2021
DOI: 10.1002/alz.12379
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Bayes analysis supports null hypothesis of anti‐amyloid beta therapy in Alzheimer's disease

Abstract: Numerous clinical trials of anti-amyloid beta (Aβ) immunotherapy in Alzheimer's disease have been performed. None of these have provided convincing evidence for beneficial effects. Using traditional frequentist meta-analysis, the conclusion is that there is absence of evidence for a therapeutic effect, with a point estimate effect size of 0.05 (95% confidence interval −0.00 to 0.10, P = .055). In addition, this non-significant effect equates to 0.4 points per year on the cognitive subscale of the Alzheimer's D… Show more

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Cited by 38 publications
(36 citation statements)
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References 14 publications
(27 reference statements)
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“…A recent meta-analysis showed that amyloid removal does not lead to clinical improvement 14. Several trials have revealed that treatment with anti-amyloid therapies does not result in clinical benefits, and even if a future RCT reports positive results, it cannot be interpreted without accounting for all the previous neutral results 15…”
Section: An Unusual Approval Processmentioning
confidence: 99%
“…A recent meta-analysis showed that amyloid removal does not lead to clinical improvement 14. Several trials have revealed that treatment with anti-amyloid therapies does not result in clinical benefits, and even if a future RCT reports positive results, it cannot be interpreted without accounting for all the previous neutral results 15…”
Section: An Unusual Approval Processmentioning
confidence: 99%
“…First, Richard et al.’s meta‐analytic work compared the conclusions that can be drawn from the systematic review of phase 3 anti‐amyloid trials in AD using a frequentist approach with the conclusions from a Bayesian framework 14 . The conclusion from the frequentist analysis was “One cannot reject the assumption of the absence of an effect.” This information leaves the question “Is there evidence for a beneficial effect of anti‐amyloid treatment based on the published phase 3 trials so far?” unanswered.…”
Section: The Bayesian Framework Explainedmentioning
confidence: 99%
“…On June 7, 2021, Food and Drug Administration (FDA) approved Aduhelm (aducanumab) [67], a human IgG1 anti-Aβ monoclonal antibody claiming to reduce, in a dose-and time dependent manner, β-amyloid plaques in AD patients, as assessed by Positron Emission Tomography (PET) studies [68]. Despite the reduction of Aβ-burden could provide a surrogate endpoint to predict a meaningful therapeutic benefit, clinical data failed to show a significant protection from cognitive and functional decline over considerable adverse events, leaving significant uncertainty about an acceptable risk/benefit profile of the drug [69]. Furthermore, a nine-year post-approval confirmatory study was committed in order to attempt a reassessment of the real efficacy of the treatment, also in view of its burdensome costs.…”
Section: Figurementioning
confidence: 99%