificity of urinary NGAL and KIM-1 with serum creatinine in cisplatin related AKI. Methods: Patients ≥18 years with solid tumors who received cisplatin-based chemotherapy were included. Urine samples were collected 0, 6 and 24 h after cisplatin infusion and the urinary NGAL, KIM-1, and creatinine concentrations were evaluated. NGAL and KIM-1 concentrations were adjusted based on urine creatinine to eliminate hydration effects. Serum creatinine levels were assessed at the base and 72 h after cisplatin administration. Results: Seven out of the 35 recruited patients (20%) suffered from AKI defined by Acute Kidney Injury Network criteria. In AKI patients, the ratio of urinary KIM-1–creatinine at 24 h compared to baseline (24 h/baseline) and NGAL–creatinine 24 h/baseline were significantly higher than those of non-AKI group (p = 0.037 and 0.047 respectively). The area under the receiver-operating characteristic curve for KIM-1–creatinine 24 h/baseline and NGAL–creatinine 24 h/baseline were 0.78 (0.59–0.96, p = 0.032) and 0.77 (0.57–0.97, p = 0.036) respectively. Conclusions: Our findings showed that the changes in urinary NGAL–creatinine and KIM-1–creatinine ratios, 24 h after cisplatin administration can be utilized to predict AKI in cisplatin recipients. © The Author(s) 2020.