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一项关于伐尼克兰与安非他酮联合用于戒烟的随机对照试验:一线使用的临床意义

An RCT with the combination of varenicline and bupropion for smoking cessation: clinical implications for front line use.

作者信息

Cinciripini Paul M, Minnix Jennifer A, Green Charles E, Robinson Jason D, Engelmann Jeffrey M, Versace Francesco, Wetter David W, Shete Sanjay, Karam-Hage Maher

机构信息

Department of Behavioral Science, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Department of Pediatrics, Center for Clinical Research and Evidence-Based Medicine, The University of Texas at Houston Health Sciences Center, Houston, TX, USA.

出版信息

Addiction. 2018 Apr 21. doi: 10.1111/add.14250.

Abstract

BACKGROUND AND AIMS

Despite the availability of several efficacious smoking cessation treatments, fewer than 25% of smokers who quit remain abstinent 1 year post-treatment. This study aimed to determine if varenicline and bupropion combination treatment would result in higher abstinence rates than varenicline alone.

DESIGN

A double-blind, randomized, parallel-group smoking cessation clinical trial in which participants were exposed to 12 weeks of treatment and followed for 12 months.

SETTING

Hospital-based out-patient clinic in Texas, USA specializing in cancer prevention.

PARTICIPANTS

A total of 385 community smokers (58.44% male) who smoked 1 pack of cigarettes/day [mean = 19.66 cigarettes/day, standard deviation (SD) = 9.45]; had average carbon monoxide (CO) of 26.43 parts per million (SD = 13.74); and were moderately dependent (Fagerström Test for Cigarette Dependence = 4.79; SD = 2.07).

INTERVENTIONS AND COMPARATOR

Smokers were randomized in a 3 : 1 (active: Placebo) ratio to 12 weeks of treatment as follows: placebo (n = 56), varenicline (Var; n = 166), and varenicline + bupropion (Combo; n = 163).

MEASUREMENTS

A priori primary outcome: prolonged abstinence at 12 months.

SECONDARY OUTCOMES

7-day point prevalence abstinence and continuous abstinence; all abstinence measures at end of treatment and 6-month follow-ups.

FINDINGS

Intention-to-treat analysis: the Combo group (n = 163) failed to demonstrate superiority to the Var group (n = 166) for prolonged abstinence at 12 months [odds ratio (OR) = 0.91, 95% confidence interval (CI) = 0.50-1.64], supported by Bayes factor = 0.06. Both the Var (OR = 6.66, 95% CI = 1.61-59.27) and Combo groups (OR = 6.06, 95% CI = 1.45-54.09) demonstrated superiority to the Placebo group (n = 56; score = 8.38, P < 0.016).

CONCLUSIONS

The addition of bupropion to varenicline treatment does not appear to increase smoking abstinence rates above that of varenicline alone. The findings support previous research showing a consistently favorable effect of both varenicline and the combination of varenicline and bupropion on smoking cessation compared with placebo.

摘要

背景与目的

尽管有多种有效的戒烟治疗方法,但戒烟的吸烟者中不到25%在治疗后1年仍保持戒烟状态。本研究旨在确定伐尼克兰和安非他酮联合治疗是否比单独使用伐尼克兰能带来更高的戒烟率。

设计

一项双盲、随机、平行组戒烟临床试验,参与者接受12周治疗并随访12个月。

地点

美国得克萨斯州一家专门从事癌症预防的医院门诊。

参与者

共有385名社区吸烟者(男性占58.44%),每天吸烟1包[平均=每天19.66支香烟,标准差(SD)=9.45];平均一氧化碳(CO)含量为百万分之26.43(SD=13.74);且为中度依赖(香烟依赖的法格斯特龙测试=4.79;SD=2.07)。

干预措施与对照

吸烟者按3:1(活性药物:安慰剂)的比例随机分配接受12周治疗,具体如下:安慰剂组(n=56)、伐尼克兰组(Var;n=166)和伐尼克兰+安非他酮组(联合组;n=163)。

测量指标

预先设定的主要结局:12个月时的长期戒烟。

次要结局

7天点患病率戒烟和持续戒烟;治疗结束时及6个月随访时的所有戒烟指标。

研究结果

意向性分析:联合组(n=163)在12个月时的长期戒烟方面未显示出优于伐尼克兰组(n=【此处原文有误,应为166】)[优势比(OR)=0.91,95%置信区间(CI)=0.50 - 1.64],贝叶斯因子=0.06支持该结果。伐尼克兰组(OR=6.66,95%CI=1.61 - 59.27)和联合组(OR=6.06,95%CI=1.45 - 54.09)均显示出优于安慰剂组(n=56;得分=8.38,P<0.016)。

结论

在伐尼克兰治疗中添加安非他酮似乎并未使戒烟率高于单独使用伐尼克兰。这些发现支持了先前的研究,即与安慰剂相比,伐尼克兰以及伐尼克兰与安非他酮联合使用在戒烟方面始终具有良好效果。

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