{"title":"Evaluación de la inmunoterapia con lecanemab para la enfermedad de Alzheimer: una revisión sistemática","authors":"Antía Villamediana-Pérez, Alejandro Ruiz-Riquelme","doi":"10.1016/j.sedene.2025.500190","DOIUrl":null,"url":null,"abstract":"<div><h3>Objective</h3><div>To critically examine the use of lecanemab as an immunotherapy for Alzheimer's disease, specifically to assess the benefits of such therapy, identify current dosing and administration recommendations, and assess potential side effects and exclusion criteria.</div></div><div><h3>Methods</h3><div>Systematic review of articles whose object of study are positive and/or negative results of lecanemab immunotherapy and include possible complications of the treatment. Articles presenting results of lecanemab immunotherapy in non-human models are excluded. The databases used for the search are Web of Science, Cochrane, Pubmed (Medline) and Dialnet.</div></div><div><h3>Results</h3><div>Eight articles (clinical studies, meta-analyses, simulations, case reports) are selected. The use of lecanemab in the early stages of Alzheimer's reduces cerebral Aβ and delays cognitive impairment. The dose established as effective is 10<!--> <!-->mg/kg biweekly, using an IV infusion for 1<!--> <!-->hour, followed by monitoring periods after each administration. Side effects may appear during the treatment like hemorrhages and cerebral edema (ARIA).</div></div><div><h3>Conclusions</h3><div>The effectiveness of lecanemab is associated with its use in the early stages of the development of the disease. The proper management of the dose and the side effects are fundamental, therefore providing clear protocols and training for the sanitary personnel are key for its implementation. The paucity of clinical studies on lecanemab treatment is a limitation to the results, making it necessary to periodically update reviews such as this one.</div></div>","PeriodicalId":38763,"journal":{"name":"Revista Cientifica de la Sociedad Espanola de Enfermeria Neurologica","volume":"64 ","pages":"Article 500190"},"PeriodicalIF":0.0000,"publicationDate":"2026-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Revista Cientifica de la Sociedad Espanola de Enfermeria Neurologica","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2013524625000170","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/4/28 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"Nursing","Score":null,"Total":0}
引用次数: 0
Abstract
Objective
To critically examine the use of lecanemab as an immunotherapy for Alzheimer's disease, specifically to assess the benefits of such therapy, identify current dosing and administration recommendations, and assess potential side effects and exclusion criteria.
Methods
Systematic review of articles whose object of study are positive and/or negative results of lecanemab immunotherapy and include possible complications of the treatment. Articles presenting results of lecanemab immunotherapy in non-human models are excluded. The databases used for the search are Web of Science, Cochrane, Pubmed (Medline) and Dialnet.
Results
Eight articles (clinical studies, meta-analyses, simulations, case reports) are selected. The use of lecanemab in the early stages of Alzheimer's reduces cerebral Aβ and delays cognitive impairment. The dose established as effective is 10 mg/kg biweekly, using an IV infusion for 1 hour, followed by monitoring periods after each administration. Side effects may appear during the treatment like hemorrhages and cerebral edema (ARIA).
Conclusions
The effectiveness of lecanemab is associated with its use in the early stages of the development of the disease. The proper management of the dose and the side effects are fundamental, therefore providing clear protocols and training for the sanitary personnel are key for its implementation. The paucity of clinical studies on lecanemab treatment is a limitation to the results, making it necessary to periodically update reviews such as this one.
目的:严格检查莱卡耐单抗作为阿尔茨海默病免疫疗法的使用,特别是评估这种疗法的益处,确定当前的剂量和给药建议,并评估潜在的副作用和排除标准。方法系统回顾研究对象为莱卡耐单抗免疫治疗阳性和/或阴性结果并包括治疗可能并发症的文章。在非人体模型中报道莱卡耐单抗免疫治疗结果的文章被排除在外。用于搜索的数据库是Web of Science、Cochrane、Pubmed (Medline)和Dialnet。结果8篇文章(临床研究、meta分析、模拟、病例报告)入选。在阿尔茨海默病的早期阶段使用莱卡耐单抗可以减少脑Aβ并延缓认知障碍。确定的有效剂量为每两周10 mg/kg,静脉输注1小时,每次给药后进行监测。在治疗过程中可能出现出血和脑水肿(ARIA)等副作用。结论lecanemab的有效性与其在疾病发展的早期阶段的使用有关。对剂量和副作用的适当管理是根本,因此为卫生人员提供明确的规程和培训是实施的关键。关于莱卡耐单抗治疗的临床研究的缺乏是对结果的限制,因此有必要定期更新综述,例如本综述。