Reus Victor I, Obach R Scott, Coe Jotham W, Faessel Helene, Rollema Hans, Watsky Eric, Reeves Karen
Department of Psychiatry, University of California School of Medicine, San Francisco, California 94143-0984, USA.
Drugs Today (Barc). 2007 Feb;43(2):65-75. doi: 10.1358/dot.2007.43.2.1069956.
Smoking is a significant public health problem, and existing treatments have demonstrated only moderate efficacy in assisting smokers to quit. Varenicline, recently approved by the U.S. Food and Drug Administration and the European Agency for the Evaluation of Medicinal Products as an aid to smoking cessation treatment, has a novel mechanism of action, targeting the specific nicotinic acetylcholine receptor (nAChR) associated with nicotine-induced behaviors (alpha4beta2 nAChR). It has both agonistic and antagonistic properties that together are believed to account for reduction of craving and withdrawal as well as blocking the rewarding effects of smoking. The clinical efficacy and tolerability of varenicline has been demonstrated in phase III clinical trials involving more than 2,000 cigarette smokers. At the end of the treatment period in two 12-week, multicenter, randomized, double-blind, placebo-controlled studies, patients receiving varenicline (1 mg twice daily) experienced an increase in the odds of quitting smoking by nearly fourfold compared with those receiving placebo, and almost twofold compared with the odds for patients receiving 150 mg bupropion SR (sustained release) twice daily. In these two trials where patients were randomized to either varenicline or bupropion, the efficacy of varenicline was consistently superior at 12 weeks; this result sustained significance at 24 weeks in both studies and up to 52 weeks in one study. Nausea, a common adverse event reported in clinical trials, led to few treatment discontinuations. Its targeted mechanism of action, superior efficacy and excellent tolerability make varenicline a welcome and useful addition to the therapeutic options for smoking cessation.
吸烟是一个重大的公共卫生问题,现有治疗方法在帮助吸烟者戒烟方面仅显示出中等疗效。伐尼克兰最近已获美国食品药品监督管理局和欧洲药品评估局批准,作为戒烟治疗辅助药物,其作用机制新颖,靶向与尼古丁诱导行为相关的特定烟碱型乙酰胆碱受体(α4β2 nAChR)。它同时具有激动和拮抗特性,据信这些特性共同作用可减少烟瘾和戒断反应,并阻断吸烟的奖赏效应。伐尼克兰的临床疗效和耐受性已在涉及2000多名吸烟者的III期临床试验中得到证实。在两项为期12周的多中心、随机、双盲、安慰剂对照研究的治疗期结束时,接受伐尼克兰(每日两次,每次1mg)治疗的患者戒烟几率相比接受安慰剂的患者增加了近四倍,相比每日两次接受150mg缓释安非他酮的患者增加了近两倍。在这两项将患者随机分为接受伐尼克兰或安非他酮治疗的试验中,伐尼克兰在12周时的疗效始终更优;这一结果在两项研究的24周时均具有统计学意义,在一项研究中持续到52周。恶心是临床试验中报告的常见不良事件,但导致停药的情况很少。其靶向作用机制、卓越的疗效和良好的耐受性使伐尼克兰成为戒烟治疗选择中受欢迎且有用的补充药物。