Hôpital Paul Brousse, INSERM 669, Université Paris-Sud, Villejuif, France.
Drug Alcohol Depend. 2013 Nov 1;133(1):15-29. doi: 10.1016/j.drugalcdep.2013.04.025. Epub 2013 Jun 6.
European Medicines Agency guidelines recognize two different treatment goals for alcohol dependence: abstinence and reduction in alcohol consumption. All currently approved agents are indicated for abstinence. This systematic review aimed to identify drugs in development for alcohol dependence treatment and to establish, based upon trial design, if any are seeking market authorization for reduction in consumption.
We searched PubMed and Embase (December 2001-November 2011) to identify agents in development for alcohol dependence treatment. Additional studies were identified by searching ClinicalTrials.gov and the R&D Insight and Clinical Trials Insight databases. Studies in which the primary focus was treatment of comorbidity, or n≤20, were excluded. Studies were then classified as 'abstinence' if they: described a detoxification/alcohol withdrawal period; enrolled patients who had undergone detoxification previously; or presented relapse/abstinence rates as the primary outcome. Studies in patients actively drinking at baseline were classified as 'reduction in consumption'.
Of 602 abstracts identified, 45 full-text articles were eligible. Five monotherapies were in development for alcohol dependence treatment: topiramate, fluvoxamine, aripiprazole, flupenthixol and nalmefene. Nalmefene was the only agent whose sponsor was clearly seeking definitive approval for reduction in consumption. Development status was unclear for topiramate, fluvoxamine, aripiprazole and flupenthixol. Fifteen agents were examined in published exploratory investigator-initiated trials; the majority focused on abstinence. Ongoing (unpublished) trials tended to focus on reduction in consumption.
While published studies generally focused on abstinence, ongoing trials focused on reduction in consumption, suggesting a change in emphasis in the approach to treating alcohol dependence.
欧洲药品管理局指南承认酒精依赖的两种不同治疗目标:戒除和减少饮酒量。目前所有批准的药物都适用于戒除。本系统评价旨在确定正在开发用于治疗酒精依赖的药物,并根据试验设计确定是否有任何药物正在寻求减少消费的市场授权。
我们搜索了 PubMed 和 Embase(2001 年 12 月至 2011 年 11 月),以确定正在开发用于治疗酒精依赖的药物。通过搜索 ClinicalTrials.gov 和 R&D Insight 和 Clinical Trials Insight 数据库,发现了其他研究。主要关注共病治疗或 n≤20 的研究被排除在外。如果研究的主要重点是治疗共病,或 n≤20,则将研究归类为“戒除”:描述了脱毒/酒精戒断期;招募了以前接受过脱毒治疗的患者;或将复发/戒除率作为主要结果。在基线时积极饮酒的患者的研究被归类为“减少饮酒量”。
在 602 篇摘要中,有 45 篇全文文章符合条件。有 5 种单药疗法正在开发用于治疗酒精依赖:托吡酯、氟伏沙明、阿立哌唑、氟奋乃静和纳美芬。纳美芬是唯一一种其赞助商明确寻求减少消费的明确批准的药物。托吡酯、氟伏沙明、阿立哌唑和氟奋乃静的开发状况尚不清楚。在已发表的探索性研究者发起的试验中检查了 15 种药物;大多数都集中在戒除上。正在进行的(未发表)试验往往侧重于减少消费。
虽然已发表的研究通常侧重于戒除,但正在进行的试验侧重于减少消费,这表明在治疗酒精依赖的方法上强调的重点发生了变化。