Memory and Aging Center, Department of Neurology, Weill Institute of Neuroscience, University of California, San Francisco, San Francisco, CA, USA.
Center for Alzheimer Research and Treatment, Department of Neurology, MassGeneral Brigham, Harvard Medical School, Boston, MA, USA.
Cell. 2023 Oct 26;186(22):4757-4772. doi: 10.1016/j.cell.2023.09.023. Epub 2023 Oct 16.
Alzheimer's disease (AD) research has entered a new era with the recent positive phase 3 clinical trials of the anti-Aβ antibodies lecanemab and donanemab. Why did it take 30 years to achieve these successes? Developing potent therapies for reducing fibrillar amyloid was key, as was selection of patients at relatively early stages of disease. Biomarkers of the target pathologies, including amyloid and tau PET, and insights from past trials were also critical to the recent successes. Moving forward, the challenge will be to develop more efficacious therapies with greater efficiency. Novel trial designs, including combination therapies and umbrella and basket protocols, will accelerate clinical development. Better diversity and inclusivity of trial participants are needed, and blood-based biomarkers may help to improve access for medically underserved groups. Incentivizing innovation in both academia and industry through public-private partnerships, collaborative mechanisms, and the creation of new career paths will be critical to build momentum in these exciting times.
阿尔茨海默病(AD)研究随着抗 Aβ 抗体 lecanemab 和 donanemab 的最近三期临床试验取得积极结果而进入了一个新时代。为什么要花 30 年才取得这些成功?开发出能够有效减少纤维状淀粉样蛋白的强力疗法是关键,选择疾病相对早期阶段的患者也是关键。目标病理学的生物标志物,包括淀粉样蛋白和 tau PET,以及过去试验的经验,对最近的成功也至关重要。展望未来,挑战将是开发更有效、更高效的疗法。新的试验设计,包括联合疗法、伞式和篮子式方案,将加速临床开发。需要更好地实现试验参与者的多样性和包容性,并且基于血液的生物标志物可能有助于改善医疗服务不足群体的可及性。通过公私合作伙伴关系、合作机制以及创建新的职业道路,激励学术界和工业界的创新,对于在这些令人兴奋的时代建立势头至关重要。