Data di Pubblicazione:
2023
Abstract:
After the CLARITY-AD clinical trial results of lecanemab were interpreted as positive, and supporting the amyloid hypothesis, the drug received accelerated Food and Drug Administration approval. However, we argue that benefits of lecanemab treatment are uncertain and may yield net harm for some patients, and that the data do not support the amyloid hypothesis. We note potential biases from inclusion, unblinding, dropouts, and other issues. Given substantial adverse effects and subgroup heterogeneity, we conclude that lecanemab's efficacy is not clinically meaningful, consistent with numerous analyses suggesting that amyloid-beta and its derivatives are not the main causative agents of Alzheimer's disease dementia.
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
Alzheimer’s disease; amyloid-β; antibody; lecanemab; subgroup analysis
Elenco autori:
Kepp, Kasper P; Sensi, Stefano L; Johnsen, Kasper B; Barrio, Jorge R; Høilund-Carlsen, Poul F; Neve, Rachael L; Alavi, Abass; Herrup, Karl; Perry, George; Robakis, Nikolaos K; Vissel, Bryce; Espay, Alberto J
Link alla scheda completa:
Pubblicato in: