TREATMENT PREFERENCES FOR PHARMACOLOGICAL THERAPIES IN ALZHEIMER'S DISEASE: A SCOPING REVIEW OF STATED-PREFERENCE STUDIES

Author(s)

GaHee Choi, Bachelor's degree1, Yebin Yoon, PharmD2, EUI-KYUNG LEE, PhD1, Mi-Hai Park, PhD1, Ha-Jun Song, PharmD1, Sun-Kyeong Park, PhD2.
1Sungkyunkwan University, Suwon, Korea, Republic of, 2The Catholic University of Korea, Bucheon, Korea, Republic of.
OBJECTIVES: Alzheimer’s disease (AD) treatments involve complex trade-offs among clinical efficacy, safety, and treatment burden. This scoping review aimed to identify and map stated-preference evidence on treatment attributes and preferences for pharmacological therapies in AD.
METHODS: PubMed and Cochrane Library were searched for stated-preference studies evaluating AD pharmacological or disease-modifying therapy (DMT). Eligible studies used conjoint-based or stated-choice methods and included patients or individuals with cognitive concerns, caregivers, older adults, or clinical stakeholders. Reviews, protocols, non-pharmacological care, and diagnostic preference studies were excluded. Data were charted on study characteristics, respondent population, treatment scenario, elicitation method, attributes, and findings.
RESULTS: Of 400 identified records, four met the inclusion criteria. Respondents comprised general older adults, adults with AD-related risk or mild cognitive concerns, caregivers, and neurologists; no study directly elicited stated-choice preferences from patients with moderate or severe AD. All studies used hypothetical stated-choice tasks; three were discrete choice experiments. Choice contexts ranged from broad DMT concepts and symptom-onset or cognitive-decline delay to a more therapy-specific amyloid plaque-lowering profile. Efficacy was framed as time-related benefits, including delayed onset/progression, longer normal-memory time, and slowed cognitive decline. Safety attributes reflected the treatment concept: broader DMT-oriented studies included severe outcomes such as stroke, death, or permanent disability, whereas the amyloid-targeted profile included ARIA-E/brain swelling, nausea, and treatment-related adverse events. Across studies, delaying progression/onset and serious safety risks were frequently evaluated. Where caregivers and neurologists were compared, both prioritized clinical benefit and ARIA-E risk, while neurologists emphasized administration route and frequency and caregivers were more sensitive to treatment titration.
CONCLUSIONS: Stated-preference evidence for AD pharmacotherapies remains sparse, with substantial variation in treatment contexts, attributes, and respondent groups. Future studies should use therapy-specific treatment profiles and respondent groups that reflect the clinical population and decision context of the therapies being evaluated.

Conference/Value in Health Info

2026-11, ISPOR Europe 2026, Vienna, Austria

Value in Health, Volume 29, Issue 12S

Code

PCR176

Topic

Patient-Centered Research

Disease

Neurological Disorders, No Additional Disease & Conditions/Specialized Treatment Areas

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