Evidence map›Paper›PMID 41215623›Full record

ArticleBrain : a journal of neurology2026

Safety and short-term outcomes of lecanemab for Alzheimer's disease in China: a multicentre study.

Ling-Ling Li, Rong-Ze Wang, Zhen Wang, Hua Hu, Wei Xu, Lin Zhu, Yan Sun, Ke-Liang Chen, Shu-Fen Chen, Xiao-Yu He and 22 more

Abstract readMulticenter Study
In one paragraph

Article in Brain : a journal of neurology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Regulatory, clinical, and post-marketing challenges of lecanemab for Alzheimer's disease: insights from real-world data.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026
    Pooled it
  2. Lecanemab use in Chinese patients with Alzheimer's disease: a 12-month multicenter real-world study.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Observational
  3. Article
  4. Review
  5. Lecanemab treatment improves B cell subpopulation immune homeostasis in patients with Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Article
  6. White matterAlzheimer's research & therapy · 2026
    Article
  7. Observational
  8. Review
  9. Article
  10. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

32 authors.

Ling-Ling LiDepartment of Neurology and National Center for Neurological Disorders, Huashan Hospital, State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Shanghai Medical College, Fudan University, Shanghai 200040, China.
Rong-Ze WangDepartment of Neurology and National Center for Neurological Disorders, Huashan Hospital, State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Shanghai Medical College, Fudan University, Shanghai 200040, China.
Zhen WangDepartment of Geriatrics, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325000, China.ORCID 0000-0002-5671-3902
Hua HuDepartment of Neurology, The Second Affiliated Hospital of Soochow University, Soochow 215004, China.
Wei XuDepartment of Neurology, Qingdao Municipal Hospital Group, Qingdao 266000, China.
Lin ZhuDepartment of Neurology, Nanjing First Hospital, Nanjing Medical University, Nanjing 210006, China.
Yan SunDepartment of Neurology, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310031, China.
Ke-Liang ChenDepartment of Neurology and National Center for Neurological Disorders, Huashan Hospital, State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Shanghai Medical College, Fudan University, Shanghai 200040, China.
Shu-Fen ChenDepartment of Neurology and National Center for Neurological Disorders, Huashan Hospital, State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Shanghai Medical College, Fudan University, Shanghai 200040, China.
Xiao-Yu HeDepartment of Neurology and National Center for Neurological Disorders, Huashan Hospital, State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Shanghai Medical College, Fudan University, Shanghai 200040, China.
Ming-Yang YuanDepartment of Neurology and National Center for Neurological Disorders, Huashan Hospital, State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Shanghai Medical College, Fudan University, Shanghai 200040, China.
Yu-Yuan HuangDepartment of Neurology and National Center for Neurological Disorders, Huashan Hospital, State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Shanghai Medical College, Fudan University, Shanghai 200040, China.
Xiao-Yan LiuDepartment of Neurology, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310031, China.
Ping LiuDepartment of Neurology, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310031, China.
Qin-Yong YeDepartment of Neurology, Fujian Medical University Union Hospital, Fujian Key Laboratory of Molecular Neurology and Institute of Neuroscience, Fujian Medical University, Fuzhou 350402, China.
Jie WangDepartment of Neurology and National Center for Neurological Disorders, Huashan Hospital, State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Shanghai Medical College, Fudan University, Shanghai 200040, China.
Zi-Zhao JuDepartment of Nuclear Medicine & PET Center, Huashan Hospital, Fudan University, Shanghai 200040, China.
Wei ZhangInstitute of Science and Technology for Brain-Inspired Intelligence, Fudan University, Shanghai 200433, China.
Bin HuDepartment of Radiology, Huashan Hospital, Fudan University, Shanghai 200040, China.
Yu GuoDepartment of Neurology and National Center for Neurological Disorders, Huashan Hospital, State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Shanghai Medical College, Fudan University, Shanghai 200040, China.
Xiao-Yun CaoDepartment of Neurology, The Third Hospital of Hebei Medical University, Hebei 050051, China.
Yu-Xin LiDepartment of Radiology, Huashan Hospital, Fudan University, Shanghai 200040, China.
Chuan-Tao ZuoDepartment of Nuclear Medicine & PET Center, Huashan Hospital, Fudan University, Shanghai 200040, China.ORCID 0000-0002-8856-7217
Wei ChengInstitute of Science and Technology for Brain-Inspired Intelligence, Fudan University, Shanghai 200433, China.
Teng JiangDepartment of Neurology, Nanjing First Hospital, Nanjing Medical University, Nanjing 210006, China.
Lan TanDepartment of Neurology, Qingdao Municipal Hospital Group, Qingdao 266000, China.
Xiao-Chun ChenDepartment of Neurology, Fujian Medical University Union Hospital, Fujian Key Laboratory of Molecular Neurology and Institute of Neuroscience, Fujian Medical University, Fuzhou 350402, China.
Qian-Hua ZhaoDepartment of Neurology and National Center for Neurological Disorders, Huashan Hospital, State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Shanghai Medical College, Fudan University, Shanghai 200040, China.
Mei CuiDepartment of Neurology and National Center for Neurological Disorders, Huashan Hospital, State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Shanghai Medical College, Fudan University, Shanghai 200040, China.
Guo-Ping PengDepartment of Neurology, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310031, China.
Jia-Wei XinDepartment of Neurology, Fujian Medical University Union Hospital, Fujian Key Laboratory of Molecular Neurology and Institute of Neuroscience, Fujian Medical University, Fuzhou 350402, China.
Jin-Tai YuDepartment of Neurology and National Center for Neurological Disorders, Huashan Hospital, State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Shanghai Medical College, Fudan University, Shanghai 200040, China.ORCID 0000-0002-7686-0547

Funding

National Key Research and Development Program of China 2023YFC3605400
6 · The paper itself

Abstract

Lecanemab is a newly approved monoclonal antibody targeting amyloid plaques for the treatment of early Alzheimer's disease. This study aimed to evaluate the safety and short-term biomarkers and cognition changes of lecanemab in Chinese clinical practice. This multicentre real-world study involved patients receiving lecanemab treatment across seven hospitals in China. Patients underwent comprehensive assessments before treatment. Lecanemab was administered via intravenous infusion every 2 weeks. Treatment-related symptoms were monitored through self-report, and amyloid-related imaging abnormalities were assessed via magnetic resonance imaging. Amyloid and tau biomarker changes were measured using positron emission tomography imaging or plasma testing. Follow-up cognitive assessments were evaluated after 6 months of treatment. Short-term outcomes were analysed using linear mixed-effect models, without an untreated control group. A total of 407 patients who received at least one lecanemab infusion were involved in this study, with a mean follow-up time of 5.6 ± 3.39 months. The mean age was 68.08 years, with 67.57% of patients being female. Of the participants, 56.51% were apolipoprotein E (APOE) ε4 carriers, and 83.19% were at biological Stage C. During the study period, 22.22% of the patients experienced treatment-related symptoms, and 12.15% developed at least one amyloid-related imaging abnormality. Only four symptomatic and seven severe amyloid-related imaging abnormality cases were reported. APOE ε4 status was not related to adverse events in the Chinese population. Patients with a higher number of microhaemorrhages at baseline were more likely to develop adverse events. No significant differences in adverse events were observed between the moderate Alzheimer's disease dementia group and the mild cognitive impairment group. By the end of the research period, 9.38% of the patients withdrew from lecanemab. After 6 months of treatment, favourable short-term outcomes in biomarkers and stable cognitive function were observed. This study demonstrates that lecanemab treatment is feasible and well-tolerated among the Chinese population, with lower rates of adverse events and favourable short-term outcomes observed. Administration of lecanemab in the moderate Alzheimer's disease dementia population was relatively safe and further studies are warranted.

Indexed as

Alzheimer DiseaseAntibodies, MonoclonalAgedAged, 80 and overAmyloid beta-PeptidesBiomarkersChinaFemaleFollow-Up StudiesHumansMagnetic Resonance ImagingMaleMiddle AgedPositron-Emission Tomographytau ProteinsTreatment OutcomeAmyloid beta-PeptidesAntibodies, MonoclonalBiomarkerstau Proteinsdisease-modifying therapyinfusion-related reactionprophylactic treatment

Identifiers

PMID41215623
PMCPMC13232039

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