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http://hdl.handle.net/10362/161171| Título: | ICEBERG study |
| Autor: | Oliveira-Maia, AJ Morrens, Joachim Rive, Benoit Godinov, Yordan Cabrieto, Jedelyn Perualila, Nolen Barbreau, Sebastien Mulhern-Haughey, Siobhán |
| Palavras-chave: | esketamine nasal spray indirect comparison real-world evidence remission response treatment resistant depression Psychiatry and Mental health SDG 3 - Good Health and Well-being |
| Data: | 2023 |
| Resumo: | Background: Treatment resistant depression (TRD) affects 10–30% of patients with major depressive disorder. In 4-week trials, esketamine nasal spray (NS) was efficacious vs. placebo when both were initiated in addition to a new selective serotonin or serotonin norepinephrine reuptake inhibitor. However, comparison with an extended range of real-world treatments (RWT) is lacking. Methods: ICEBERG was an adjusted indirect treatment comparison using propensity score-based inverse probability weighting, performed on 6-month response and remission data from patients receiving esketamine NS plus oral antidepressant from the SUSTAIN-2 (NCT02497287; clinicaltrials.gov) study, compared with patients receiving other RWT from the European Observational TRD Cohort (EOTC; NCT03373253; clinicaltrials.gov) study. SUSTAIN-2 was a long-term open-label study of esketamine NS, while the EOTC was conducted at a time when esketamine NS was not available as RWT. Threshold and sensitivity analyses were conducted to assess how robust the primary analyses were. Results: Patients receiving esketamine NS had a higher probability of 6-month response (49.7% [95% confidence interval (CI) 45.6–53.9]) and remission (33.6% [95% CI 29.7–37.6]) vs. patients receiving RWT (26.4% [95% CI 21.5–31.4] and 18.2% [95% CI 13.9–22.5], respectively), according to rescaled average treatment effect among treated estimates. Resulting adjusted odds ratios (OR) and relative risk (RR) favoured esketamine NS over RWT for 6-month response (OR 2.756 [95% CI 2.034–3.733], p < 0.0001; RR 1.882 [95% CI 1.534–2.310], p < 0.0001) and remission (OR 2.276 [95% CI 1.621–3.196], p < 0.0001; RR 1.847 [95% CI 1.418–2.406], p < 0.0001). Threshold analyses suggested that differences between the two studies were robust, and results were consistent across extensive sensitivity analyses. Conclusion: ICEBERG supports that, at 6 months, esketamine NS has a substantial and significant benefit over RWT for patients with TRD. While results may be affected by unobserved confounding factors, threshold analyses suggested these were unlikely to impact the study conclusions. To view an animated summary of this publication, please click on the Supplementary video. |
| Descrição: | Funding Information: AJOM received grants from Trials sponsored by Schuhfried GmBH, Janssen and Compass Pathways, Ltd.; received payment or honoraria from MSD, Neurolite AG, Janssen, and the European Monitoring Centre for Drugs and Drug Addiction; participated in advisory boards for Janssen and Angelini; investigator-driven research funded by Fundação para Ciência e Tecnologia (PTDC/MED-NEU/31331/2017; PTDC/SAU-NUT/3507/2021; PTDC/MED-NEU/1552/2021), Fundação para Ciência e Tecnologia and FEDER (FCT-PTDC/MEC-PSQ/30302/2017-IC&DTLISBOA-01-0145-FEDER-030845; PTDC/MEC-PSQ/30302/2017_LISBOA-01-0145-FEDER-30302), the European Commission Horizon 2020 program (H2020-SC1-2017-CNECT-2-777167-ΒΟUNCE; H2020-SC1-DTH-2019-875358-FAITH), the European Joint Programme in Rare Diseases (Joint Translational Call 2019) through Fundação para Ciência e Tecnologia (EJPRD/0001/2020) and the European Research Council (grant agreement 950357). JM is a former employee of Janssen EMEA and current employee of AbbVie. BR, YG, JC, NP, SB, and SMH are employees of Janssen EMEA. Funding Information: The authors declare that this study was sponsored by Janssen EMEA. The funder had the following involvement in the study: this article was based on the original studies NCT02497287 and 54135419DEP4001, both also sponsored by Janssen EMEA. Support for third-party writing assistance for this article, provided by Laura Mawdsley, Tim Jones, and Julia Stevens, Costello Medical, UK, was funded by Janssen EMEA in accordance with Good Publication Practice (GPP3) guidelines (http://www.ismpp.org/gpp3). Publisher Copyright: Copyright © 2023 Oliveira-Maia, Morrens, Rive, Godinov, Cabrieto, Perualila, Barbreau and Mulhern-Haughey. |
| Peer review: | yes |
| URI: | http://hdl.handle.net/10362/161171 |
| DOI: | https://doi.org/10.3389/fpsyt.2023.1250980 |
| ISSN: | 1664-0640 |
| Aparece nas colecções: | NMS - Artigos em revista internacional com arbitragem científica |
Ficheiros deste registo:
| Ficheiro | Descrição | Tamanho | Formato | |
|---|---|---|---|---|
| fpsyt_14_1250980.pdf | 1,48 MB | Adobe PDF | Ver/Abrir |
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