Rockwood K, Mintzer J, Truyen L, Wessel T, Wilkinson D
Centre for Health Care of the Elderly, QEII Health Sciences Centre, 1421-5955 Veterans' Memorial Lane, Halifax, Canada B3H 2E1.
J Neurol Neurosurg Psychiatry. 2001 Nov;71(5):589-95. doi: 10.1136/jnnp.71.5.589.
To assess the efficacy and safety of galantamine in Alzheimer's disease at 3 months using flexible dose escalation.
A randomised, double blind, placebo controlled trial in 43 centres in the United States, Canada, Great Britain, South Africa, Australia, and New Zealand. Patients with probable Alzheimer's disease (n=386; 171 women) with a score of 11-24 on the mini mental state examination, and a score> or =12 on the cognitive subscale of the Alzheimer's disease assessment scale (ADAS-cog) were randomised to placebo, or galantamine escalated over 4 weeks to a maintenance dose of 24 or 32 mg/day. The primary outcome measures were the change in ADAS-cog score and the clinician's interview based impression of change plus caregiver input (CIBIC-plus) score. Activities of daily living (ADL) and behavioural symptoms were secondary outcomes. To compare the effects of highest levels of dosing, an observed cases (OC) analysis was undertaken, with classic intention to treat (ITT) and ITT with last observation carried forward (LOCF) as confirmatory analyses.
At 3 months, galantamine (24-32 mg/day) produced a significantly better outcome on cognitive function than placebo (treatment difference=1.9 points on ADAS-cog, p=0.002) and a significantly better global response than placebo, as measured by CIBIC-plus (deterioration in 21% of patients on galantamine v 37% on placebo; p<0.001). Galantamine produced significant benefits on basic and instrumental ADL. Behavioural symptoms did not change significantly from baseline levels in either group. Adverse events (primarily gastrointestinal) were of mild to moderate intensity. There were no important differences between the OC, ITT, and ITT/LOCF analyses. Most patients (82%) who were maintained on the higher dose of galantamine completed the study.
Patients on galantamine, compared with those on placebo, experienced benefits in cognitive function and instrumental and basic activities of daily living. Flexible dose escalation of galantamine was well tolerated.
采用灵活剂量递增法评估加兰他敏治疗阿尔茨海默病3个月时的疗效和安全性。
在美国、加拿大、英国、南非、澳大利亚和新西兰的43个中心进行的一项随机、双盲、安慰剂对照试验。简易精神状态检查得分11 - 24分,阿尔茨海默病评估量表认知分量表(ADAS - cog)得分≥12分的可能患有阿尔茨海默病的患者(n = 386;171名女性)被随机分配至安慰剂组,或加兰他敏组,加兰他敏在4周内递增至维持剂量24或32毫克/天。主要结局指标为ADAS - cog得分的变化以及基于临床医生访谈的变化印象加照料者意见(CIBIC-plus)得分。日常生活活动(ADL)和行为症状为次要结局指标。为比较最高剂量水平的效果,进行了观察病例(OC)分析,并采用经典意向性分析(ITT)和末次观察结转(LOCF)的ITT分析作为确证性分析。
3个月时,加兰他敏(24 - 32毫克/天)在认知功能方面的结局显著优于安慰剂(ADAS - cog治疗差异为1.9分,p = 0.002),且根据CIBIC-plus评估,整体反应显著优于安慰剂(加兰他敏组21%的患者病情恶化,安慰剂组为37%;p < 0.001)。加兰他敏对基本和工具性ADL有显著益处。两组的行为症状与基线水平相比均无显著变化。不良事件(主要为胃肠道事件)为轻度至中度。OC、ITT和ITT/LOCF分析之间无重要差异。大多数维持较高剂量加兰他敏治疗的患者(82%)完成了研究。
与服用安慰剂的患者相比,服用加兰他敏的患者在认知功能以及工具性和基本日常生活活动方面有所获益。加兰他敏灵活剂量递增耐受性良好。