Patient journey and decision processes for anti-amyloid therapy in Alzheimer's disease
- PMID: 40237866
- PMCID: PMC12003442
- DOI: 10.1007/s00415-025-13059-3
Patient journey and decision processes for anti-amyloid therapy in Alzheimer's disease
Abstract
Introduction: We utilized the Veterans Affairs Healthcare System administrative database to study the clinical decision-making processes for anti-amyloid therapy (AAT).
Methods: Patients with clinical notes mentioning lecanemab were identified (March 2023-June 2024) for manual review and structured database queries.
Results: From an initial sample (N = 2499), 1064 patients (55,000 notes) were reviewed manually (mean age 76 years; 7.3% women; 9.2% Black; 3.9% Hispanic). The AAT group (n = 56) had lower rates of common comorbidities, except post-traumatic stress disorder, than patients excluded from AAT (n = 528). The documented notes including "Lack of patient interest/resource constraints" (24.6% vs 3.6%), "anticoagulant use" (23.1% vs 10.7%), and "advanced AD" (18.6% vs 0), supplied partial explanations on exclusion vs inclusion.
Discussion: Only 5.3% of patients reached the point of care of being a candidate, scheduled for, or receiving AAT infusion. Patient preference and clinician discretion, especially regarding modifiable factors (e.g., medication regimens), appreciably influence the patient journey to AAT.
Keywords: Alzheimer’s disease; Anti-amyloid therapy; Electronic health records; Lecanemab; Mild cognitive impairment.
© 2025. This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply.
Conflict of interest statement
Declarations. Conflicts of interest: Amir Abbas Tahami Monfared, Michael Irizzary, and Quanwu Zhang are employees of Eisai Inc. The other authors declare no conflict of interest. Informed consent: All clinical notes from the nationwide VAHS database electronic health records (EHR) were searched, and the study was approved by the Bedford VA Healthcare System Institutional Review Board (IRB). Consent was not required for database analysis.
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References
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- Food and Drug Administration (2021) FDA grants accelerated approval for Alzheimer’s drug. https://www.fda.gov/news-events/press-announcements/fda-grants-accelerat..., Accessed on March 26, 2024
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- Food and Drug Administration (2023) FDA grants accelerated approval for Alzheimer’s disease treatment. https://www.fda.gov/news-events/press-announcements/fda-grants-accelerat..., Accessed on March 26, 2024
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