Use of varenicline for 4 weeks before quitting smoking: decrease in ad lib smoking and increase in smoking cessation rates

Arch Intern Med. 2011 Apr 25;171(8):770-7. doi: 10.1001/archinternmed.2011.138.

Abstract

Background: The use of varenicline tartrate alleviates postquit withdrawal discomfort, but it also seems to reduce the "reward" associated with smoking. The current treatment schedule, which commences 1 week before quitting, relies primarily on the first mechanism. We set out to determine whether increasing the prequit medication period renders cigarettes less satisfying and facilitates quitting.

Methods: One hundred one smokers attending a stop-smoking clinic in London, United Kingdom, were randomly allocated to receive varenicline for 4 weeks before the target quit date (TQD) or to receive placebo for 3 weeks before the TQD, followed by varenicline for 1 week before the TQD. In both groups, standard varenicline treatment was given for 3 months after the TQD. Measures included smoking satisfaction and smoke intake before quitting, urges to smoke and withdrawal discomfort after quitting, and sustained abstinence from the TQD to 3 months.

Results: Varenicline preloading reduced prequit enjoyment of smoking (P = .004) and smoke intake (P < .001), with 36.7% of participants reducing their cotinine concentrations by more than 50% (reducers). Varenicline preloading did not affect postquit withdrawal symptoms, but it increased 12-week abstinence rates (47.2% in the varenicline arm vs 20.8% in the placebo arm, P = .005). The effect was particularly strong among the reducers in the varenicline arm (66.7% in reducers vs 22.6% in nonreducers, P = .002). Varenicline preloading was well tolerated.

Conclusions: Although several issues remain to be clarified, varenicline preloading can generate a substantial reduction in ad lib smoking and enhance 12-week quit rates. Current treatment schedules may lead to suboptimal treatment results. Trials with longer follow-up periods are needed to corroborate these findings. Trial Registration clinicaltrials.gov Identifier: NCT00789074.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Benzazepines / administration & dosage
  • Benzazepines / pharmacology
  • Benzazepines / therapeutic use*
  • Biomarkers / blood
  • Cotinine / blood
  • Double-Blind Method
  • Drug Administration Schedule
  • Female
  • Humans
  • London
  • Male
  • Middle Aged
  • Nicotinic Agonists / administration & dosage
  • Nicotinic Agonists / pharmacology
  • Nicotinic Agonists / therapeutic use*
  • Quinoxalines / administration & dosage
  • Quinoxalines / pharmacology
  • Quinoxalines / therapeutic use*
  • Receptors, Nicotinic / drug effects
  • Smoking Cessation / methods*
  • Smoking Prevention*
  • Substance Withdrawal Syndrome / drug therapy*
  • Time Factors
  • Treatment Outcome
  • Varenicline

Substances

  • Benzazepines
  • Biomarkers
  • Nicotinic Agonists
  • Quinoxalines
  • Receptors, Nicotinic
  • Cotinine
  • Varenicline

Associated data

  • ClinicalTrials.gov/NCT00789074