Effect of Cytisine vs Varenicline on Smoking Cessation: A Randomized Clinical Trial.


Journal

JAMA
ISSN: 1538-3598
Titre abrégé: JAMA
Pays: United States
ID NLM: 7501160

Informations de publication

Date de publication:
06 07 2021
Historique:
entrez: 6 7 2021
pubmed: 7 7 2021
medline: 14 7 2021
Statut: ppublish

Résumé

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. To examine whether standard cytisine treatment (25 days) was at least as effective as standard varenicline treatment (84 days) for smoking cessation. 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. 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. 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. 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). 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. anzctr.org.au Identifier: ACTRN12616001654448.

Identifiants

pubmed: 34228066
pii: 2781643
doi: 10.1001/jama.2021.7621
pmc: PMC8261608
doi:

Substances chimiques

Alkaloids 0
Azocines 0
Quinolizines 0
Smoking Cessation Agents 0
cytisine 53S5U404NU
Varenicline W6HS99O8ZO

Types de publication

Comparative Study Equivalence Trial Journal Article Multicenter Study Randomized Controlled Trial Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

56-64

Subventions

Organisme : NIAID NIH HHS
ID : R01 AI083188
Pays : United States

Commentaires et corrections

Type : CommentIn

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Auteurs

Ryan J Courtney (RJ)

National Drug and Alcohol Research Centre, University of New South Wales, Sydney, Australia.

Hayden McRobbie (H)

National Drug and Alcohol Research Centre, University of New South Wales, Sydney, Australia.

Piotr Tutka (P)

Department of Experimental and Clinical Pharmacology, University of Rzeszow, Rzeszow, Poland.

Natasha A Weaver (NA)

School of Medicine and Public Health, University of Newcastle, Newcastle, Australia.

Dennis Petrie (D)

Centre for Health Economics, Monash Business School, Monash University, Clayton, Australia.

Anthony Shakeshaft (A)

National Drug and Alcohol Research Centre, University of New South Wales, Sydney, Australia.

Saki Talukder (S)

National Drug and Alcohol Research Centre, University of New South Wales, Sydney, Australia.

Christel Macdonald (C)

National Drug and Alcohol Research Centre, University of New South Wales, Sydney, Australia.

Dennis Thomas (D)

Priority Research Centre for Healthy Lungs, Hunter Medical Research Institute, University of Newcastle, Newcastle, Australia.

Benjamin C H Kwan (BCH)

St George and Sutherland Clinical School, University of New South Wales, Sydney, Australia.

Natalie Walker (N)

National Institute for Health Innovation, School of Population Health, University of Auckland, Auckland, New Zealand.

Coral Gartner (C)

School of Public Health, University of Queensland, Herston, Australia.

Richard P Mattick (RP)

National Drug and Alcohol Research Centre, University of New South Wales, Sydney, Australia.

Christine Paul (C)

School of Medicine and Public Health, University of Newcastle, Newcastle, Australia.

Stuart G Ferguson (SG)

Tasmanian School of Medicine, College of Health and Medicine, University of Tasmania, Hobart, Australia.

Nicholas A Zwar (NA)

Faculty of Health Sciences and Medicine, Bond University, Robina, Australia.

Robyn L Richmond (RL)

School of Population Health, University of New South Wales, Sydney, Australia.

Christopher M Doran (CM)

Cluster for Resilience and Wellbeing, Appleton Institute, Central Queensland University, Brisbane, Australia.

Veronica C Boland (VC)

National Drug and Alcohol Research Centre, University of New South Wales, Sydney, Australia.

Wayne Hall (W)

National Centre for Youth Substance Use Research, University of Queensland, Herston, Australia.

Robert West (R)

Department of Behavioural Science and Health, University College London, London, England.

Michael Farrell (M)

National Drug and Alcohol Research Centre, University of New South Wales, Sydney, Australia.

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Classifications MeSH