Nelson J Craig, Rahman Zia, Laubmeier Kimberly K, Eudicone James M, McQuade Robert D, Berman Robert M, Marcus Ronald N, Baker Ross A, Sheehan John J
1Department of Psychiatry,University of California,San Francisco,California,USA.
2Medical Affairs Neuroscience Department,Bristol-Myers Squibb,Plainsboro,New Jersey,USA.
CNS Spectr. 2014 Dec;19(6):528-34. doi: 10.1017/S109285291300103X. Epub 2014 Mar 18.
Efficacy of depression treatments, including adjunctive antipsychotic treatment, has not been explored for patients with worsening symptoms after antidepressant therapy (ADT).
This post-hoc analysis utilized pooled data from 3 similarly designed, randomized, double-blind, placebo-controlled trials that assessed the efficacy, safety, and tolerability of adjunctive aripiprazole in patients with major depressive disorder with inadequate response to ADT. The studies had 2 phases: an 8-week prospective ADT phase and 6-week adjunctive (aripiprazole or placebo) treatment phase. This analysis focused on patients whose symptoms worsened during the prospective 8-week ADT phase (worsening defined as >0% increase in Montgomery-Åsberg Depressive Rating Scale [MADRS] Total score). During the 6-week, double-blind, adjunctive phase, response was defined as ≥50% reduction in MADRS Total score and remission as ≥50% reduction in MADRS Total score and MADRS score ≤10.
Of 1065 patients who failed to achieve a response during the prospective phase, 160 exhibited worsening of symptoms (ADT-Worseners), and 905 exhibited no change/reduction in MADRS scores (ADT-Non-worseners). Response rates for ADT-Worseners at endpoint were 36.6% (adjunctive aripiprazole) and 22.5% (placebo). Similarly, response rates at endpoint for ADT-Non-worseners were 37.5% (adjunctive aripiprazole) and 22.5% (placebo). Remission rates at endpoint for ADT-Worseners were 25.4% (adjunctive aripiprazole) and 12.4% (placebo). For ADT-Non-worseners, remission rates were 29.9% (adjunctive aripiprazole) and 17.4% (placebo).
These results suggest that adjunctive aripiprazole is an effective intervention for patients whose symptoms worsen during antidepressant monotherapy. The results challenge the view that benefits of adjunctive therapy with aripiprazole are limited to partial responders to ADT.
对于抗抑郁治疗(ADT)后症状恶化的患者,包括辅助使用抗精神病药物治疗在内的抑郁症治疗效果尚未得到研究。
这项事后分析利用了来自3项设计相似、随机、双盲、安慰剂对照试验的汇总数据,这些试验评估了辅助使用阿立哌唑对重度抑郁症且对ADT反应不足患者的疗效、安全性和耐受性。研究分为两个阶段:一个为期8周的前瞻性ADT阶段和一个为期6周的辅助(阿立哌唑或安慰剂)治疗阶段。该分析聚焦于在前瞻性8周ADT阶段症状恶化的患者(恶化定义为蒙哥马利-阿斯伯格抑郁评定量表[MADRS]总分增加>0%)。在为期6周的双盲辅助阶段,反应定义为MADRS总分降低≥50%,缓解定义为MADRS总分降低≥50%且MADRS评分≤10。
在前瞻性阶段未达到反应的1065例患者中,160例出现症状恶化(ADT恶化者),905例MADRS评分无变化/降低(ADT未恶化者)。ADT恶化者在终点时的反应率分别为36.6%(辅助使用阿立哌唑)和22.5%(安慰剂)。同样,ADT未恶化者在终点时的反应率分别为37.5%(辅助使用阿立哌唑)和22.5%(安慰剂)。ADT恶化者在终点时的缓解率分别为25.4%(辅助使用阿立哌唑)和12.4%(安慰剂)。对于ADT未恶化者,缓解率分别为29.9%(辅助使用阿立哌唑)和17.4%(安慰剂)。
这些结果表明,辅助使用阿立哌唑对在抗抑郁单药治疗期间症状恶化的患者是一种有效的干预措施。这些结果挑战了阿立哌唑辅助治疗的益处仅限于对ADT部分反应者的观点。