This meta-analysis pooled thirty-seven real-world studies of lecanemab, covering ARIA, discontinuation, cognition and amyloid PET. Any ARIA was 15.1%, ARIA-E 6.5%, ARIA-H 11.5% and symptomatic ARIA 1.3%, with US rates above Asian rates. ARIA rose with APOE e4 dose, from 11.0% in non-carriers to 34.1% in homozygotes, and with baseline microhaemorrhage. Total discontinuation was 12.2%, ARIA-related discontinuation 3.5%, infusion-related reactions 18.5% and serious adverse events 2.8%. Amyloid PET fell at 6 months (-28.5 Centiloid) and 12 months (SUVR -0.171), while cognitive measures showed no significant change. The pooled cohorts had no control groups, so the authors state that efficacy cannot be inferred.
Why it is interesting: The review gives ARIA incidence in routine practice, stratified by APOE genotype and baseline microbleeds. Amyloid reduction is recorded, but the uncontrolled design leaves any cognitive effect unresolved.
Cite this item
BibTeX
Free sign-up. A digest of the new papers twice a week, grouped by domain.