Dhillon Patwant, Amir Eitan, Lo Melissa, Kitchlu Abhijat, Chan Christopher, Cochlin Stephen, Yip Paul, Chen Eric, Lee Roy, Ng Pamela
1 Department of Pharmacy, Princess Margaret Cancer Centre, UHN, Toronto, Canada.
2 Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, UHN, Toronto, Canada.
J Oncol Pharm Pract. 2019 Jun;25(4):875-883. doi: 10.1177/1078155218771461. Epub 2018 May 3.
Mannitol is an osmotic diuretic given routinely as part of cisplatin regimens to prevent nephrotoxicity, but there are limited data on the ideal dosage. At our center, three different doses of mannitol are used: 12, 20, and 40 g per cycle for cisplatin doses of ≥50 mg/m. The primary objective was to determine if variations in mannitol dosing significantly influence the incidence of cisplatin-induced acute nephrotoxicity.
A case-control study was performed. Electronic records of 1462 consecutive outpatients who received cisplatin at ≥ 50 mg/m per cycle between January 2010 and December 2014 were reviewed. Patients experiencing nephrotoxicity of any grade within 30 days of last cisplatin dose, as defined by NCI CTCAE 4.0, were matched to a minimum of two and maximum of five controls based on the following criteria: age ± 5 years, baseline estimated glomerular filtration rate ± 10 ml/min/1.73 m, cisplatin dose per cycle, and presence of diabetes. Conditional logistic regression was used to identify baseline predictors of cisplatin-induced acute nephrotoxicity.
Of the 1245 included patients, 237 had nephrotoxicity and 1008 were matched controls. Median baseline estimated glomerular filtration rate for cases and controls were 83 and 80 ml/min/1.73 m, respectively. A total of 3.8% of cases experienced ≥ grade 3 nephrotoxicity. Univariable analysis showed that diabetes, lymphoma, low baseline estimated glomerular filtration rate, and low baseline magnesium level were significantly associated with nephrotoxicity, whereas mannitol dosing did not show any association (odds ratio 1.08; p = 0.29). In multivariable analysis, diabetes and lymphoma retained statistical significance, but baseline estimated glomerular filtration rate and baseline magnesium level showed nonsignificant associations with nephrotoxicity.
Cisplatin-induced acute nephrotoxicity remains common in patients with good baseline renal function despite preventive measures. Diabetes and lymphoma are predictors of nephrotoxicity, whereas mannitol dosing has no significant influence, suggesting that doses may be standardized across cisplatin regimens.
甘露醇是一种渗透性利尿剂,在顺铂治疗方案中常规使用以预防肾毒性,但关于理想剂量的数据有限。在我们中心,使用三种不同剂量的甘露醇:对于顺铂剂量≥50mg/m²,每周期分别为12g、20g和40g。主要目的是确定甘露醇剂量的变化是否会显著影响顺铂诱导的急性肾毒性的发生率。
进行了一项病例对照研究。回顾了2010年1月至2014年12月期间连续接受每周期≥50mg/m²顺铂治疗的1462例门诊患者的电子记录。根据美国国立癌症研究所(NCI)癌症治疗不良反应评价标准(CTCAE)4.0定义,在最后一剂顺铂后30天内出现任何级别的肾毒性的患者,根据以下标准与至少2例且最多5例对照进行匹配:年龄±5岁、基线估计肾小球滤过率±10ml/min/1.73m²、每周期顺铂剂量以及是否患有糖尿病。采用条件逻辑回归分析来确定顺铂诱导的急性肾毒性的基线预测因素。
在纳入的1245例患者中,237例出现肾毒性,1008例为匹配对照。病例组和对照组的基线估计肾小球滤过率中位数分别为83ml/min/1.73m²和80ml/min/1.73m²。共有3.8%的病例出现≥3级肾毒性。单因素分析显示,糖尿病、淋巴瘤、低基线估计肾小球滤过率和低基线镁水平与肾毒性显著相关,而甘露醇剂量与肾毒性无任何关联(比值比为1.08;p = 0.29)。多因素分析中,糖尿病和淋巴瘤仍具有统计学意义,但基线估计肾小球滤过率和基线镁水平与肾毒性的关联无统计学意义。
尽管采取了预防措施,但在基线肾功能良好的患者中,顺铂诱导的急性肾毒性仍然常见。糖尿病和淋巴瘤是肾毒性的预测因素,而甘露醇剂量没有显著影响,这表明在顺铂治疗方案中剂量可以标准化。