Evidence mapPaperPMID 41569381Full record

ArticleClinical drug investigation2026

Discrete Choice Experiment (DCE) as a Tool to Elicit Patient Preferences in a Complex Benefit-Risk Evaluation: A Case Study.

Jian-Yu E, Shahrul Mt-Isa, Kimberley Hockley, Kexin Zhu, Stephanie Tcherny-Lessenot, Juhaeri Juhaeri

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Article in Clinical drug investigation, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Jian-Yu EEpidemiology & Benefit-Risk Evaluation, Sanofi, Cambridge, MA, USA. Jian-Yu.E@sanofi.com.
Shahrul Mt-IsaMSD, Zurich, Switzerland.
Kimberley HockleyBristol Myers Squibb, London, UK.
Kexin ZhuEpidemiology & Benefit-Risk Evaluation, Sanofi, Morristown, NJ, USA.
Stephanie Tcherny-LessenotEpidemiology & Benefit-Risk Evaluation, Sanofi, Paris, France.
Juhaeri JuhaeriEpidemiology & Benefit-Risk Evaluation, Sanofi, Morristown, NJ, USA.

Funding

Innovative Medicines Initiative Joint Undertaking 115004
6 · The paper itself

Abstract

BACKGROUND AND

objectivesDiscrete choice experiment (DCE) is increasingly recognized for its utility to elicit patient preferences in benefit-risk (BR) evaluation, particularly when options entail complex tradeoffs. This rimonabant case study focused on the methodology and versatility of DCE to elicit patient preferences for anti-obesity drugs. This study aimed to demonstrate the application of DCE as a tool to capture patient preferences concerning the BR profile of rimonabant, focusing on attribute-based choices, preference elicitation, experimental design, quantitative analysis, and practical application.

methodsA DCE was conducted involving standard steps: identifying attributes and levels, constructing choice sets, designing the questionnaire, and analyzing responses. Two benefit and three risk attributes important to the BR profile of anti-obesity drugs were selected based on their significance to patients from published literature. Responses were analyzed using probit regression to quantify the preference for each attribute. Preference weights, derived from DCE, were combined with efficacy and safety data from clinical trials to estimate the utility function and probability of treatment selection. Lastly, the generated marginal rates of substitution (MRS) were used to present the extent to which patients were willing to trade off benefits to avoid risks.

resultsThe coefficients from the probit model indicated that psychiatric conditions (i.e., mild anxiety to severe depression) significantly impacted treatment preference, followed by cardiovascular conditions, weight loss, and gastrointestinal conditions. On average, rimonabant was preferred over placebo 67% of the time. On the basis of MRS, to avoid a 1% increase of psychiatric condition, patients would be willing to forgo a 3.9% reduction in number of people achieving 10% weight loss, or a 0.44 level of improvement in high-density lipoprotein cholesterol, which elucidates how patients value benefits and risks when deciding on a treatment.

conclusionsThis case study reaffirmed the utility of DCE as a valuable tool for BR evaluations, which aligned with what patients deemed important. The case study demonstrated essential attributes for anti-obesity medications. The methodological rigor and flexibility of DCE provided a robust framework for understanding, quantifying and analyzing preferences. The integration of elicited patient preferences, utility functions, and relevant clinical data offered quantitative insights into the structured BR assessment for regulatory decision-making and beyond.

Indexed as

Anti-Obesity AgentsChoice BehaviorPatient PreferenceHumansRimonabantRisk AssessmentSurveys and QuestionnairesAnti-Obesity AgentsRimonabant

Identifiers

PMID41569381
PMCPMC12950029

What Socratic holds

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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 Socratic graph.