From the Department of Neurology (V.K.R., L.K.J.), Mayo Clinic, Rochester, MN; Department of Neurology (M.J.A.), University of Florida College of Medicine; Norman Fixel Institute for Neurologic Diseases (M.J.A.), University of Florida, Gainesville; Cleo Roberts Center (P.C.), Banner Sun Health Research Institute, Sun City, AZ; Rocky Mountain Neurology (K.C.), Lone Tree, CO; Department of Neurology (R.H.H., D.A.W.), Department of Physical Medicine and Rehabilitation (R.H.H.), and Department of Psychiatry (R.H.H.), University of Pennsylvania Perelman School of Medicine, Philadelphia; Abington Neurological Associates (B.C.K.), Ltd., Abington, PA; and American Academy of Neurology (S.R.W.), Minneapolis, MN.
Neurology. 2023 Nov 7;101(19):842-852. doi: 10.1212/WNL.0000000000207757. Epub 2023 Jul 26.
With recent data demonstrating that lecanemab treatment can slow cognitive and functional decline in early symptomatic Alzheimer disease (AD), it is widely anticipated that this drug and potentially other monoclonal antibody infusions targeting β-amyloid protein will imminently be realistic options for some patients with AD. Given that these new antiamyloid monoclonal antibodies (mAbs) are associated with nontrivial risks and burdens of treatment that are radically different from current mainstays of AD management, effectively and equitably translating their use to real-world clinical care will require systematic and practice-specific modifications to existing workflows and infrastructure. In this Emerging Issues in Neurology article, we provide practical guidance for a wide audience of neurology clinicians on logistic adaptations and decision making around emerging antiamyloid mAbs. Specifically, we briefly summarize the rationale and available evidence supporting antiamyloid mAb use in AD to facilitate appropriate communication with patients and care partners on potential benefits. We also discuss pragmatic approaches to optimizing patient selection and treatment monitoring, with a particular focus on the value of incorporating shared decision making and multidisciplinary collaboration. In addition, we review some of the recognized limitations of current knowledge and highlight areas of future evolution to guide the development of sustainable and flexible models for treatment and follow-up. As the field enters a new era with disease-modifying treatment options for AD, it will be critical for neurology practices to prepare and continually innovate to ensure optimal outcomes for patients.
鉴于最近的数据表明仑卡奈单抗治疗可以减缓早期有症状阿尔茨海默病(AD)的认知和功能下降,预计这种药物以及可能针对β-淀粉样蛋白的其他单克隆抗体输注将很快成为一些 AD 患者的现实选择。鉴于这些新的抗淀粉样蛋白单克隆抗体(mAbs)与治疗的重大风险和负担有关,这些风险和负担与 AD 管理的当前主要治疗方法截然不同,因此要将其有效且公平地应用于现实临床护理,需要对现有工作流程和基础设施进行系统和特定于实践的修改。在这篇新兴神经学问题文章中,我们为广大神经科临床医生提供了关于新兴抗淀粉样蛋白 mAbs 的后勤适应和决策的实用指导。具体来说,我们简要总结了支持 AD 中使用抗淀粉样蛋白 mAbs 的基本原理和现有证据,以促进与患者和护理伙伴就潜在益处进行适当沟通。我们还讨论了优化患者选择和治疗监测的实用方法,特别强调了采用共同决策和多学科合作的价值。此外,我们回顾了当前知识的一些公认局限性,并强调了未来发展的领域,以指导治疗和随访的可持续和灵活模式的发展。随着 AD 疾病修饰治疗选择进入新时代,神经科实践必须做好准备并不断创新,以确保为患者提供最佳结果。