靶向淀粉样蛋白病理在早期阿尔茨海默病:Donanemab-Azbt的前景。

IF 2.2 Q3 PHARMACOLOGY & PHARMACY Pharmacy Pub Date : 2025-02-08 DOI:10.3390/pharmacy13010023
Nadia Khartabil, Ayda Awaness
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引用次数: 0

摘要

目的:本综述的目的是研究donanemab-azbt在早期阿尔茨海默病(AD)治疗和管理中的潜在作用,重点关注其疗效、安全性和基于关键临床试验数据的临床相关性。资料来源:使用“donanemab”、“Alzheimer’s disease”、“Kisunla”、“TRAILBLAZER临床试验”、“淀粉样蛋白相关成像异常(ARIA)”等相关关键词,综合检索PubMed文献。其他数据从临床试验记录(clinicaltrials.gov)、会议摘要和产品专著中提取。研究选择和数据提取:仅包括在人群中进行的英语研究。临床试验和同行评审的研究详细说明了donanemab-azbt的疗效、安全性和机制的见解是优先考虑的。数据综合:TRAILBLAZER系列临床试验的主要发现强调了donanemab-azbt在减缓早期AD认知和功能下降方面的潜力:(1)TRAILBLAZER- alz(2期):该试验侧重于tau蛋白水平中等的参与者。结果显示,统计上显著减缓了认知和功能衰退。(2) TRAILBLAZER-ALZ 2(3期):一项大规模、随机、双盲、安慰剂对照研究证实了donanemab-azbt在减少淀粉样斑块积累和认知能力下降方面的疗效。主要结果包括阿尔茨海默病综合评分量表(iADRS)下降速度减缓35%,临床痴呆评分-盒子总数(CDR-SB)下降速度减缓36%。其他次要结果显示日常生活活动的改善和疾病进展风险的降低。(3) TRAILBLAZER-ALZ 3:这项正在进行的试验正在评估donanemab在患有淀粉样斑块的认知正常个体中延缓或预防阿尔茨海默氏症的潜力,扩大早期干预策略的范围。(4) TRAILBLAZER-ALZ 4:与aducanumab的头对头比较显示donanemab具有更好的淀粉样斑块清除能力。(5) TRAILBLAZER-ALZ 5:目前正在招募,该试验旨在评估具有不同tau水平和合并症的不同人群的安全性和有效性。(6) TRAILBLAZER-ALZ 6 (3b期):该试验研究了改进的给药方案,以减少ARIA,同时保持疗效,特别是在具有遗传风险因素(如ApoE ε4纯合子)的人群中。与患者护理和临床实践的相关性:Donanemab-azbt代表了早期AD患者的一种有希望的治疗选择。它专门针对并减少淀粉样蛋白斑块,这是该疾病的一个标志,有可能减缓进展并保持认知功能。然而,它的使用需要谨慎的患者选择,包括ApoE ε4状态的基因检测,以降低ARIA的风险。此外,研究结果强调了在治疗期间密切监测的重要性。结论:Donanemab-azbt为治疗早期AD提供了新的途径,有望减少淀粉样蛋白负担和减缓认知能力下降。虽然其有效性和安全性已在临床试验中得到证实,但必须进一步研究以验证长期结果,评估不同人群的有效性,并改进给药策略以尽量减少副作用。随着研究的继续,donanemab-azbt可能会显著影响阿尔茨海默病治疗的临床前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Targeting Amyloid Pathology in Early Alzheimer's: The Promise of Donanemab-Azbt.

Objective: The purpose of this review is to examine the potential role of donanemab-azbt in the treatment and management of early-stage Alzheimer's disease (AD), with a focus on its efficacy, safety, and clinical relevance based on data from key clinical trials.

Data sources: A comprehensive literature search of PubMed was conducted using relevant keywords such as "donanemab", "Alzheimer's disease", "Kisunla", "TRAILBLAZER clinical trials", and "amyloid-related imaging abnormalities (ARIA)". Additional data were extracted from clinical trial records (clinicaltrials.gov), conference abstracts, and product monographs.

Study selection and data extraction: Only English-language studies conducted in human populations were included. Clinical trials and peer-reviewed studies detailing the efficacy, safety, and mechanistic insights of donanemab-azbt were prioritized.

Data synthesis: Key findings from the TRAILBLAZER series of clinical trials highlighted the potential of donanemab-azbt in slowing cognitive and functional decline in early-stage AD: (1) TRAILBLAZER-ALZ (Phase 2): This trial focused on participants with intermediate levels of tau protein. Results demonstrated a statistically significant slowing of cognitive and functional decline. (2) TRAILBLAZER-ALZ 2 (Phase 3): A large-scale, randomized, double-blind, placebo-controlled study confirmed the efficacy of donanemab-azbt in reducing amyloid plaque accumulation and cognitive decline. Key results included a 35% slowing of decline on the Integrated Alzheimer's Disease Rating Scale (iADRS) and a 36% slowing on the Clinical Dementia Rating-Sum of Boxes (CDR-SB). Additional secondary outcomes showed improvements in activities of daily living and reduced risk of disease progression. (3) TRAILBLAZER-ALZ 3: This ongoing trial is evaluating donanemab's potential in delaying or preventing Alois Alzheimer in cognitively normal individuals with amyloid plaques, broadening the scope of early intervention strategies. (4) TRAILBLAZER-ALZ 4: A head-to-head comparison with aducanumab revealed superior amyloid plaque clearance with donanemab. (5) TRAILBLAZER-ALZ 5: Currently recruiting, this trial aims to evaluate safety and efficacy across diverse populations with varying tau levels and comorbidities. (6) TRAILBLAZER-ALZ 6 (Phase 3b): This trial investigates modified dosing regimens to reduce ARIA while maintaining efficacy, particularly in populations with genetic risk factors like ApoE ε4 homozygotes.

Relevance to patient care and clinical practice: Donanemab-azbt represents a promising treatment option for patients with early-stage AD. It specifically targets and reduces amyloid beta plaques, a hallmark of the disease, potentially slowing progression and preserving cognitive function. However, its administration requires careful patient selection, including genetic testing for ApoE ε4 status, to mitigate risks of ARIA. Furthermore, the findings emphasize the importance of close monitoring during treatment.

Conclusions: Donanemab-azbt offers a new avenue for managing early-stage AD, showing promise in reducing amyloid burden and slowing cognitive decline. While its efficacy and safety have been demonstrated in clinical trials, further research is essential to validate long-term outcomes, assess effectiveness across diverse populations, and refine dosing strategies to minimize side effects. With continued investigation, donanemab-azbt could significantly impact the clinical landscape of AD treatment.

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Pharmacy
Pharmacy PHARMACOLOGY & PHARMACY-
自引率
9.10%
发文量
141
审稿时长
11 weeks
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