Morrens Joachim, Mathews Maju, Popova Vanina, Borentain Stephane, Rive Benoit, Gonzalez Martin Moro Beatriz, Jamieson Carol, Zhang Qiaoyi
Janssen Research & Development, Beerse, Belgium.
Janssen Global Services, LLC, Titusville, NJ, USA.
Neuropsychiatr Dis Treat. 2022 Jun 7;18:1127-1132. doi: 10.2147/NDT.S358367. eCollection 2022.
BACKGROUND: This post-hoc analysis evaluated the agreement between Clinical Global Impressions-Severity (CGI-S) score- and Montgomery-Åsberg Depression Rating Scale (MADRS) total score-based assessment of response in patients with treatment-resistant depression (TRD) treated with esketamine nasal spray plus a newly initiated oral antidepressant (ESK-NS + AD). METHODS: Data were analyzed from a phase 3, randomized, double-blind study (TRANSFORM-2) of flexibly dosed esketamine or placebo nasal spray plus a newly initiated oral-AD in adults with moderate-to-severe TRD. Patients with ≥50% reduction in MADRS from baseline at the end of the 4-week acute treatment phase were defined as responders. For the CGI-S-based assessment of response, patients with ≥2 points decrease from baseline or a CGI-S score of ≤3 (mildly depressed to normal) were considered responders. Cohen's kappa coefficient was calculated to assess level of agreement between MADRS and CGI-S-based assessments. RESULTS: At the end of 4-week treatment, the proportion of responders among all study patients (n=201) was similar when assessed using the MADRS (61%) and CGI-S (62%) methods, with substantial agreement (Cohen's kappa=0.76; sensitivity=92%; specificity=84%) between both methods. When restricting analysis to ESK-NS + AD-treated patients (n=101) who had a higher response rate (on MADRS: 69%; on CGI-S: 68%), the agreement remained substantial (Cohen's kappa=0.75; sensitivity=91%; specificity=84%). CONCLUSION: The CGI-S may be a practical and reliable alternative to the MADRS to assess response to ESK-NS + AD in patients with TRD and can be used in real-world practice to support informed treatment decisions.
背景:本事后分析评估了在难治性抑郁症(TRD)患者中,使用艾氯胺酮鼻喷雾剂加新启用的口服抗抑郁药(ESK-NS + AD)治疗时,基于临床总体印象-严重程度(CGI-S)评分和蒙哥马利-艾斯伯格抑郁量表(MADRS)总分的疗效评估之间的一致性。 方法:对一项3期随机双盲研究(TRANSFORM-2)的数据进行分析,该研究中,中度至重度TRD成人患者接受灵活剂量的艾氯胺酮或安慰剂鼻喷雾剂加新启用的口服抗抑郁药治疗。在4周急性治疗期结束时,MADRS较基线降低≥50%的患者被定义为有反应者。对于基于CGI-S的疗效评估,较基线降低≥2分或CGI-S评分为≤3(轻度抑郁至正常)的患者被视为有反应者。计算Cohen's kappa系数以评估基于MADRS和CGI-S的评估之间的一致性水平。 结果:在4周治疗结束时,使用MADRS(61%)和CGI-S(62%)方法评估时,所有研究患者(n = 201)中有反应者的比例相似,两种方法之间具有高度一致性(Cohen's kappa = 0.76;敏感性 = 92%;特异性 = 84%)。当将分析限制在反应率较高的ESK-NS + AD治疗患者(n = 101)时(基于MADRS:69%;基于CGI-S:68%),一致性仍然很高(Cohen's kappa = 0.75;敏感性 = 91%;特异性 = 84%)。 结论:对于评估TRD患者对ESK-NS + AD的反应,CGI-S可能是MADRS的一种实用且可靠的替代方法,可用于实际临床实践以支持明智的治疗决策。
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