对抗抑郁药物治疗反应最小或部分的重性抑郁症患者的辅助布雷哌唑:随机对照试验的事后分析

IF 3.7 2区 医学 Q1 CLINICAL NEUROLOGY
Shivani Kapadia, Zhen Zhang, Ferhat Ardic, Mehul Patel, Michael E Thase, George I Papakostas
{"title":"对抗抑郁药物治疗反应最小或部分的重性抑郁症患者的辅助布雷哌唑:随机对照试验的事后分析","authors":"Shivani Kapadia, Zhen Zhang, Ferhat Ardic, Mehul Patel, Michael E Thase, George I Papakostas","doi":"10.1093/ijnp/pyaf074","DOIUrl":null,"url":null,"abstract":"<p><strong>Importance: </strong>Many patients with major depressive disorder (MDD) have <50% symptom reduction on antidepressant treatment, and may benefit from an adjunctive atypical antipsychotic.</p><p><strong>Objective: </strong>To investigate the efficacy and safety of adjunctive brexpiprazole in patients with minimal (>0% to <25%) and partial (≥25 to <50%) response to antidepressant treatment.</p><p><strong>Design: </strong>Data were pooled from three international, 6-week, randomized, double-blind, placebo-controlled, Phase 3 trials.</p><p><strong>Setting: </strong>Outpatient.</p><p><strong>Participants: </strong>Adults with MDD and inadequate response to antidepressant treatments. Patients were stratified into minimal and partial response subgroups based on their response over an 8-week prospective antidepressant treatment period.</p><p><strong>Interventions: </strong>Adjunctive brexpiprazole 2-3 mg/day or adjunctive placebo.</p><p><strong>Main outcomes and measures: </strong>Efficacy was assessed using the Montgomery-Åsberg Depression Rating Scale (MADRS) and the Clinical Global Impressions - Severity of illness (CGI-S) in the 6-week randomized adjunctive treatment period. Safety was assessed by treatment-emergent adverse events (TEAEs).</p><p><strong>Results: </strong>In patients with minimal response to antidepressant treatment (n = 663), least squares (LS) mean (SE) MADRS total score change over the randomized treatment period was -8.8 (0.3) points for antidepressant + brexpiprazole and -6.3 (0.3) points for antidepressant + placebo; the LS mean difference at Week 6 was -2.47 (95% CI, -3.38 to -1.55); p<.001; Cohen's d, 0.41. In patients with partial response to antidepressant treatment (n = 235), corresponding changes were -6.4 (0.5) and -4.9 (0.5) points; LS mean difference, -1.53 (-2.94 to -0.11); p=.035; Cohen's d, 0.28. CGI-S results aligned with MADRS results. In patients with minimal response to antidepressant treatment, the incidence of TEAEs was 196/328 (59.8%) for antidepressant + brexpiprazole and 160/335 (47.8%) for antidepressant + placebo. In patients with partial response to antidepressant treatment, corresponding values were 63/115 (54.8%) and 49/120 (40.8%).</p><p><strong>Conclusions and relevance: </strong>Adjunctive brexpiprazole may be efficacious in MDD regardless of whether patients show minimal or partial response to antidepressant treatment.</p><p><strong>Trial registration: </strong>Post hoc analysis of NCT01360645, NCT01360632, NCT02196506 (ClinicalTrials.gov).</p>","PeriodicalId":14134,"journal":{"name":"International Journal of Neuropsychopharmacology","volume":" ","pages":""},"PeriodicalIF":3.7000,"publicationDate":"2025-10-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Adjunctive brexpiprazole in patients with major depressive disorder who show minimal or partial response to antidepressant treatment: post hoc analysis of randomized controlled trials.\",\"authors\":\"Shivani Kapadia, Zhen Zhang, Ferhat Ardic, Mehul Patel, Michael E Thase, George I Papakostas\",\"doi\":\"10.1093/ijnp/pyaf074\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Importance: </strong>Many patients with major depressive disorder (MDD) have <50% symptom reduction on antidepressant treatment, and may benefit from an adjunctive atypical antipsychotic.</p><p><strong>Objective: </strong>To investigate the efficacy and safety of adjunctive brexpiprazole in patients with minimal (>0% to <25%) and partial (≥25 to <50%) response to antidepressant treatment.</p><p><strong>Design: </strong>Data were pooled from three international, 6-week, randomized, double-blind, placebo-controlled, Phase 3 trials.</p><p><strong>Setting: </strong>Outpatient.</p><p><strong>Participants: </strong>Adults with MDD and inadequate response to antidepressant treatments. Patients were stratified into minimal and partial response subgroups based on their response over an 8-week prospective antidepressant treatment period.</p><p><strong>Interventions: </strong>Adjunctive brexpiprazole 2-3 mg/day or adjunctive placebo.</p><p><strong>Main outcomes and measures: </strong>Efficacy was assessed using the Montgomery-Åsberg Depression Rating Scale (MADRS) and the Clinical Global Impressions - Severity of illness (CGI-S) in the 6-week randomized adjunctive treatment period. Safety was assessed by treatment-emergent adverse events (TEAEs).</p><p><strong>Results: </strong>In patients with minimal response to antidepressant treatment (n = 663), least squares (LS) mean (SE) MADRS total score change over the randomized treatment period was -8.8 (0.3) points for antidepressant + brexpiprazole and -6.3 (0.3) points for antidepressant + placebo; the LS mean difference at Week 6 was -2.47 (95% CI, -3.38 to -1.55); p<.001; Cohen's d, 0.41. In patients with partial response to antidepressant treatment (n = 235), corresponding changes were -6.4 (0.5) and -4.9 (0.5) points; LS mean difference, -1.53 (-2.94 to -0.11); p=.035; Cohen's d, 0.28. CGI-S results aligned with MADRS results. In patients with minimal response to antidepressant treatment, the incidence of TEAEs was 196/328 (59.8%) for antidepressant + brexpiprazole and 160/335 (47.8%) for antidepressant + placebo. In patients with partial response to antidepressant treatment, corresponding values were 63/115 (54.8%) and 49/120 (40.8%).</p><p><strong>Conclusions and relevance: </strong>Adjunctive brexpiprazole may be efficacious in MDD regardless of whether patients show minimal or partial response to antidepressant treatment.</p><p><strong>Trial registration: </strong>Post hoc analysis of NCT01360645, NCT01360632, NCT02196506 (ClinicalTrials.gov).</p>\",\"PeriodicalId\":14134,\"journal\":{\"name\":\"International Journal of Neuropsychopharmacology\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":3.7000,\"publicationDate\":\"2025-10-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Neuropsychopharmacology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1093/ijnp/pyaf074\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CLINICAL NEUROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Neuropsychopharmacology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1093/ijnp/pyaf074","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

摘要

重要性:许多重度抑郁症(MDD)患者有以下症状:目的:探讨辅助布雷吡拉唑治疗的有效性和安全性:数据来自3个国际、6周、随机、双盲、安慰剂对照的3期试验。设置:门诊。参与者:患有重度抑郁症且对抗抑郁药物治疗反应不足的成年人。根据患者在8周的预期抗抑郁治疗期间的反应,将患者分为最小反应和部分反应亚组。干预措施:辅助布雷哌唑2-3毫克/天或辅助安慰剂。主要结局和措施:在6周随机辅助治疗期间,使用Montgomery-Åsberg抑郁评定量表(MADRS)和临床总体印象-疾病严重程度(CGI-S)评估疗效。安全性通过治疗中出现的不良事件(teae)进行评估。结果:在对抗抑郁药物治疗反应最小的患者(n = 663)中,抗抑郁药物+ brexpiprazole的最小二乘(LS) mean (SE) MADRS总分在随机治疗期间的变化为-8.8(0.3)分,抗抑郁药物+安慰剂的最小二乘(SE)总分变化为-6.3(0.3)分;第6周的LS平均差异为-2.47 (95% CI, -3.38至-1.55);结论及相关性:无论患者对抗抑郁药物治疗是否表现出最小或部分反应,辅助布雷吡拉唑可能对重度抑郁症有效。试验注册:NCT01360645、NCT01360632、NCT02196506的事后分析(ClinicalTrials.gov)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Adjunctive brexpiprazole in patients with major depressive disorder who show minimal or partial response to antidepressant treatment: post hoc analysis of randomized controlled trials.

Importance: Many patients with major depressive disorder (MDD) have <50% symptom reduction on antidepressant treatment, and may benefit from an adjunctive atypical antipsychotic.

Objective: To investigate the efficacy and safety of adjunctive brexpiprazole in patients with minimal (>0% to <25%) and partial (≥25 to <50%) response to antidepressant treatment.

Design: Data were pooled from three international, 6-week, randomized, double-blind, placebo-controlled, Phase 3 trials.

Setting: Outpatient.

Participants: Adults with MDD and inadequate response to antidepressant treatments. Patients were stratified into minimal and partial response subgroups based on their response over an 8-week prospective antidepressant treatment period.

Interventions: Adjunctive brexpiprazole 2-3 mg/day or adjunctive placebo.

Main outcomes and measures: Efficacy was assessed using the Montgomery-Åsberg Depression Rating Scale (MADRS) and the Clinical Global Impressions - Severity of illness (CGI-S) in the 6-week randomized adjunctive treatment period. Safety was assessed by treatment-emergent adverse events (TEAEs).

Results: In patients with minimal response to antidepressant treatment (n = 663), least squares (LS) mean (SE) MADRS total score change over the randomized treatment period was -8.8 (0.3) points for antidepressant + brexpiprazole and -6.3 (0.3) points for antidepressant + placebo; the LS mean difference at Week 6 was -2.47 (95% CI, -3.38 to -1.55); p<.001; Cohen's d, 0.41. In patients with partial response to antidepressant treatment (n = 235), corresponding changes were -6.4 (0.5) and -4.9 (0.5) points; LS mean difference, -1.53 (-2.94 to -0.11); p=.035; Cohen's d, 0.28. CGI-S results aligned with MADRS results. In patients with minimal response to antidepressant treatment, the incidence of TEAEs was 196/328 (59.8%) for antidepressant + brexpiprazole and 160/335 (47.8%) for antidepressant + placebo. In patients with partial response to antidepressant treatment, corresponding values were 63/115 (54.8%) and 49/120 (40.8%).

Conclusions and relevance: Adjunctive brexpiprazole may be efficacious in MDD regardless of whether patients show minimal or partial response to antidepressant treatment.

Trial registration: Post hoc analysis of NCT01360645, NCT01360632, NCT02196506 (ClinicalTrials.gov).

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
8.40
自引率
2.10%
发文量
230
审稿时长
4-8 weeks
期刊介绍: The central focus of the journal is on research that advances understanding of existing and new neuropsychopharmacological agents including their mode of action and clinical application or provides insights into the biological basis of psychiatric disorders and thereby advances their pharmacological treatment. Such research may derive from the full spectrum of biological and psychological fields of inquiry encompassing classical and novel techniques in neuropsychopharmacology as well as strategies such as neuroimaging, genetics, psychoneuroendocrinology and neuropsychology.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信