首页> 外文期刊>The Lancet >Defibrotide for prophylaxis of hepatic veno-occlusive disease in paediatric haemopoietic stem-cell transplantation: An open-label, phase 3, randomised controlled trial
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Defibrotide for prophylaxis of hepatic veno-occlusive disease in paediatric haemopoietic stem-cell transplantation: An open-label, phase 3, randomised controlled trial

机译:去纤蛋白肽在小儿造血干细胞移植中预防肝静脉闭塞性疾病:一项开放标签的3期随机对照试验

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摘要

Background Hepatic veno-occlusive disease is a leading cause of morbidity and mortality after haemopoietic stem-cell transplantation (HSCT). We aimed to assess whether defi brotide can reduce the incidence of veno-occlusive disease in this setting. Methods In our phase 3 open-label, randomised controlled trial, we enrolled patients at 28 European university hospitals or academic medical centres. Eligible patients were younger than 18 years, had undergone myeloablative conditioning before allogeneic or autologous HSCT, and had one or more risk factor for veno-occlusive disease based on modifi ed Seattle criteria. We centrally assigned eligible participants on the basis of a computer-generated randomisation sequence (1:1), stratifi ed by centre and presence of osteopetrosis, to receive intravenous defi brotide prophylaxis (treatment group) or not (control group). The primary endpoint was incidence of veno-occlusive disease by 30 days after HSCT, adjudicated by a masked, independent review committee, in eligible patients who consented to randomisation (intention-to-treat popu lation), and was assessed with a competing risk approach. Patients in either group who developed veno-occlusive disease received defi brotide for treatment. We assessed adverse events to 180 days after HSCT in all patients who received allocated prophylaxis. This trial is registered with ClinicalTrials.gov, number NCT00272948. Findings Between Jan 25, 2006, and Jan 29, 2009, we enrolled 356 eligible patients to the intention-to-treat population. 22 (12%) of 180 patients randomly allocated to the defi brotide group had veno-occlusive disease by 30 days after HSCT compared with 35 (20%) of 176 controls (risk diff erence-7.7%, 95% CI-15.3 to-0.1; Z test for competing risk analysis p=0.0488; log-rank test p=0.0507). 154 (87%) of 177 patients in the defi brotide group had adverse events by day 180 compared with 155 (88%) of 176 controls. Interpretation Defi brotide prophylaxis seems to reduce incidence of veno-occlusive disease and is well tolerated. Thus, such prophylaxis could present a useful clinical option for this serious complication of HSCT. Funding Gentium SpA, European Group for Blood and Marrow Transplantation.
机译:背景肝静脉闭塞性疾病是造血干细胞移植(HSCT)后发病和死亡的主要原因。我们的目的是评估在这种情况下,溴乙锭是否可以减少静脉阻塞性疾病的发生率。方法在我们的3期开放标签,随机对照试验中,我们纳入了28家欧洲大学医院或学术医学中心的患者。符合条件的患者年龄小于18岁,在同种异体或自体HSCT之前接受过清髓处理,并且根据经修改的Seattle标准具有静脉阻塞性疾病的一种或多种危险因素。我们根据计算机生成的随机序列(1:1)(以中心和骨质疏松症分层)为基础,对符合条件的参与者进行了集中分配,以接受静脉给予去溴酸盐预防(治疗组)或不接受(治疗组)。主要终点是HSCT后30天静脉闭塞性疾病的发生率,由蒙面的独立审查委员会裁定,对同意进行随机分组(意向性治疗人群)的合格患者进行评估,并采用竞争风险方法进行评估。两组中发生静脉闭塞性疾病的患者均接受了溴乙锭治疗。我们评估了接受预防性治疗的所有患者在HSCT后180天的不良事件。该试验已在ClinicalTrials.gov上注册,编号为NCT00272948。结果在2006年1月25日至2009年1月29日之间,我们纳入了356例符合意向治疗人群的合格患者。 HSCT后30天,随机分配给去甲溴酸盐组的180例患者中有22例(12%)患有静脉闭塞性疾病,而176例对照中的35例(20%)有静脉阻塞性疾病(风险差异-7.7%,95%CI-15.3至- 0.1;竞争风险分析的Z检验p = 0.0488;对数秩检验p = 0.0507)。到180天时,去甲溴化物组中177名患者中有154名(87%)出现不良事件,而176名对照组中有155名(88%)。解释预防Defi溴化物似乎可以减少静脉阻塞性疾病的发生率,并且耐受性良好。因此,这种预防可能为HSCT的这种严重并发症提供有用的临床选择。欧洲血液和骨髓移植组织Gentium SpA的资金支持。

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