Villain Nicolas
AP-HP Sorbonne Université, Hôpital Pitié-Salpêtrière, Département de Neurologie, Institut de la Mémoire et de la Maladie d’Alzheimer, Paris, France
Institut du Cerveau – ICM, Sorbonne Université, INSERM U1127, CNRS 7225, Paris, France
Geriatr Psychol Neuropsychiatr Vieil. 2022 Jun 1;20(2):256-260. doi: 10.1684/pnv.2022.1042.
Research on disease-modifying treatments for Alzheimer’s disease has resulted in a series of failures over the past 20 years. However, in the last 4 years, five molecules have shown significant effects in phase II or III trials on clinical endpoints (i.e., slowing of cognitive decline). Among these five molecules, three are anti-amyloid immunotherapies: aducanumab, donanemab, and lecanemab responsible for a significant clearance of cerebral amyloid deposits. These results are still awaiting confirmation in order to put an end to the controversy surrounding the Food and Drug Administration’s decision to give conditional approval to aducanumab, which is considered premature by many specialists. Confirmation is also necessary to assess the benefit (magnitude of the slowing of decline) and risk (edema and cerebral hemorrhage induced by these treatments) balance of these molecules, which appears to be so far questionable after 18 months. Masitinib, a treatment whose probable mechanism of action is neuroinflammation, has also shown positive effects that need to be confirmed. Treatments targeting the tau protein are less advanced but weak signals are emerging from immunotherapies in the moderate stages of the disease (semorinemab). There is renewed hope for patients since it may not be unreasonable that these disease-modifying therapies will be part of the French therapeutic arsenal within the next five years.
在过去20年里,针对阿尔茨海默病的疾病修饰治疗研究遭遇了一系列失败。然而,在过去4年中,有5种分子在针对临床终点(即认知衰退减缓)的II期或III期试验中显示出显著效果。在这5种分子中,有3种是抗淀粉样蛋白免疫疗法:阿杜卡努单抗、多奈单抗和乐卡努单抗,它们能显著清除脑淀粉样蛋白沉积物。这些结果仍有待确认,以便结束围绕美国食品药品监督管理局有条件批准阿杜卡努单抗这一决定的争议,许多专家认为该批准为时过早。确认对于评估这些分子的益处(衰退减缓的程度)和风险(这些治疗引发的水肿和脑出血)平衡也很有必要,在18个月后,这种平衡目前看来仍存在疑问。马西替尼的可能作用机制是神经炎症,它也显示出了需要确认的积极效果。针对tau蛋白的治疗进展较慢,但在疾病中期的免疫疗法(司莫瑞单抗)中出现了微弱的积极信号。患者们有了新的希望,因为这些疾病修饰疗法在未来五年内成为法国治疗手段的一部分并非不合理。