Risk analysis for cisplatin-induced nephrotoxicity during first cycle of chemotherapy
نویسندگان
چکیده
Although cisplatin is one of the most widely used anticancer drugs, nephrotoxicity remains a major doselimiting side effect. To reduce the incidence of cisplatin-induced nephrotoxicity, we analyzed possible risk factors in 349 patients who received cisplatin (15-120 mg/m2) for the first cycle of chemotherapy between April 2011 and March 2014. Nephrotoxicity was defined as serum creatinine elevation > 1.5 times that at baseline (grade ≥ 2) from 4 to 7 days after injection, according to the Common Terminology Criteria for Adverse Events Version 4.0. Dose of cisplatin > 20 mg/m2 significantly increased serum creatinine concentration and caused nephrotoxicity in a dosedependent manner, with a 13.7% incidence of nephrotoxicity (30/219) at doses > 40 mg/m2. A multivariate logistic regression analysis revealed the following as significant risk factors for cisplatin-induced nephrotoxicity: age ≥ 65 years, low serum albumin (≤ 3.5 g/dl), high doses (≥ 80 mg/m2) of cisplatin and the use of mannitol. Risk factors of cisplatin nephrotoxicity were old age, low serum albumin, high dose of cisplatin, and inclusion of mannitol in transfusion. Mannitol should therefore not be included in intravenous hydration. In addition, as the number of risk factors increased, so did the incidence of cisplatin-induced nephrotoxicity.
منابع مشابه
The Effect of Hydration Therapy with and without Magnesium Sulfate on Prevention of Cisplatin-Induced Nephrotoxicity
Background: Cisplatin is an antineoplastic agent used to treat many malignancies; however, the main side effect of cisplatin is nephrotoxicity. The aim of this study was to evaluate the effect of hydration therapy with and without magnesium on prevention of cisplatin-induced nephrotoxicity. Methods: This retrospective study was performed on 46 patients with malignancy who were candidate to rec...
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Cisplatin is a potent chemotherapy agent which is used to treat a broad spectrum of solid cancers. However, its clinical use is limited due to its nephrotoxicity with a decline in the glomerular filtration rate that occur in 15-30% of patients. Multiple mechanisms contribute to renal dysfunction following exposure to cisplatin include tubular epithelial cell toxicity, vasoconstriction in the re...
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