Inoue Takeshi, Fujimoto Shinji, Marumoto Tatsuro, Kitagawa Tadayuki, Ishida Kazuyuki, Nakajima Tadashi, Moriguchi Yoshiya, Fujikawa Keita, Watanabe Koichiro
Department of Psychiatry, Tokyo Medical University, Tokyo, Japan.
Japan Medical Office, Takeda Pharmaceutical Co., Ltd, Tokyo, Japan.
Neuropsychiatr Dis Treat. 2021 Dec 18;17:3735-3741. doi: 10.2147/NDT.S340309. eCollection 2021.
Several weeks of treatment with an antidepressive agent may be required before efficacy is demonstrated in patients with major depressive disorder. This study investigated the predictive value of early partial improvement with vortioxetine for treatment response and remission.
This was a post hoc analysis of an 8-week, randomized, double-blind, placebo-controlled, Phase 3 study of vortioxetine (10 mg or 20 mg) in Japanese patients aged 20-75 years with recurrent major depressive disorder and a Montgomery-Åsberg Depression Rating Scale (MADRS) score of at least 26. The key outcomes were the predictive value of early partial improvement (reduction in MADRS total score of ≥20% from baseline to week 2) with vortioxetine for MADRS response (≥50% decrease in score from baseline) and remission (decrease in score to ≤10) at week 8.
Relevant data were available for 478 patients; 62/158 patients receiving placebo, 71/162 receiving vortioxetine 10 mg, and 66/158 receiving vortioxetine 20 mg were early improvers. Early improvers receiving vortioxetine (10 mg or 20 mg) were more likely than non-early improvers to achieve a week 8 response (71.2-73.2% vs 29.7-38.0%) or remission (50.7-51.5% vs 17.4-18.7%). Positive predictive values for response and remission with vortioxetine were ~70% and ~50%, respectively; negative predictive values were ~70% and ~80%, respectively.
Improvement with vortioxetine may be predicted by early partial improvement in MADRS score. Some patients may benefit from longer-term treatment even without early improvement, another finding that may aid clinical decision-making. ClinicalTrials.gov registration for primary study: NCT02389816.
对于重度抑郁症患者,可能需要数周的抗抑郁药治疗才能显示出疗效。本研究调查了伏硫西汀早期部分改善对治疗反应和缓解的预测价值。
这是一项事后分析,该研究为一项为期8周、随机、双盲、安慰剂对照的3期研究,研究对象为年龄在20 - 75岁、患有复发性重度抑郁症且蒙哥马利-艾斯伯格抑郁量表(MADRS)评分至少为26的日本患者,给予伏硫西汀(10毫克或20毫克)治疗。主要结局是伏硫西汀早期部分改善(从基线到第2周MADRS总分降低≥20%)对第8周时MADRS反应(评分从基线降低≥50%)和缓解(评分降低至≤10)的预测价值。
478例患者有相关数据;158例接受安慰剂治疗的患者中有62例、162例接受10毫克伏硫西汀治疗的患者中有71例、158例接受20毫克伏硫西汀治疗的患者中有66例为早期改善者。接受伏硫西汀(10毫克或20毫克)治疗的早期改善者比非早期改善者更有可能在第8周实现反应(71.2 - 73.2%对29.7 - 38.0%)或缓解(50.7 - 51.5%对17.4 - 18.7%)。伏硫西汀对反应和缓解的阳性预测值分别约为70%和50%;阴性预测值分别约为70%和80%。
MADRS评分的早期部分改善可能预示伏硫西汀治疗有效。即使没有早期改善,一些患者可能从长期治疗中获益,这一发现也有助于临床决策。主要研究在ClinicalTrials.gov的注册号:NCT02389816。