Clemmons Amber B, Ensley Elizabeth, Hoge Stephanie, Clark Stephen
University of Georgia College of Pharmacy, Augusta, GA, USA Georgia Regents Medical Center, Augusta, GA, USA
University of Georgia College of Pharmacy, Augusta, GA, USA Georgia Regents Medical Center, Augusta, GA, USA.
Ann Pharmacother. 2014 Sep;48(9):1152-1158. doi: 10.1177/1060028014539144. Epub 2014 Jun 17.
Fixed-dose rasburicase (FDR) is common practice in treating hyperuricemia associated with tumor lysis syndrome in adults; however, there is a lack of data regarding the effectiveness of this dosing strategy specifically in the overweight and obese patient populations.
To determine if patient weight per body mass index (BMI) category is associated with failure of initial FDR as defined by the need for additional dose(s) based on a uric acid level (UAL) ≥7.5 mg/dL within 10 days of previous rasburicase administration.
Adults who received FDR per institutional guidelines from October 2008 to August 2013 were reviewed. Patients had either a baseline UAL ≥7.5 mg/dL or were considered high risk (leukemia or lymphoma diagnosis with white blood cell count >50 000/mm or lactate dehydrogenase level greater than 2 times the upper limit of normal). Patients were stratified by BMI as underweight (<18.5), normal (18.5-24.9), overweight (25-29.9), or obese (30+).
Overall, 12 out of 151 patients who received FDR required a repeat dose of rasburicase. The percentage of patients requiring a repeat rasburicase dose was not different between obese/overweight versus normal/underweight patients (8.7% vs 6.4%, P = 0.75). Similarly, there was no difference between obese alone versus normal/underweight patients (12.3% vs 6.4%; P = 0.51).
In this retrospective analysis, patient BMI did not correlate with failure of FDR in adults, suggesting that this dosing strategy is efficacious in the adult population.
固定剂量的拉布立酶(FDR)是治疗成人肿瘤溶解综合征相关高尿酸血症的常用方法;然而,关于这种给药策略在超重和肥胖患者群体中的有效性的数据却很缺乏。
根据前次拉布立酶给药后10天内尿酸水平(UAL)≥7.5mg/dL而需要额外剂量来定义初始FDR失败,确定按体重指数(BMI)分类的患者体重是否与之相关。
回顾了2008年10月至2013年8月期间按照机构指南接受FDR治疗的成人患者。患者基线UAL≥7.5mg/dL或被认为是高危患者(白血病或淋巴瘤诊断且白细胞计数>50000/mm或乳酸脱氢酶水平大于正常上限的2倍)。患者按BMI分层为体重过轻(<18.5)、正常(18.5 - 24.9)、超重(25 - 29.9)或肥胖(30+)。
总体而言,151例接受FDR治疗的患者中有12例需要重复剂量的拉布立酶。肥胖/超重患者与正常/体重过轻患者之间需要重复拉布立酶剂量的患者百分比没有差异(8.7%对6.4%,P = 0.75)。同样,单纯肥胖患者与正常/体重过轻患者之间也没有差异(12.3%对6.4%;P = 0.51)。
在这项回顾性分析中,患者BMI与成人FDR失败无关,这表明这种给药策略在成人人群中是有效的。