Latha S M, Krishnaprasadh D, Murugapriya P, Scott J X
Department of Paediatrics, Division of Pediatric Hemato Oncology, Sri Ramachandra Medical Centre, Pour, Chennai, Tamil Nadu, India.
Indian J Nephrol. 2015 Mar-Apr;25(2):91-4. doi: 10.4103/0971-4065.139092.
Tumor lysis syndrome (TLS) occurs in malignancies with high proliferative potential and tumor burden, such as lymphomas and leukemias. TLS syndrome is an oncologic emergency, requiring prompt intervention. The metabolic derangements cause acute kidney failure and may lead to cardiac arrhythmias, seizures, and death. With the advent of rasburicase, a recombinant urate oxidase, there has been a decline in the TLS-mediated renal failure and the need for dialysis. The recommended regimen and doses pose a heavy financial burden for patients in developing countries like India. With data and studies proving a similar efficacy for the reduced dose and lesser number of rasburicase, we report here a case series of seven children with acute leukemias, whose TLS was managed by a single dose of rasburicase. A retrospective analysis of case records of seven children with acute lymphoblastic leukemia and TLS, admitted to our Pediatric Oncology Unit of our Hospital between the period 2011 and 2013, was done. All our patients responded to a single dose, indicating that in appropriately monitored patients, single dose followed by as-needed dosing can be cost-saving.
肿瘤溶解综合征(TLS)发生于具有高增殖潜能和肿瘤负荷的恶性肿瘤,如淋巴瘤和白血病。TLS综合征是一种肿瘤急症,需要及时干预。代谢紊乱会导致急性肾衰竭,并可能引发心律失常、癫痫发作甚至死亡。随着重组尿酸氧化酶拉布立酶的出现,TLS介导的肾衰竭及透析需求有所下降。推荐的治疗方案和剂量给印度等发展中国家的患者带来了沉重的经济负担。鉴于数据和研究证明减少剂量及减少拉布立酶使用次数具有相似疗效,我们在此报告一组7例急性白血病患儿的病例系列,他们的TLS通过单剂量拉布立酶得到控制。对2011年至2013年期间入住我院儿科肿瘤科的7例急性淋巴细胞白血病合并TLS患儿的病例记录进行了回顾性分析。我们所有的患者对单剂量治疗均有反应,这表明在适当监测的患者中,单剂量给药后按需给药可节省费用。