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Effects of the active amyloid beta immunotherapy CAD106 on PET measurements of amyloid plaque deposition in cognitively unimpaired APOE ε4 homozygotes

Riviere Marie-Emmanuelle; Langbaum Jessica B.; Turner R. Scott; Rinne Juha O.; Sui Yihan; Cazorla Pilar; Ricart Javier; Meneses Kathleen; Caputo Angelika; Tariot Pierre N.; Reiman Eric M.; Graf Ana

Effects of the active amyloid beta immunotherapy CAD106 on PET measurements of amyloid plaque deposition in cognitively unimpaired APOE ε4 homozygotes

Riviere Marie-Emmanuelle
Langbaum Jessica B.
Turner R. Scott
Rinne Juha O.
Sui Yihan
Cazorla Pilar
Ricart Javier
Meneses Kathleen
Caputo Angelika
Tariot Pierre N.
Reiman Eric M.
Graf Ana
Katso/Avaa
Alzheimer s Dementia - 2023 - Riviere - Effects of the active amyloid beta immunotherapy CAD106 on PET measurements of.pdf (561.8Kb)
Lataukset: 

Wiley
doi:10.1002/alz.13532
URI
https://alz-journals.onlinelibrary.wiley.com/doi/abs/10.1002/alz.13532
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Julkaisun pysyvä osoite on:
https://urn.fi/URN:NBN:fi-fe2025082791132
Tiivistelmä

Introduction: Alzheimer's Prevention Initiative Generation Study 1 evaluated amyloid beta (Aβ) active immunotherapy (vaccine) CAD106 and BACE-1 inhibitor umibecestat in cognitively unimpaired 60- to 75-year-old participants at genetic risk for Alzheimer's disease (AD). The study was reduced in size and terminated early. Results from the CAD106 cohort are presented.

Methods: Sixty-five apolipoprotein E ε4 homozygotes with/without amyloid deposition received intramuscular CAD106 450 μg (n = 42) or placebo (n = 23) at baseline; Weeks 1, 7, 13; and quarterly; 51 of them had follow-up Aβ positron emission tomography (PET) scans at 18 to 24 months.

Results: CAD106 induced measurable serum Aβ immunoglobulin G titers in 41/42 participants, slower rates of Aβ plaque accumulation (mean [standard deviation] annualized change from baseline in amyloid PET Centiloid: -0.91[5.65] for CAD106 versus 8.36 [6.68] for placebo; P < 0.001), and three amyloid-related imaging abnormality cases (one symptomatic).

Discussion: Despite early termination, these findings support the potential value of conducting larger prevention trials of Aβ active immunotherapies in individuals at risk for AD.

Highlights: This was the first amyloid-lowering prevention trial in persons at genetic risk of late-onset Alzheimer's disease (AD). Active immunotherapy targeting amyloid (CAD106) was tested in this prevention trial. CAD106 significantly slowed down amyloid plaque deposition in apolipoprotein E homozygotes. CAD106 was generally safe and well tolerated, with only three amyloid-related imaging abnormality cases (one symptomatic). Such an approach deserves further evaluation in larger AD prevention trials.

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