An Observational Study on Lecanemab Treatment for Early Alzheimer's Disease

Zhejiang University

Status: Enrolling

Conditions: Alzheimer Disease

Study type: Observational

Funder types: Other

Identifiers

NCT07153848

lecanamab and biomarkers

Details and patient eligibility

About

The goal of this observational study is to valuate the sensitivity and specificity of different blood biomarkers for monitoring and assessing Aβ-PET-confirmed mitigation of amyloid pathology by lencanumab treatment in subjects treated with lencanumab.

Full description

This study was a prospective observational study of a patient population treated or planning to be treated with lencanemab from a multicenter cohort of patients with early-stage AD in Zhejiang Province. It was a real-world study based on the treatment of lencanemab. The primary enrollment population was patients with mild AD or mild AD-origin cognitive disorders who had completed positive Aβ-PET scans that met the PET quality-control criteria and who were receiving treatment with lencanemab. Patients with cognitive impairment were divided into two subgroups: those receiving donepezil treatment alone and those receiving lencanemab combined with standard treatment with donepezil. Fresh plasma was collected at baseline, 3 months of follow-up, 6 months of follow-up, 12 months of follow-up, and 18 months of follow-up, respectively. Amyloid PET scanning was performed at 12 months of follow-up and 18 months of follow-up. In order to evaluate the sensitivity and specificity of different blood biomarkers for monitoring and assessing the alleviation of amyloid pathology progression by Aβ-PET-confirmed lencanumab treatment, blinded peripheral blood AD core marker assays were performed in the main central laboratory. Furthermore, the aim was to provide a follow-up tool suitable for clinical blood marker-based monitoring of lencanumab treatment.

Enrollment: 400 estimated patients

Sex: All

Ages: 45 to 85 years old

Volunteers: Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion criteria (all of the following must be met simultaneously):

Mild Alzheimer's Disease (AD):

1. Age ≥ 45 years but ≤ 85 years;
2. Literacy level of elementary school and above (i.e., ≥3 years of education);
3. Fulfillment of the diagnostic criteria for probable AD in the NINCDS-ADRDA 2007 revision (or the diagnostic criteria for clinically probable AD in the National Institute on Aging and Alzheimer's Disease Association NIA-AA 2011 edition);
4. Clinical Dementia Rating Scale CDR-global = 1 point;
5. Aβ-PET scan suggesting extensive deposition of Aβ plaques in the brain.

AD-derived mild cognitive impairment (aMCI) inclusion criteria (must meet all of the following conditions at the same time):

1. Age: 45 years or older but ≤85 years;

2. Literacy level elementary school and above (i.e., ≥3 years of education);

3. Meeting Peterson's 2004 diagnostic criteria for MCI:

   (i) Complaint of memory impairment that can be confirmed by an informed person; (ii) objective evidence of memory impairment (memory test scores 1-1.5 standard deviations below normal controls matched for age and literacy; e.g., Huashan Hospital's recommended cut-off values for those with elementary school literacy or above are as follows: long-delayed recall 50-59 years old ≤ 5, 60-69 years old ≤ 4, 70-79 years old ≤ 3, 80-89 years old ≤ 2, or re-recognition scores of 50-59 years old ≤ 20, 60-69 age ≤19 points, 70-79 years ≤18 points, 80-89 years ≤16 points); (iii) Overall cognitive functioning was largely preserved, with CDR-global = 0.5 points and MMSE: ≥24 points for those with junior high school or higher education used in this study;

   ④ Daily life ability remains normal (basically able to complete going out by transportation and shopping and counting, etc.);

   ⑤ Does not meet the International Classification of Diseases Diagnostic Manual, 10th edition dementia criteria (for research purposes) and the National Institute of Neurological and Speech-Language Disorders and Stroke, Alzheimer's Disease and Related Disorders Association (NINCDS-ADRDA) likely diagnostic criteria for AD dementia; (vi) Aβ-PET scan suggested extensive deposition of Aβ plaques in the brain.

Normal control Inclusion criteria (all of the following must be met simultaneously).

1. Age ≥55 years but ≤85 years;
2. Elementary school 3 years of education and above;
3. MMSE: ≥26 points for those with junior high school or higher education;
4. CDR=0;
5. Activity of Daily Living Scale (ADL) score ≤ 20;
6. No significant deposition of Abeta in the brain as indicated by Aβ-PET scan.

Exclusion Criteria (excluded if any of the following conditions were met):

1. Those with a history of stroke and neurologic focal signs, head MRI scans excluding external infarct foci, brain softening foci and other occupying lesions, etc., as well as SWI sequences showing 5 or more microhemorrhagic foci, vascular malformations, etc;
2. Presence of other neurological disorders that may cause brain dysfunction (e.g., schizophrenia, severe anxiety and depression, frontotemporal lobe dementia, Huntington's disease, brain tumors, Parkinson's disease, metabolic encephalopathy, encephalitis, multiple sclerosis, epilepsy, traumatic brain injury, and normal cranial pressure hydrocephalus, etc.);
3. Presence of other systemic diseases that can cause cognitive impairment, such as hypothyroidism, folic acid and vitamin B12 deficiency, specific infections (e.g., syphilis, HIV), alcohol and drug abuse;
4. Presence of a history of severe hepatic or renal insufficiency, severe pulmonary insufficiency, severe anemia, severe gastrointestinal disorders, severe cardiac arrhythmias, cardiac infarction within 6 months, and malignant tumors;
5. Oral anticoagulants (including warfarin and new oral anticoagulants, etc.);
6. Presence of contraindications to NMR such as metal implantation in the body;
7. Diseases such as aphasia, impaired consciousness, etc. that prevent cooperation in completing the cognitive examination;
8. Refusal to sign the informed consent.

Trial design

400 participants in 2 patient groups

donepezil treatment

Description:

In this cohort, a standardized treatment regimen of donepezil at a dose of 10 mg was employed.

donepezil and lencanemab treatment

Description:

The group was treated with a combination regimen of lencanumab and donepezil. Lencanumab was administered at a dose of 10 mg/kg every two weeks, while donepezil was used at a dose of 10 mg per day.