Wednesday, 2 April 2003

This presentation is part of : Poster Session 1

Cognition is Physicians’ Main Indicator of Treatment Efficacy in Alzheimer’s Disease Patients

S Hasselbalch1, H Hampel2, CJ Kalisvaart3, W Kozubski4, E Salmon5, H Tilker6, F Túry7, V Vagenas8, L Johansen9, Y Xu10, S Richardson11, N Kumar10, and P Johannsen12. (1) University Hospital, Copenhagen, Denmark, (2) Department of Psychiatry, Ludwig-Maximilian University, Munich, Germany, (3) Medisch Centrum Alkmaar, Alkmaar, Netherlands, (4) University School of Medicine, Poznan, Poland, (5) Domaine Universitaire Du Sart Tilman Angleur, Liège, Belgium, (6) Four Rivers Clinical Research Inc., Paducah, KY, USA, (7) Semmelweis University, Budapest, Hungary, (8) 1st IKA Hospital, Athens, Greece, (9) Pfizer Denmark, Ballerup, Denmark, (10) Pfizer Inc., New York, NY, USA, (11) Eisai Inc., Teaneck, NJ, USA, (12) Aarhus University Hospital, Aarhus, Denmark

Objective: To examine the domains influencing physicians’ judgment of clinical benefit in donepezil-treated Alzheimer’s disease (AD) patients, during the pre-randomization phase of the donepezil AWARE (Aricept WAshout and REchallenge) study.

Background: AD patients who do not exhibit improvement are often discontinued from cholinesterase inhibitor therapy. However, although therapeutic benefits may be apparent in several domains, such as cognition, behavior, and activities of daily living (ADL), there is currently no standard clinical approach to determine treatment success in AD patients.

Design: AWARE consists of 3 phases: 1) 24-week, pre-randomization, open-label donepezil treatment phase; 2) 12-week, randomized, double-blind, placebo-controlled phase; 3) 12-week, single-blind donepezil treatment phase. During the first, open-label phase, all patients received donepezil. During the subsequent, double-blind phase, patients were randomized to continue on donepezil treatment or switch to placebo. In the final, single-blind phase, donepezil-treated patients continued to receive donepezil, while placebo-treated patients were rechallenged with donepezil.

Materials and Methods: Patients with mild to moderate, possible or probable AD were enrolled in the pre-randomization phase. All patients received donepezil 5 mg/day for 28 days, then 10 mg/day. Clinical benefit was assessed at Weeks 12, 18, and 24. Patients showing "observed clinical benefit" improved from baseline on the Mini-Mental State Examination (MMSE) or the physician was sufficiently certain of clinical benefit to warrant continued treatment (assessed by formal questionnaire). Physicians indicated which domains (cognition, ADL, behavior, caregiver request, other) most influenced their decision. Patients showing “no apparent clinical benefit” were randomized to receive either donepezil or placebo in the second, double-blind phase of AWARE. These double-blind data will be the subject of further presentations.

Results: Clinical benefit was classified in 619 of the 817 enrolled patients. The majority (68%) of physicians’ decisions were based upon cognition, whereas other domains were less influential (ADL, 14% of decisions; behavior, 11%; caregiver request, 6%; other, 1%). 417 patients showed “observed clinical benefit” (MMSE mean change from baseline, 2.3), and physicians were sufficiently certain of benefit to warrant continued therapy in 400 of these.

Conclusion: In the majority of patients, cognition was the most influential domain in physicians’ decisions regarding clinical benefit. There was strong agreement between physician global rating of the patient and the MMSE, supporting the observation that cognition was the main indicator used to assess clinical benefit.

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