Park Kee Hyung, Kim Geon Ha, Kim Chi-Hun, Koh Seong-Ho, Moon So Young, Park Young Ho, Seo Sang Won, Yoon Bora, Lim Jae-Sung, Kim Byeong C, Kim Hee-Jin, Na Hae Ri, Shim YongSoo, Yang YoungSoon, Lee Chan-Nyoung, Rhee Hak Young, Jung San, Jeong Jee Hyang, Choi Hojin, Yang Dong Won, Choi Seong Hye
Department of Neurology, Gachon University Gil Medical Center, Gachon University College of Medicine, Incheon, Korea.
Department of Neurology, Ewha Womans University Mokdong Hospital, Ewha Womans University College of Medicine, Seoul, Korea.
Dement Neurocogn Disord. 2024 Oct;23(4):165-187. doi: 10.12779/dnd.2024.23.4.165. Epub 2024 Oct 29.
Lecanemab (product name Leqembi®) is an anti-amyloid monoclonal antibody treatment approved for use in Korea for patients with mild cognitive impairment (MCI) or mild dementia due to Alzheimer's disease. The Korean Dementia Association has created recommendations for the appropriate use of lecanemab to assist clinicians. These recommendations include selecting patients for administration, necessary pre-administration tests and preparations, administration methods, monitoring for amyloid related imaging abnormalities (ARIA), and communication with patients and caregivers. Lecanemab is recommended for patients with MCI or mild dementia who confirmed positive amyloid biomarkers, and should not be administered to patients with severe hypersensitivity to lecanemab or those unable to undergo magnetic resonance imaging (MRI) evaluation. To predict the risk of ARIA before administration, apolipoprotein E genotyping is conducted, and regular brain MRI evaluations are recommended to monitor for ARIA during treatment. The most common adverse reactions are infusion-related reactions, which require appropriate management upon occurrence. Additional caution is needed when co-administering with anticoagulants or tissue plasminogen activator due to the risk of macrohemorrhage. Clinicians should consider the efficacy and necessary conditions for administration, as well as the safety of lecanemab, to make a comprehensive decision regarding its use.
仑卡奈单抗(商品名:Leqembi®)是一种抗淀粉样蛋白单克隆抗体治疗药物,在韩国被批准用于治疗因阿尔茨海默病导致的轻度认知障碍(MCI)或轻度痴呆患者。韩国痴呆症协会制定了仑卡奈单抗的合理使用建议,以协助临床医生。这些建议包括选择给药患者、给药前必要的检查和准备、给药方法、监测淀粉样蛋白相关成像异常(ARIA)以及与患者和护理人员沟通。仑卡奈单抗推荐用于淀粉样蛋白生物标志物检测呈阳性的MCI或轻度痴呆患者,对仑卡奈单抗严重过敏或无法进行磁共振成像(MRI)评估的患者不应使用。给药前进行载脂蛋白E基因分型以预测ARIA风险,治疗期间建议定期进行脑部MRI评估以监测ARIA。最常见的不良反应是输液相关反应,发生时需要进行适当处理。由于存在大出血风险,与抗凝剂或组织纤溶酶原激活剂合用时需要格外谨慎。临床医生应考虑给药的疗效和必要条件以及仑卡奈单抗的安全性,以就其使用做出全面决策。