Parnassia Addiction Research Centre (PARC, Brijder Addiction Treatment), The Hague, Netherlands.
Parnassia Addiction Research Centre (PARC, Brijder Addiction Treatment), The Hague, Netherlands.
Lancet. 2016 May 28;387(10034):2226-34. doi: 10.1016/S0140-6736(16)00205-1. Epub 2016 Mar 22.
Heroin-assisted treatment is effective for methadone treatment-refractory heroin-dependent patients, but continued comorbid cocaine dependence remains problematic. Sustained-release dexamfetamine is a promising agonist pharmacotherapy for cocaine dependence and we aimed to assess its acceptance, efficacy, and safety.
In this multicentre, randomised, double-blind, placebo-controlled trial, patients who were treatment-refractory, as indicated by at least two earlier failed treatments aimed at reducing or abstaining from cocaine use, and who regularly (≥8 days/month) used crack-cocaine were enrolled from four heroin-assisted treatment centres in the Netherlands. Eligible patients were randomly assigned (1:1) to receive either 12 weeks of daily, supervised prescription of 60 mg/day oral sustained-release dexamfetamine or placebo in addition to co-prescribed methadone and diacetylmorphine. Randomisation was done by the collaborating pharmacist, using a computer-generated random number sequence with stratification by treatment centre in blocks of four per stratum. Randomisation was masked to patients, staff, and researchers throughout the study. The primary outcome was the number of self-reported days of cocaine use during study treatment, assessed every 4 weeks. Primary and safety analyses were done in the intention-to-treat population. The study was registered with the European Union Drug Regulating Authorities Clinical Trials (EUdraCT 2013-004024-11) and with The Netherlands Trial Register (NTR2576).
Between Aug 8, 2014, and Feb 27, 2015, 111 patients were assessed for eligibility, of whom 73 were enrolled and randomised; 38 patients were assigned to the sustained-release dexamfetamine group and 35 to the placebo group. Sustained-release dexamfetamine treatment resulted in significantly fewer days of cocaine use than placebo treatment (mean 44·9 days [SD 29·4] vs 60·6 days [24·3], respectively [95% CI of difference 3·1-28·4]; p=0·031; Cohen's standardised effect size d=0·58). One or more adverse events were reported by 28 (74%) patients in the dexamfetamine group and by 16 (46%) patients in the placebo group. Most adverse events were transient and well-tolerated.
Sustained-release dexamfetamine is a well accepted, effective, and safe agonist pharmacotherapy for comorbid treatment-refractory cocaine dependence in heroin-dependent patients in heroin-assisted treatment. Future research should aim to replicate these findings in chronic cocaine-dependent and other stimulant-dependent patients in more routine treatment settings, including strategies to optimise treatment adherence like medication management interventions and contingency management.
Netherlands Organisation for Health Research and Development.
海洛因辅助治疗对美沙酮治疗抵抗的海洛因依赖患者有效,但持续存在可卡因共病依赖仍然存在问题。 持续释放型右旋苯丙胺是一种有前途的可卡因依赖激动剂药物治疗方法,我们旨在评估其接受度、疗效和安全性。
在这项多中心、随机、双盲、安慰剂对照试验中,从荷兰的四个海洛因辅助治疗中心招募了治疗抵抗的患者,这些患者至少有两次旨在减少或戒除可卡因使用的先前治疗失败,并且经常(≥8 天/月)使用快克可卡因。符合条件的患者被随机分配(1:1)接受 12 周的每日、监督处方 60mg/天的口服持续释放型右旋苯丙胺或安慰剂,同时给予美沙酮和二乙酰吗啡。随机分配由合作药剂师进行,使用计算机生成的随机数序列,按治疗中心分层,每个分层为 4 个。在整个研究过程中,对患者、工作人员和研究人员均进行了随机分组。主要结局是在研究治疗期间自我报告的可卡因使用天数,每 4 周评估一次。主要和安全性分析均按意向治疗人群进行。该研究已在欧盟药物监管机构临床试验 (EUdraCT 2013-004024-11) 和荷兰试验注册处 (NTR2576) 进行了注册。
在 2014 年 8 月 8 日至 2015 年 2 月 27 日期间,对 111 名患者进行了资格评估,其中 73 名符合条件并被纳入研究;73 名患者中有 38 名被分配到持续释放型右旋苯丙胺组,35 名被分配到安慰剂组。与安慰剂治疗相比,持续释放型右旋苯丙胺治疗导致可卡因使用天数明显减少(平均 44.9 天[SD 29.4] vs 60.6 天[24.3],差异 95%CI 为 3.1-28.4;p=0.031;Cohen's 标准化效应大小 d=0.58)。在右旋苯丙胺组中,有 28 名(74%)患者和安慰剂组中有 16 名(46%)患者报告出现 1 种或多种不良事件。大多数不良事件是短暂的且耐受良好的。
在海洛因辅助治疗的海洛因依赖患者中,持续释放型右旋苯丙胺是一种接受度好、有效且安全的治疗共病治疗抵抗性可卡因依赖的激动剂药物治疗方法。未来的研究应旨在在慢性可卡因依赖和其他兴奋剂依赖患者中复制这些发现,并在更常规的治疗环境中,包括优化治疗依从性的策略,如药物管理干预和条件性管理,以复制这些发现。
荷兰健康研究与发展组织。