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首页> 外文期刊>Lancet Neurology >Lithium in patients with amyotrophic lateral sclerosis (LiCALS): a phase 3 multicentre, randomised, double-blind, placebo-controlled trial.
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Lithium in patients with amyotrophic lateral sclerosis (LiCALS): a phase 3 multicentre, randomised, double-blind, placebo-controlled trial.

机译:肌萎缩性侧索硬化症(LiCALS)患者中的锂:3期多中心,随机,双盲,安慰剂对照试验。

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Lithium has neuroprotective effects in cell and animal models of amyotrophic lateral sclerosis (ALS), and a small pilot study in patients with ALS showed a significant effect of lithium on survival. We aimed to assess whether lithium improves survival in patients with ALS.The lithium carbonate in amyotrophic lateral sclerosis (LiCALS) trial is a randomised, double-blind, placebo-controlled trial of oral lithium taken daily for 18 months in patients with ALS. Patients aged at least 18 years who had ALS according to the revised El Escorial criteria, had disease duration between 6 and 36 months, and were taking riluzole were recruited from ten centres in the UK. Patients were randomly assigned (1:1) to receive either lithium or matched placebo tablets. Randomisation was via an online system done at the level of the individual by block randomisation with randomly varying block sizes, stratified by study centre and site of disease onset (limb or bulbar). All patients and assessing study personnel were masked to treatment assignment. The primary endpoint was the rate of survival at 18 months and was analysed by intention to treat. This study is registered with Eudract, number 2008-006891-31.Between May 26, 2009, and Nov 10, 2011, 243 patients were screened, 214 of whom were randomly assigned to receive lithium (107 patients) or placebo (107 patients). Two patients discontinued treatment and one died before the target therapeutic lithium concentration could be achieved. 63 (59%) of 107 patients in the placebo group and 54 (50%) of 107 patients in the lithium group were alive at 18 months. The survival functions did not differ significantly between groups (Mantel-Cox log-rank χ(2) on 1 df=1·64; p=0·20). After adjusting for study centre and site of onset using logistic regression, the relative odds of survival at 18 months (lithium vs placebo) was 0·71 (95% CI 0·40-1·24). 56 patients in the placebo group and 61 in the lithium group had at least one serious adverse event.We found no evidence of benefit of lithium on survival in patients with ALS, but nor were there safety concerns, which had been identified in previous studies with less conventional designs. This finding emphasises the importance of pursuing adequately powered trials with clear endpoints when testing new treatments.The Motor Neurone Disease Association of Great Britain and Northern Ireland.
机译:锂在肌萎缩性侧索硬化症(ALS)的细胞和动物模型中具有神经保护作用,一项针对ALS患者的小型先导研究表明锂对存活率具有显着影响。我们旨在评估锂是否能改善ALS患者的生存率。肌萎缩性侧索硬化症(LiCALS)试验中的碳酸锂是一项随机,双盲,安慰剂对照试验,每天口服18个月的ALS患者锂。从英国的十个中心招募了至少18岁,根据修订的El Escorial标准患有ALS,病程在6到36个月之间并且正在服用利鲁唑的患者。患者被随机分配(1:1)接受锂或匹配的安慰剂片剂。随机化是通过在线系统在个人水平上进行的,该系统通过随机分组的大小随机分组,按研究中心和疾病发作部位(肢体或延髓)进行分层。所有患者和评估研究人员都被掩盖了治疗分配。主要终点是18个月生存率,并按治疗意愿进行分析。该研究已在Eudract注册,编号为2008-006891-31.2009年5月26日至2011年11月10日之间,筛选了243例患者,其中214例被随机分配接受锂(107例)或安慰剂(107例) 。两名患者停止治疗,一名患者在达到目标治疗锂浓度之前死亡。安慰剂组的107名患者中有63名(59%),锂组的107名患者中有54名(50%)存活了18个月。各组之间的生存功能无显着差异(Mantel-Cox log-rankχ(2)在1 df = 1·64; p = 0·20)。使用logistic回归调整研究中心和发作部位后,18个月生存的相对几率(锂与安慰剂)为0·71(95%CI 0·40-1·24)。安慰剂组的56例患者和锂盐组的61例患者至少发生了一次严重不良事件。我们没有发现锂对ALS患者生存的益处,也没有安全性担忧,先前的研究已经证实较不常规的设计。这一发现强调了在测试新疗法时进行具有明确终点的充分试验的重要性。大不列颠及北爱尔兰运动神经元疾病协会。

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