Scenarios for the long‐term efficacy of amyloid‐targeting therapies in the context of the natural history of Alzheimer's disease

Author:

Raket Lars Lau12ORCID,Cummings Jeffrey3,Moscoso Alexis4,Villain Nicolas56,Schöll Michael478

Affiliation:

1. Eli Lilly and Company Indianapolis Indiana USA

2. Clinical Memory Research Unit Department of Clinical Sciences Lund University Lund Sweden

3. Chambers‐Grundy Center for Transformative Neuroscience Pam Quirk Brain Health and Biomarker Laboratory Department of Brain Health School of Integrated Health Sciences University of Nevada Las Vegas (UNLV) Las Vegas Nevada USA

4. Wallenberg Centre for Molecular and Translational Medicine and the Department of Psychiatry and Neurochemistry University of Gothenburg Huvudbyggnad Vasaparken, Universitetsplatsen 1 Gothenburg Sweden

5. Department of Neurology Institute of Memory and Alzheimer's Disease AP‐HP Sorbonne Université Pitié‐Salpêtrière Hospital Paris France

6. Sorbonne Université INSERM U1127 Institut du Cerveau ‐ ICM Paris France

7. Department of Clinical Physiology Sahlgrenska University Hospital Gothenburg Sweden

8. Dementia Research Centre Queen Square Institute of Neurology University College London London UK

Abstract

AbstractINTRODUCTIONRecent clinical trials of amyloid beta (Aβ)‐targeting therapies in Alzheimer's disease (AD) have demonstrated a clinical benefit over 18 months, but their long‐term impact on disease trajectory is not yet understood. We propose a framework for evaluating realistic long‐term scenarios.METHODSResults from recent phase 3 trials of Aβ‐targeting antibodies were integrated with an estimate of the long‐term patient‐level natural history trajectory of the Clinical Dementia Rating‐Sum of Boxes (CDR‐SB) score to explore realistic long‐term efficacy scenarios.RESULTSThree distinct long‐term efficacy scenarios were examined, ranging from conservative to optimistic. These extrapolations of positive phase 3 trials suggested treatments delayed onset of severe dementia by 0.3 to 0.6 years (conservative), 1.1 to 1.9 years (intermediate), and 2.0 to 4.2 years (optimistic).DISCUSSIONOur study provides a common language for long‐term impact of disease‐modifying treatments. Our work calls for studies with longer follow‐up and results from early intervention trials to provide a comprehensive assessment of these therapies' true long‐term impact.Highlights We present long‐term scenarios of the efficacy of AD therapies. In this framework, scenarios are defined relative to the natural history of AD. Long‐term projections with different levels of optimism can be compared. It provides a common language for expressing beliefs about long‐term efficacy.

Publisher

Wiley

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