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肌萎缩侧索硬化症患者的锂治疗(LiCALS):一项 3 期多中心、随机、双盲、安慰剂对照试验。

Lithium in patients with amyotrophic lateral sclerosis (LiCALS): a phase 3 multicentre, randomised, double-blind, placebo-controlled trial.

出版信息

Lancet Neurol. 2013 Apr;12(4):339-45. doi: 10.1016/S1474-4422(13)70037-1. Epub 2013 Feb 27.

Abstract

BACKGROUND

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.

METHODS

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.

FINDINGS

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.

INTERPRETATION

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.

FUNDING

The Motor Neurone Disease Association of Great Britain and Northern Ireland.

摘要

背景

锂在肌萎缩侧索硬化症(ALS)的细胞和动物模型中具有神经保护作用,一项针对 ALS 患者的小型试点研究表明锂对生存有显著影响。我们旨在评估锂是否能改善 ALS 患者的生存。

方法

碳酸锂治疗肌萎缩侧索硬化症(LiCALS)试验是一项随机、双盲、安慰剂对照试验,对 ALS 患者每日口服锂治疗 18 个月。该试验招募了英国 10 个中心的至少 18 岁、根据修订后的埃尔埃斯科里亚尔标准诊断为 ALS、疾病持续时间为 6 至 36 个月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。随机化通过在线系统进行,以个体为单位,通过具有随机变化的块大小的块随机化进行,按研究中心和疾病发病部位(肢体或球部)分层。所有患者和评估研究人员均对治疗分配进行了盲法。主要终点为 18 个月时的生存率,并通过意向治疗进行分析。该研究在 Eudract 注册,编号为 2008-006891-31。

结果

2009 年 5 月 26 日至 2011 年 11 月 10 日期间,共筛查了 243 名患者,其中 214 名患者被随机分配接受锂(107 名患者)或安慰剂(107 名患者)治疗。2 名患者停止治疗,1 名患者在达到目标治疗锂浓度前死亡。安慰剂组 107 名患者中有 63 名(59%)和锂组 107 名患者中有 54 名(50%)在 18 个月时存活。两组的生存函数无显著差异(Mantel-Cox 对数秩检验,1df=1.64;p=0.20)。使用逻辑回归调整研究中心和发病部位后,18 个月时的生存相对优势(锂与安慰剂)为 0.71(95%CI 0.40-1.24)。安慰剂组 56 名患者和锂组 61 名患者至少发生了 1 次严重不良事件。

结论

我们没有发现锂对 ALS 患者生存有任何益处的证据,但也没有出现之前使用非传统设计进行的研究中发现的安全性问题。这一发现强调了当测试新疗法时,进行具有明确终点的、充分有力的试验的重要性。

资金来源

英国和北爱尔兰运动神经元疾病协会。

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