The efficacy and safety of varenicline for smoking cessation using strategy in adult a flexible dosing smokers: a randomized controlled trial

被引:57
作者
Niaura, Raymond [1 ]
Hays, J. Taylor [2 ]
Jorenby, Douglas E. [3 ]
Leone, Frank T. [4 ]
Pappas, John E. [5 ]
Reeves, Karen R. [6 ]
Williams, Kathryn E. [6 ]
Billing, Clare B., Jr. [6 ]
机构
[1] Brown Univ, Providence, RI 02912 USA
[2] Mayo Clin, Coll Med, Rochester, MN USA
[3] Univ Wisconsin, Madison, WI USA
[4] Univ Penn, Philadelphia, PA 19104 USA
[5] Kentucky Med Res Ctr, Lexington, KY USA
[6] Pfizer Global Res & Dev, Groton, CT USA
关键词
D O I
10.1185/03007990802177523
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To determine whether self-regulated flexible dosing with varenicline tartrate is safe and effective for smoking cessation. Research design and methods: 320 healthy, motivated-to-quit smokers (>= 10 cigarettes/day) aged 18-65 years, entered a multicenter, randomized, double-blind, placebo-controlled study - conducted between December 26, 2001 and June 24, 2003 - with a 12-week treatment phase and 40-week, double-blind, non-treatment follow-up. Treatment consisted of varenicline or placebo in fixed doses (Week 1: titrated from 0.5 to 1.0 mg/day) followed by a self-regulated flexible schedule (Weeks 2-12: 0.5-2.0 mg/day). Main outcome measures: Primary outcomes included carbon monoxide-confirmed continuous abstinence rate (CAR) from smoking for Weeks 4 through 7, 9 through 12, and 9 through 52. Secondary outcomes included CAR from Weeks 9 through 24, 7-day point prevalence of abstinence, safety assessments, and measures of craving, withdrawal, and smoking reward. Results: Superior CARs were observed in varenicline-treated (n= 157) versus placebo participants (n= 155) for Weeks 4 through 7 (38.2 vs. 11.6%), 9 through 12 (40.1 vs. 11.6%), 9 through 24 (28.0 vs. 9.0%), and 9 through 52 (22.3 vs. 7.7%) (all p < 0.001). Seven-day point prevalence was higher in varenicline -treated than placebo participants at Weeks 12 (46.5 vs. 14.2%; p < 0.001), 24 (32.5 vs. 13.5%; p < 0.001), and 52 (28.0 vs. 13.5%; p = 0.001). Overall, medication compliance was high, although varenicline-treated, but not placebo, participants tended to taper down their dosage over time. Total treatment-emergent AEs were 77.1 % (varenicline: 121/157) and 65.8% (placebo: 102/155). Few AEs led to treatment discontinuation (varenicline: 11/157, 7.0% and placebo: 7/155, 4.5%). Participants were primarily healthy Caucasians, so more research is necessary to determine how applicable these findings are to other populations. Conclusions: A self-regulated, flexible dosing regimen of varenicline is well tolerated, with superior effectiveness versus placebo for smoking cessation.
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页码:1931 / 1941
页数:11
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