Sackeim Harold A, Conway Charles R, Aaronson Scott T, Bunker Mark T, Gordon Charles, Lee Ying-Chieh Lisa, Shy Olivia, Majewski Shannon, Tran Quyen, Rush A John
Department of Psychiatry and Behavioral Sciences, Medical University of South Carolina, Charleston, SC, USA.
Department of Psychiatry, Washington University in St. Louis, St. Louis, MO, USA.
J Affect Disord. 2025 Jul 1;380:135-145. doi: 10.1016/j.jad.2025.03.124. Epub 2025 Mar 22.
The RECOVER trial randomized 493 patients with markedly treatment-resistant major depressive disorder to treatment-as-usual with or without active vagus nerve stimulation (VNS Therapy). While the primary outcome measure did not statistically separate the treatment conditions, the field may lack optimal metrics for quantifying symptom improvement in markedly treatment-resistant patients.
This study examined the impact of three factors on sensitivity to clinical improvement across the total RECOVER sample and to differences in the effectiveness of the randomized conditions, systematically varying outcome classification (remission, response, and partial response), observation period (3-12 months, 6-12 months, 10-12 months and last observation), and depression rating scale.
Effect sizes for detecting therapeutic change across the total sample and the difference in effectiveness between the randomized groups were markedly higher for partial response than response or remission classifications. Longer observation periods produced larger therapeutic effects across the sample, but the effect sizes for the randomized treatment differences were substantially higher in the final 10-12 month period. The MADRS showed the least sensitivity to change across the sample and between the treatment groups. Using the partial response classification and the 10-12 month observation period, a significant difference between the groups was obtained for 3 of 4 depression scales.
The findings derive from a retrospective assessment of alternative outcome metrics.
In a large randomized controlled trial of VNS for markedly treatment-resistant depression, the magnitude of therapeutic effects and separation of treatment groups differed as a function of outcome classification, measurement period, and rating scale.
RECOVER试验将493例对治疗有明显抵抗的重度抑郁症患者随机分为接受常规治疗或常规治疗联合主动迷走神经刺激(VNS治疗)两组。虽然主要结局指标在统计学上未区分治疗组,但该领域可能缺乏用于量化对治疗有明显抵抗的患者症状改善情况的最佳指标。
本研究考察了三个因素对整个RECOVER样本临床改善敏感性以及随机分组条件有效性差异的影响,系统地改变结局分类(缓解、有效和部分有效)、观察期(3至12个月、6至12个月、10至12个月以及末次观察)和抑郁评定量表。
对于整个样本,检测治疗变化的效应量以及随机分组之间的有效性差异,部分有效分类的效应量显著高于有效或缓解分类。更长的观察期在整个样本中产生了更大的治疗效果,但在最后10至12个月期间,随机治疗差异的效应量显著更高。蒙哥马利-艾森伯格抑郁量表(MADRS)在整个样本以及治疗组之间对变化的敏感性最低。采用部分有效分类和10至12个月观察期,4个抑郁量表中有3个量表显示两组之间存在显著差异。
本研究结果来自对替代结局指标的回顾性评估。
在一项针对对治疗有明显抵抗的抑郁症患者的大型随机对照VNS试验中,治疗效果的大小以及治疗组之间的区分因结局分类、测量期和评定量表而异。