Tolerability of vortioxetine compared to selective serotonin reuptake inhibitors in older adults with major depressive disorder (VESPA): a randomised, assessor-blinded and statistician-blinded, multicentre, superiority trial.

Adverse events Major depressive disorder Older adults Serotonin selective reuptake inhibitors Tolerability Vortioxetine

Journal

EClinicalMedicine
ISSN: 2589-5370
Titre abrégé: EClinicalMedicine
Pays: England
ID NLM: 101733727

Informations de publication

Date de publication:
Mar 2024
Historique:
received: 21 09 2023
revised: 30 01 2024
accepted: 01 02 2024
medline: 22 2 2024
pubmed: 22 2 2024
entrez: 22 2 2024
Statut: epublish

Résumé

Major depressive disorder (MDD) is prevalent and disabling among older adults. Standing on its tolerability profile, vortioxetine might be a promising alternative to selective serotonin reuptake inhibitors (SSRIs) in such a vulnerable population. We conducted a randomised, assessor- and statistician-blinded, superiority trial including older adults with MDD. The study was conducted between 02/02/2019 and 02/22/2023 in 11 Italian Psychiatric Services. Participants were randomised to vortioxetine or one of the SSRIs, selected according to common practice. Treatment discontinuation due to adverse events after six months was the primary outcome, for which we aimed to detect a 12% difference in favour of vortioxetine. The study was registered in the online repository clinicaltrials.gov (NCT03779789). The intention-to-treat population included 179 individuals randomised to vortioxetine and 178 to SSRIs. Mean age was 73.7 years (standard deviation 6.1), and 264 participants (69%) were female. Of those on vortioxetine, 78 (44%) discontinued the treatment due to adverse events at six months, compared to 59 (33%) of those on SSRIs (odds ratio 1.56; 95% confidence interval 1.01-2.39). Adjusted and per-protocol analyses confirmed point estimates in favour of SSRIs, but without a significant difference. With the exception of the unadjusted survival analysis showing SSRIs to outperform vortioxetine, secondary outcomes provided results consistent with a lack of substantial safety and tolerability differences between the two arms. Overall, no significant differences emerged in terms of response rates, depressive symptoms and quality of life, while SSRIs outperformed vortioxetine in terms of cognitive performance. As opposed to what was previously hypothesised, vortioxetine did not show a better tolerability profile compared to SSRIs in older adults with MDD in this study. Additionally, hypothetical advantages of vortioxetine on depression-related cognitive symptoms might be questioned. The study's statistical power and highly pragmatic design allow for generalisability to real-world practice. The study was funded by the Italian Medicines Agency within the "2016 Call for Independent Drug Research".

Sections du résumé

Background UNASSIGNED
Major depressive disorder (MDD) is prevalent and disabling among older adults. Standing on its tolerability profile, vortioxetine might be a promising alternative to selective serotonin reuptake inhibitors (SSRIs) in such a vulnerable population.
Methods UNASSIGNED
We conducted a randomised, assessor- and statistician-blinded, superiority trial including older adults with MDD. The study was conducted between 02/02/2019 and 02/22/2023 in 11 Italian Psychiatric Services. Participants were randomised to vortioxetine or one of the SSRIs, selected according to common practice. Treatment discontinuation due to adverse events after six months was the primary outcome, for which we aimed to detect a 12% difference in favour of vortioxetine. The study was registered in the online repository clinicaltrials.gov (NCT03779789).
Findings UNASSIGNED
The intention-to-treat population included 179 individuals randomised to vortioxetine and 178 to SSRIs. Mean age was 73.7 years (standard deviation 6.1), and 264 participants (69%) were female. Of those on vortioxetine, 78 (44%) discontinued the treatment due to adverse events at six months, compared to 59 (33%) of those on SSRIs (odds ratio 1.56; 95% confidence interval 1.01-2.39). Adjusted and per-protocol analyses confirmed point estimates in favour of SSRIs, but without a significant difference. With the exception of the unadjusted survival analysis showing SSRIs to outperform vortioxetine, secondary outcomes provided results consistent with a lack of substantial safety and tolerability differences between the two arms. Overall, no significant differences emerged in terms of response rates, depressive symptoms and quality of life, while SSRIs outperformed vortioxetine in terms of cognitive performance.
Interpretation UNASSIGNED
As opposed to what was previously hypothesised, vortioxetine did not show a better tolerability profile compared to SSRIs in older adults with MDD in this study. Additionally, hypothetical advantages of vortioxetine on depression-related cognitive symptoms might be questioned. The study's statistical power and highly pragmatic design allow for generalisability to real-world practice.
Funding UNASSIGNED
The study was funded by the Italian Medicines Agency within the "2016 Call for Independent Drug Research".

Identifiants

pubmed: 38384338
doi: 10.1016/j.eclinm.2024.102491
pii: S2589-5370(24)00070-1
pmc: PMC10879669
doi:

Banques de données

ClinicalTrials.gov
['NCT03779789']

Types de publication

Journal Article

Langues

eng

Pagination

102491

Investigateurs

Eugenio Aguglia (E)
Andrea Aguglia (A)
Maria Chiara Alessi (MC)
Gabriele Avincola (G)
Bianca Bachi (B)
Angelo Barbato (A)
Corrado Barbui (C)
Francesco Bartoli (F)
Gianna Bernasconi (G)
Andrea Birgillito (A)
Emanuele Bisso (E)
Stefano Bonora (S)
Angela Calabrese (A)
Camilla Callegari (C)
Tommaso Callovini (T)
Aurelia Canestro (A)
Salvo Canonico (S)
Chiara Alessandro Capogrosso (CA)
Elvira Carbone (E)
Doriana Carosielli (D)
Giuseppe Carrà (G)
Massimo Cartabia (M)
Ivano Caselli (I)
Daniele Cavaleri (D)
Simone Cavallotti (S)
Clara Cavallotto (C)
Marco Cesca (M)
Cecilia Chiarenza (C)
Riccardo Matteo Cioni (RM)
Sara Coloccini (S)
Marco Cruciata (M)
Claudia Cumerlato (C)
Armando D'Agostino (A)
Barbara D'Avanzo (B)
Pasquale De Fazio (P)
Renato De Filippis (R)
Manuela De Palma (M)
Sasha Del Vecchio (S)
Bianca Della Rocca (B)
Chiara Di Natale (C)
Ettore D'Onofrio (E)
Irene Espa (I)
Giulia Fior (G)
Marta Gancitano (M)
Matteo Gari (M)
Chiara Gastaldon (C)
Barbara Giordano (B)
Laura Giusti (L)
Luigi Grassi (L)
Pierluca Guzzi (P)
Marta Ielmini (M)
Gianmarco Ingrosso (G)
Celeste Isella (C)
Annamaria Lax (A)
Silvia Mammarella (S)
Leonardo Marano (L)
Federico Marconi (F)
Marco Marella (M)
Alessia Metelli (A)
Giulia Michencig (G)
Andrea Miuli (A)
Alessandro Moncada (A)
Igor Monti (I)
Pietro Morello (P)
Federico Moretti (F)
Marco Morreale (M)
Alessio Mosca (A)
Christian Nasti (C)
Michela Nosé (M)
Filippo Ogheri (F)
Margherita Oresti (M)
Alessandra Ornaghi (A)
Giovanni Ostuzzi (G)
Dario Palpella (D)
Corinna Pancheri (C)
Davide Papola (D)
Silvia Passeri (S)
Mauro Pettorusso (M)
Susanna Piacenti (S)
Irene Pinucci (I)
Valentina Pugliese (V)
Marianna Purgato (M)
Marianna Rania (M)
Federica Robbi (F)
Alessandro Rodolico (A)
Samantha Romito (S)
Barbara Ronchi (B)
Rita Roncone (R)
Valentina Roselli (V)
Cristina Segura-Garcia (C)
Maria Salvina Signorelli (MS)
Gabriele Simonelli (G)
Antonella Sociali (A)
Enrico Sterzi (E)
Serena Sturiale (S)
Antonio Tambelli (A)
Mauro Tettamanti (M)
Beatrice Todesco (B)
Alice Trabucco (A)
Giulia Turrini (G)
Veronica Villa (V)
Federico Wiedenmann (F)
Luca Zambuto (L)
Elisa Zanini (E)
Chiara Zannini (C)
Luigi Zerbinati (L)

Informations de copyright

© 2024 The Author(s).

Déclaration de conflit d'intérêts

A. A. received honoraria for presentations from Lundbeck, Viatris, Angelini. E. A. received research grants, consulting fees and honoraria for presentations from Allergan, Angelini, Doc Generici, FB-Health, Janssen-Cilag, Lundbeck, Otsuka, Fidia, Recordati. E. A. C. received support for attending meetings from Janssen-Cilag. F. B. received consulting fees and support for attending meetings from Angelini, Janssen-Cilag, Otsuka. G.M. received research grants, consulting fees and honoraria for presentations from Angelini, Doc Generici, Janssen-Cilag, Lundbeck, Neuraxpharm, Otsuka, Pfizer, Servier, Rovi, Recordati. R. d. F. received consulting fees and honoraria for presentations from Janssen-Cilag, and support for attending meetings from Janssen-Cilag and ROVI. All the other authors have no competing interests to disclose.

Auteurs

Giovanni Ostuzzi (G)

Department of Neuroscience, Biomedicine and Movement Sciences, Section of Psychiatry, University of Verona, Verona, Italy.

Chiara Gastaldon (C)

Department of Neuroscience, Biomedicine and Movement Sciences, Section of Psychiatry, University of Verona, Verona, Italy.
Institute for Social and Preventive Medicine, University of Bern, Bern, Switzerland.

Mauro Tettamanti (M)

Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milano, Italy.

Massimo Cartabia (M)

Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milano, Italy.

Igor Monti (I)

Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milano, Italy.

Andrea Aguglia (A)

Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DiNOGMI), Section of Psychiatry, University of Genoa, Genoa, Italy.
IRCCS Ospedale Policlinico San Martino, Genoa, Italy.

Eugenio Aguglia (E)

Department of Clinical and Experimental Medicine, Institute of Psychiatry, University of Catania, Catania, Italy.

Francesco Bartoli (F)

Department of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy.

Camilla Callegari (C)

Department of Medicine and Surgery, Section of Psychiatry, University of Insubria, Varese, Italy.

Andrea Canozzi (A)

Department of Neuroscience, Biomedicine and Movement Sciences, Section of Psychiatry, University of Verona, Verona, Italy.

Elvira Anna Carbone (EA)

Psychiatry Unit, Department of Health Sciences, University Magna Graecia of Catanzaro, Catanzaro, Italy.
Psychiatry Unit, Department of Medical and Surgical Sciences, University Magna Graecia of Catanzaro, Catanzaro, Italy.
Outpatient Clinic for Clinical Research and Treatment of Eating Disorders, University Hospital Renato Dulbecco, Catanzaro, Italy.

Giuseppe Carrà (G)

Department of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy.

Rosangela Caruso (R)

Department of Neuroscience and Rehabilitation, Institute of Psychiatry, University of Ferrara, Ferrara, Italy.
University Hospital Psychiatry Unit, Integrated Department of Mental Health and Addictive Behavior, University S. Anna Hospital and Health Trust, Ferrara, Italy.

Simone Cavallotti (S)

Department of Mental Health and Addiction, ASST Santi Paolo e Carlo, Milan, Italy.
Department of Health Sciences, Università degli Studi di Milano, Milan, Italy.

Stefania Chiappini (S)

Department of Neurosciences, Imaging and Clinical Sciences, University "G. D'Annunzio", Chieti, Italy.

Fabrizio Colasante (F)

Department of Neuroscience, Biomedicine and Movement Sciences, Section of Psychiatry, University of Verona, Verona, Italy.
Santa Chiara Hospital, Verona, Italy.

Beatrice Compri (B)

Department of Neuroscience, Biomedicine and Movement Sciences, Section of Psychiatry, University of Verona, Verona, Italy.

Armando D'Agostino (A)

Department of Mental Health and Addiction, ASST Santi Paolo e Carlo, Milan, Italy.
Department of Health Sciences, Università degli Studi di Milano, Milan, Italy.

Pasquale De Fazio (P)

Psychiatry Unit, Department of Health Sciences, University Magna Graecia of Catanzaro, Catanzaro, Italy.
Psychiatry Unit, Department of Medical and Surgical Sciences, University Magna Graecia of Catanzaro, Catanzaro, Italy.
Outpatient Clinic for Clinical Research and Treatment of Eating Disorders, University Hospital Renato Dulbecco, Catanzaro, Italy.

Renato de Filippis (R)

Psychiatry Unit, Department of Health Sciences, University Magna Graecia of Catanzaro, Catanzaro, Italy.
Psychiatry Unit, Department of Medical and Surgical Sciences, University Magna Graecia of Catanzaro, Catanzaro, Italy.
Outpatient Clinic for Clinical Research and Treatment of Eating Disorders, University Hospital Renato Dulbecco, Catanzaro, Italy.

Matteo Gari (M)

IRCCS Ospedale Policlinico San Martino, Genoa, Italy.

Marta Ielmini (M)

Department of Medicine and Surgery, Section of Psychiatry, University of Insubria, Varese, Italy.

Gianmarco Ingrosso (G)

Department of Mental Health and Addiction, ASST Santi Paolo e Carlo, Milan, Italy.
Department of Health Sciences, Università degli Studi di Milano, Milan, Italy.

Silvia Mammarella (S)

Department of Life, Health and Environmental Sciences, University of L'Aquila, L'Aquila, Italy.

Giovanni Martinotti (G)

Department of Neurosciences, Imaging and Clinical Sciences, University "G. D'Annunzio", Chieti, Italy.

Alessandro Rodolico (A)

Department of Clinical and Experimental Medicine, Institute of Psychiatry, University of Catania, Catania, Italy.

Rita Roncone (R)

Department of Life, Health and Environmental Sciences, University of L'Aquila, L'Aquila, Italy.

Enrico Sterzi (E)

Pharmacy Unit, Azienda Ospedaliera Universitaria Integrata di Verona, Verona, Italy.

Lorenzo Tarsitani (L)

Department of Human Neurosciences, Sapienza University of Rome, Rome, Italy.

Elisa Tiberto (E)

Department of Neuroscience and Rehabilitation, Institute of Psychiatry, University of Ferrara, Ferrara, Italy.
University Hospital Psychiatry Unit, Integrated Department of Mental Health and Addictive Behavior, University S. Anna Hospital and Health Trust, Ferrara, Italy.

Liliana Todini (L)

Department of Human Neurosciences, Sapienza University of Rome, Rome, Italy.

Francesco Amaddeo (F)

Department of Neuroscience, Biomedicine and Movement Sciences, Section of Psychiatry, University of Verona, Verona, Italy.

Barbara D'Avanzo (B)

Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milano, Italy.

Angelo Barbato (A)

Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milano, Italy.

Corrado Barbui (C)

Department of Neuroscience, Biomedicine and Movement Sciences, Section of Psychiatry, University of Verona, Verona, Italy.

Classifications MeSH