Donanemab: Appropriate use recommendations
Donanemab (Kisunla®), an IgG1 monoclonal antibody targeting N-terminal pyroglutamate-modified forms of amyloid-β, is approved in the United States for treatment of early symptomatic Alzheimer's disease (AD). Appropriate Use Recommendations (AUR) were developed to guide the implementation of donanemab in real-world practice, prioritizing safety considerations and opportunity for effectiveness. The AUR were developed by the AD and Related Disorders Therapeutic Workgroup by consensus, integrating available data and expert opinion. Appropriate candidates for donanemab treatment include persons with mild cognitive impairment or mild dementia due to AD (Clinical Stages 3-4, MMSE 20-30) who have biomarker confirmation of AD pathology by PET or CSF. Tau PET is not required for eligibility. Apolipoprotein E (APOE) genotyping should be performed prior to treatment to inform an individual's risk of developing Amyloid-Related Imaging Abnormalities (ARIA). Pre-treatment MRI should be obtained no more than 12 months prior to treatment. Patients with findings of >4 cerebral microbleeds, cortical superficial siderosis or a major vascular contribution to cognitive impairment should be excluded from treatment. The decision to initiate therapy should be grounded in a shared decision-making process that emphasizes the patient's values and goals of care. Donanemab is administered as a monthly intravenous infusion. Surveillance MRIs to evaluate for ARIA should be performed prior to the 2nd, 3rd, 4th and 7th infusions, prior to the 12th dose in higher risk individuals, and at any time ARIA is suspected clinically. Clinicians may consider discontinuing treatment if amyloid clearance is demonstrated by amyloid PET, typically obtained 12-18 months after initiating treatment.
Authors
- Alireza Atri (ORCID: https://orcid.org/0000-0003-4405-6973)
- Suzanne Hendrix (ORCID: https://orcid.org/0000-0002-2374-7727)
- G D Rabinovici
- Liana G. Apostolova (ORCID: https://orcid.org/0000-0003-1823-2451)
- Paul S. S Aisen (ORCID: https://orcid.org/0000-0002-2896-5838)
- R.C. Petersen
- Myron Weiner
- Steven Mark Greenberg (ORCID: https://orcid.org/0000-0003-1792-8887)
- Suzanne E. Schindler (ORCID: https://orcid.org/0000-0002-1680-1465)
- D. J. Selkoe
- Steve Salloway
- Jeffrey L. Cummings
Institutions
- University of Southern California (US)
- Brigham and Women's Hospital (US)
- University of Nevada, Las Vegas (US)
- Harvard University (US)
- University of California, San Francisco (US)
- Washington University in St. Louis (US)
- Butler Hospital (US)
- Banner Health (US)
- Massachusetts General Hospital (US)
- University Memory and Aging Center (US)
- Treatment Research Institute (US)
- Mayo Clinic in Arizona (US)
- Banner Sun Health Research Institute (US)
- TetraLogic Pharmaceuticals (United States) (US)
- Indiana University School of Medicine
- Indiana University – Purdue University Indianapolis (US)
Publication Details
- Journal
- The Journal of Prevention of Alzheimer s Disease
- Published
- 2025-03-30
- DOI
- https://doi.org/10.1016/j.tjpad.2025.100150
- Citations
- 111
- Primary Topic
- Dementia and Cognitive Impairment Research
- Type
- article
- Field-Weighted Citation Impact
- 163.31
Funders
- Bristol-Myers Squibb
- Alzheimer's Drug Discovery Foundation
- Eli Lilly and Company
- Biogen
- Alnylam Pharmaceuticals
- Sunovion
- Prothena
- University of Oxford
- Eisai
- Novo Nordisk
- H. Lundbeck A/S
- Grifols
- Genentech
- Allergan
- Avid Radiopharmaceuticals
- National Institute on Aging
- National Institute of General Medical Sciences
- National Institute of Neurological Disorders and Stroke