Evidence map›Paper›PMID 28275830›Full record

Trial reportPsychopharmacology2017

Benefits of varenicline vs. bupropion for smoking cessation: a Bayesian analysis of the interaction of reward sensitivity and treatment.

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

Registry-linked trialOpen access · greenAbstract readComparative StudyRandomized Controlled Trial
In one paragraph

Trial report in Psychopharmacology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00507728 (Pharmacogenetics, Emotional Reactivity and Smoking), which is not on this map. Cited by 20 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 2 pooled it
1.2field-weighted citation impact, top 21% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT00507728 phase2 / phase3completednot on this map

Pharmacogenetics, Emotional Reactivity and Smoking

TypeinterventionalSponsorM.D. Anderson Cancer CenterRan2005 to 2019Enrolled646ConditionsTobacco Use Disorder, Smoking CessationArmsBupropion, Varenicline, Placebo, Smoking Cessation Counseling
3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 2 syntheses or guidelines pooled it, 24 citations in OpenAlex.

  1. Nicotine receptor partial agonists for smoking cessation.The Cochrane database of systematic reviews · 2023
    Pooled it
  2. Antidepressants for smoking cessation.The Cochrane database of systematic reviews · 2020
    Pooled it
  3. Trial
  4. Exenatide Adjunct to Nicotine Patch Facilitates Smoking Cessation and May Reduce Post-Cessation Weight Gain: A Pilot Randomized Controlled Trial.Nicotine & tobacco research : official journal of the Society for Research on Nicotine and Tobacco · 2021
    Trial
  5. Article
  6. Article
  7. Review
  8. Article
  9. Smoking cessation pharmacotherapy; varenicline or bupropion?Daru : journal of Faculty of Pharmacy, Tehran University of Medical Sciences · 2024
    Review
  10. Article
  11. Article
  12. Antidepressants for smoking cessation.The Cochrane database of systematic reviews · 2023
    Review
  13. Review
  14. Article
  15. Toward Precision Medicine for Smoking Cessation: Developing a Neuroimaging-Based Classification Algorithm to Identify Smokers at Higher Risk for Relapse.Nicotine & tobacco research : official journal of the Society for Research on Nicotine and Tobacco · 2020
    Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 1 country.

Paul M CinciripiniDepartment of Behavioral Science, The University of Texas MD Anderson Cancer Center, Unit 1330, PO Box 301439, Houston, TX, 77230-1439, USA. pcinciri@mdanderson.org.
Charles E GreenThe University of Texas at Houston Health Sciences Center, Houston, TX, USA.
Jason D RobinsonDepartment of Behavioral Science, The University of Texas MD Anderson Cancer Center, Unit 1330, PO Box 301439, Houston, TX, 77230-1439, USA.
Maher Karam-HageDepartment of Behavioral Science, The University of Texas MD Anderson Cancer Center, Unit 1330, PO Box 301439, Houston, TX, 77230-1439, USA.
Jeffrey M EngelmannDepartment of Behavioral Science, The University of Texas MD Anderson Cancer Center, Unit 1330, PO Box 301439, Houston, TX, 77230-1439, USA.
Jennifer A MinnixDepartment of Behavioral Science, The University of Texas MD Anderson Cancer Center, Unit 1330, PO Box 301439, Houston, TX, 77230-1439, USA.
David W WetterUniversity of Utah, Salt Lake City, UT, USA.
Francesco VersaceUniversity of Oklahoma Health Sciences Center and Oklahoma Tobacco Research Center, Oklahoma City, USA.
The University of Texas MD Anderson Cancer Center · USThe University of Texas Health Science Center at Houston · USUniversity of Oklahoma Health Sciences Center · USUniversity of Utah · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
UNIVERSITY OF TEXAS--SPORE IN LUNG CANCERP50CA070907 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI GIBBONS, DON LYNN · 1996 to 2024
$57.4M
Pharmacogenetics, Emotional Reactivity &Smoking(RMI)R01DA017073 · NIDA · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI CINCIRIPINI, PAUL MICHAEL · 2004 to 2009
$3.0M
Incentive salience and the neuropsychological underpinnings of cue-induced smoking relapseR01DA032581 · NIDA · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI VERSACE, FRANCESCO · 2012 to 2024
$2.5M
NCI NIH HHS P30 CA016672NCI NIH HHS P50 CA070907NIDA NIH HHS R01 DA017073NIDA NIH HHS R01 DA032581
6 · The paper itself

Abstract

rationaleWe have shown that differences in the level of neural activation to stimuli associated with smoking vs. natural rewards, a biomarker related to reward sensitivity, predict treatment outcome.

objectivesThis paper examined whether this biomarker moderates the impact of bupropion or varenicline on smoking cessation.

methodsPrior to treatment randomization, smokers (N = 180) in a placebo-controlled trial using bupropion and varenicline completed event-related potential recording (late positive potential, LPP) while viewing pleasant (P), cigarette (C)-related, and other pictures. We used Bayesian models to estimate the probability of interaction between treatment and the LPP for both efficacy and comparative effectiveness analyses.

resultsEfficacy analysis showed that smokers with more neural activation to pleasant vs. cigarette-related stimuli (P > C) had a 98-99% chance of achieving greater abstinence than placebo (OR >1.00), using either medication from the end of treatment (EOT, primary outcome) through the 3-month follow-up. Relative to placebo, smokers with higher activation to cigarette-related vs. pleasant stimuli (C > P) had a 99% chance of increased benefit from varenicline at both time points (OR >1), but only 67 and 43% with bupropion at the EOT and 3-month follow-up, respectively. Comparative effectiveness analysis found that smokers with the C > P activation pattern had a 95-98% chance of benefit from varenicline vs. bupropion, while P > C smokers had a 50-58% chance of similar improvement with varenicline at the EOT and 3 months.

conclusionsVarenicline appears to be the treatment of choice for smokers with the C > P pattern of neural activation, while for those showing P > C, varenicline and bupropion have similar efficacy.

Indexed as

RewardAdultAntidepressive Agents, Second-GenerationBayes TheoremBupropionFollow-Up StudiesHumansMiddle AgedNicotinic AgonistsSmoking CessationTobacco SmokingTreatment OutcomeVareniclineAntidepressive Agents, Second-GenerationBupropionNicotinic AgonistsVareniclineBayesian statisticsBupropionComparative effectivenessSmoking cessationVarenicline

Identifiers

PMID28275830
PMCPMC5901731
OpenAlexW2593773280

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.