This secondary analysis of an open-label, single-blind, Phase IIIb trial (n=676) compares esketamine nasal spray plus an SSRI/SNRI versus extended-release quetiapine plus an SSRI/SNRI for treatment-resistant depression (TRD). It finds esketamine to be superior in achieving remission at week 8 (27.1% vs. 17.6%, p=0.003) and preventing relapse through week 32 (21.7% vs. 14.1%). Adverse events align with known safety profiles.
Abstract of Esketamine nasal spray versus quetiapine XR in adults with treatment-resistant depression
“Background In treatment-resistant depression, commonly defined as a lack of response to two or more consecutive treatments during the current depressive episode, the percentage of patients with remission is low and the percentage with relapse is high. The efficacy and safety of esketamine nasal spray as compared with extended-release quetiapine augmentation therapy, both in combination with ongoing treatment with a selective serotonin reuptake inhibitor (SSRI) or a serotonin–norepinephrine reuptake inhibitor (SNRI), in patients with treatment-resistant depression are unknown.
Methods In an open-label, single-blind (with raters unaware of group assignments), multicenter, phase 3b, randomized, active-controlled trial, we assigned patients, in a 1:1 ratio, to receive flexible doses (according to the summary of product characteristics) of esketamine nasal spray (esketamine group) or extended-release quetiapine (quetiapine group), both in combination with an SSRI or SNRI. The primary end point was remission, defined as a score of 10 or less on the Montgomery–Åsberg Depression Rating Scale (MADRS), at week 8 (scores range from 0 to 60, with higher scores indicating more severe depression). The key secondary end point was no relapse through week 32 after remission at week 8. All patients were included in the analysis; patients who discontinued the trial treatment were considered as having had an unfavorable outcome (i.e., they were grouped with patients who did not have remission or who had a relapse). Analyses of the primary and key secondary end points were adjusted for age and number of treatment failures.
Results Overall, 336 patients were assigned to the esketamine group and 340 to the quetiapine group. More patients in the esketamine group than in the quetiapine group had remission at week 8 (91 of 336 patients [27.1%] vs. 60 of 340 patients [17.6%]; P = 0.003) and had no relapse through week 32 after remission at week 8 (73 of 336 patients [21.7%] vs. 48 of 340 patients [14.1%]). Over 32 weeks of follow-up, the percentage of patients with remission, the percentage of patients with a treatment response, and the change in the MADRS score from baseline favored esketamine nasal spray. The adverse events were consistent with the established safety profiles of the trial treatments.
Conclusions In patients with treatment-resistant depression, esketamine nasal spray plus an SSRI or SNRI was superior to extended-release quetiapine plus an SSRI or SNRI with respect to remission at week 8.”
Authors: Roger S. McIntyre, Gregory Mattingly, Yordan Godinov, Jozefine Buyze, Ibrahim Turkoz, Patricia Cabrera, Manish Patel, Larry Martinez, Mai Himedan & Oliver Lopena
Summary of Esketamine nasal spray versus quetiapine XR in adults with treatment-resistant depression
The primary objective in treating major depressive disorder (MDD) is achieving remission, followed by maintenance therapy to prevent relapse. However, up to two-thirds of patients with MDD do not achieve remission with their first antidepressant treatment, and many who require multiple treatment attempts relapse within a year. Treatment-resistant depression (TRD) is commonly defined as the failure to respond to two or more antidepressant treatments administered at adequate doses and for an appropriate duration within a single depressive episode. TRD affects approximately 10% to 30% of individuals diagnosed with MDD and is associated with increased hospitalisations, higher rates of comorbid conditions, elevated mortality and suicide risk, and significant economic burden.
Pharmacological options for TRD include oral antidepressants and augmentation strategies, such as antipsychotics. Extended-release quetiapine is a widely used and guideline-supported augmentation agent for TRD. Esketamine nasal spray, in combination with a selective serotonin reuptake inhibitor (SSRI) or serotonin–norepinephrine reuptake inhibitor (SNRI), is currently the only approved treatment for TRD in Europe. Prior studies have shown that esketamine nasal spray reduces depressive symptoms and lowers relapse risk compared to placebo when combined with a newly initiated SSRI or SNRI. However, direct comparative data between esketamine and an established augmentation strategy, such as quetiapine, remains limited.
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https://doi.org/10.1017/s1092852924002451
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Cite this paper (APA)
McIntyre, R. S., Mattingly, G., Godinov, Y., Buyze, J., Turkoz, I., Cabrera, P., ... & Lopena, O. Esketamine nasal spray versus quetiapine XR in adults with treatment-resistant depression: a secondary analysis of the ESCAPE-TRD randomized clinical trial. CNS spectrums, 1-30.
Study details
Compounds studied
Ketamine
Topics studied
Depression
Treatment-Resistant Depression
Study characteristics
Active Placebo
Single-Blind
Open-Label
Randomized
Re-analysis
Participants
776
Humans
Institutes
Institutes associated with this publication
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Linked Clinical Trial
A Long-term Comparison of Esketamine Nasal Spray Versus Quetiapine Extended Release, Both in Combination With a Selective Serotonin Reuptake Inhibitor/Serotonin-Norepinephrine Reuptake Inhibitor, in Participants With Treatment Resistant Major Depressive Disorder (ESCAPE-TRD)This Phase III interventional trial (n=676) will evaluate the efficacy of flexibly dosed esketamine nasal spray compared with quetiapine extended-release (XR), both in combination with a continuing selective serotonin reuptake inhibitor/serotonin-norepinephrine reuptake inhibitor (SSRI/SNRI), in achieving remission in participants with treatment-resistant major depressive disorder (MDD) experiencing a moderate to severe depressive episode.