Philips Ashwin, Radhakrishnan Venkatraman, Ganesan Prasanth, Ganesan T S, Ramamurthy Jaikumar, Dhanushkodi Manikandan, Sagar T G
Department of Medical Oncology, Cancer Institute (WIA), Adyar, Chennai, Tamilnadu India.
Indian J Hematol Blood Transfus. 2018 Oct;34(4):618-622. doi: 10.1007/s12288-018-0938-9. Epub 2018 Mar 3.
Rasburicase is a recombinant urate oxidase enzyme approved for use in tumor lysis syndrome (TLS) and it acts by reducing serum uric acid levels. Using rasburicase at the recommended dose of 0.2 mg/kg/day for 5 days is expensive and it is not known whether this extended schedule is clinically beneficial compared to a single fixed dose of 1.5 mg. The aim of the present study was to evaluate the efficacy of single dose rasburicase 1.5 mg in prevention and management of TLS. Rasburicase is available as single use 1.5 mg vial. At our institution a single dose of rasburicase 1.5 mg irrespective of bodyweight has been used in adults and in children a dose of 0.15 mg/kg (maximum 1.5 mg) has been used since 2012 for prevention and management of TLS and subsequent doses are given based on biochemical response and clinical condition. We retrospectively analysed the case records of patients who had received rasburicase from January 2012 to January 2017. The study included 186 patients with hematological malignancies who received rasburicase. Children accounted for 56.4% (n = 105) patients and males comprised 73% (n = 135). Rasburicase was used prophylactically in 59 (31.7%) patients, for laboratory TLS in 76 patients (40.8%) and for clinical TLS in 51 (27.4%) patients. Single fixed dose rasburicase prevented laboratory/clinical TLS in 87% of the prophylactic group and prevented clinical TLS in 72% of the laboratory TLS group. None of the patients in prophylactic and laboratory TLS group developed clinical TLS. However, majority of the patients with clinical TLS required more than one dose rasburicase. Single dose of 1.5 mg (1 vial) rasburicase is efficient in preventing and managing laboratory TLS and is economically viable in resource constrained settings.
拉布立酶是一种重组尿酸氧化酶,已被批准用于肿瘤溶解综合征(TLS),其作用是降低血清尿酸水平。以0.2毫克/千克/天的推荐剂量使用拉布立酶5天成本高昂,而且与单次固定剂量1.5毫克相比,这种延长疗程在临床上是否有益尚不清楚。本研究的目的是评估单次剂量1.5毫克拉布立酶预防和治疗TLS的疗效。拉布立酶有单次使用的1.5毫克小瓶剂型。在我们机构,自2012年以来,成人使用单次剂量1.5毫克拉布立酶(不论体重),儿童使用0.15毫克/千克(最大剂量1.5毫克)用于预防和治疗TLS,后续剂量根据生化反应和临床状况给予。我们回顾性分析了2012年1月至2017年1月接受拉布立酶治疗的患者的病历。该研究包括186例接受拉布立酶治疗的血液系统恶性肿瘤患者。儿童占56.4%(n = 105),男性占73%(n = 135)。59例(31.7%)患者预防性使用拉布立酶,76例(40.8%)患者用于实验室TLS,51例(27.4%)患者用于临床TLS。单次固定剂量拉布立酶在87%的预防组中预防了实验室/临床TLS,在72%的实验室TLS组中预防了临床TLS。预防组和实验室TLS组中均无患者发生临床TLS。然而,大多数临床TLS患者需要不止一剂拉布立酶。单次剂量1.5毫克(1小瓶)拉布立酶在预防和治疗实验室TLS方面有效,且在资源有限的环境中具有经济可行性。