伐尼克兰
胞苷
医学
戒烟
随机对照试验
中止
禁欲
尼古丁替代疗法
安慰剂
物理疗法
内科学
精神科
替代医学
烟碱激动剂
病理
受体
作者
RJ Courtney,Hayden McRobbie,Piotr Tutka,NA Weaver,C M Mendelsohn,Anthony Shakeshaft,Saki Rubaiya Talukder,Christopher J. MacDonald,Dennis Thomas,Bch Kwan,Neil J. Walker,Coral Gartner,RP Mattick,C. Paul,SG Ferguson,NA Zwar,RL Richmond,CM Doran,V. Boland,Wendy L. Hall,Robert West,M. Farrell
出处
期刊:JAMA network open
[American Medical Association]
日期:2021-01-01
卷期号:326 (1): 56-64
被引量:5
摘要
IMPORTANCE: Cytisine is more effective than placebo and nicotine replacement therapy for
smoking cessation. However, cytisine has not been tested against the most effective smoking
cessation medication, varenicline, which is associated with adverse events known to lead to
discontinuation of therapy. OBJECTIVE: To examine whether standard cytisine treatment (25 days) was at least as
effective as standard varenicline treatment (84 days) for smoking cessation. DESIGN, SETTING, AND PARTICIPANTS: This noninferiority, open-label randomized clinical trial
with allocation concealment and blinded outcome assessment was undertaken in Australia
from November 2017 through May 2019; follow-up was completed in January 2020. A total
of 1452 Australian adult daily smokers willing to make a quit attempt were included. Data
collection was conducted primarily by computer-assisted telephone interview, but there was
an in-person visit to validate the primary outcome. INTERVENTIONS: Treatments were provided in accordance with the manufacturers’
recommended dosage: cytisine (n = 725), 1.5-mg capsules taken 6 times daily initially then
gradually reduced over the 25-day course; varenicline (n = 727), 0.5-mg tablets titrated to
1 mg twice daily for 84 days (12 weeks). All participants were offered referral to standard
telephone behavioral support. MAIN OUTCOMES AND MEASURES: The primary outcome was 6-month continuous abstinence
verified using a carbon monoxide breath test at 7-month follow-up. The noninferiority margin
was set at 5% and the 1-sided significance threshold was set at .025. RESULTS: Among 1452 participants who were randomized (mean [SD] age, 42.9 [12.7] years;
742 [51.1%] women), 1108 (76.3%) completed the trial. Verified 6-month continuous
abstinence rates were 11.7% for the cytisine group and 13.3% for the varenicline group (risk
difference, −1.62% [1-sided 97.5% CI, −5.02% to ]; P = .03 for noninferiority). Self-reported
adverse events occurred less frequently in the cytisine group (997 events among 482
participants) compared with the varenicline group (1206 events among 510 participants) and
the incident rate ratio was 0.88 (95% CI, 0.81 to 0.95; P = .002). CONCLUSIONS AND RELEVANCE: Among daily smokers willing to quit, cytisine treatment for 25
days, compared with varenicline treatment for 84 days, failed to demonstrate noninferiority
regarding smoking cessation.
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