Predicting efficacy of viloxazine extended-release treatment in adults with ADHD using an early change in ADHD symptoms: Machine learning Post Hoc analysis of a phase 3 clinical trial.


Journal

Psychiatry research
ISSN: 1872-7123
Titre abrégé: Psychiatry Res
Pays: Ireland
ID NLM: 7911385

Informations de publication

Date de publication:
12 2022
Historique:
received: 07 07 2022
accepted: 22 10 2022
pubmed: 15 11 2022
medline: 3 12 2022
entrez: 14 11 2022
Statut: ppublish

Résumé

Early response to viloxazine extended-release (viloxazine ER, Qelbree®) treatment predicted efficacy outcome in pediatric subjects with attention-deficit/hyperactivity disorder (ADHD). This study sought to determine whether the machine learning lasso model used in the pediatric study would predict response to viloxazine ER in an adult population based on early improvements in ADHD symptoms. We used data from a double-blind, placebo-controlled, flexible-dose (200-600 mg) study of viloxazine ER (N = 354; 18 to 60 years old). Area under the Receiver Operating Characteristic Curve (ROC AUC) statistics were computed using the lasso model from pediatric data to predict responder status in adults. Response was defined as ≥50% reduction from baseline in the Adult ADHD Investigator Symptoms Rating Scale (AISRS) Total score at Week 6. The adult study sample included 127 viloxazine ER-treated subjects with Week 6 data. Fifty-one subjects (40.2%) were categorized as responders. The ROC curves indicated that data collected up to Week 2 were sufficient to accurately predict treatment response at Week 6 with 68% positive predictive power, 80% sensitivity, and 74% specificity. This analysis demonstrated that the predictive model estimated from the child data generalizes to adults with ADHD, further supporting the consistency of viloxazine ER treatment across age groups.

Identifiants

pubmed: 36375329
pii: S0165-1781(22)00513-3
doi: 10.1016/j.psychres.2022.114922
pii:
doi:

Substances chimiques

Central Nervous System Stimulants 0
Delayed-Action Preparations 0
Viloxazine 5I5Y2789ZF

Types de publication

Clinical Trial, Phase III Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

114922

Informations de copyright

Copyright © 2022 The Authors. Published by Elsevier B.V. All rights reserved.

Auteurs

Stephen V Faraone (SV)

Departments of Psychiatry and of Neuroscience and Physiology, SUNY Upstate Medical University, Syracuse, NY, USA.

Roberto Gomeni (R)

Pharmacometrica, Lieu-dit Longcol, La Fouillade, France.

Joseph T Hull (JT)

Supernus Pharmaceuticals, Inc., Rockville, MD, USA.

Soumya A Chaturvedi (SA)

Supernus Pharmaceuticals, Inc., Rockville, MD, USA.

Gregory D Busse (GD)

Supernus Pharmaceuticals, Inc., Rockville, MD, USA.

Zare Melyan (Z)

Supernus Pharmaceuticals, Inc., Rockville, MD, USA.

Welton O'Neal (W)

Supernus Pharmaceuticals, Inc., Rockville, MD, USA.

Jonathan Rubin (J)

Supernus Pharmaceuticals, Inc., Rockville, MD, USA.

Azmi Nasser (A)

Supernus Pharmaceuticals, Inc., Rockville, MD, USA. Electronic address: anasser@supernus.com.

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Classifications MeSH