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Adrenal suppression from vamorolone and prednisone in Duchenne muscular dystrophy: results from the phase 2b clinical trial.
Ahmet, Alexandra; Tobin, Rebecca; Dang, Utkarsh J; Rooman, Raoul; Guglieri, Michela; Clemens, Paula R; Hoffman, Eric P; Ward, Leanne M.
Afiliación
  • Ahmet A; Division of Endocrinology, Children's Hospital of Eastern Ontario and Department of Pediatrics, University of Ottawa, Ottawa, Ontario, Canada.
  • Tobin R; Children's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario, Canada.
  • Dang UJ; Carleton University, Ottawa, Ontario, Canada.
  • Rooman R; Carleton University, Ottawa, Ontario, Canada.
  • Guglieri M; PendoCon bv, Putte, Belgium.
  • Clemens PR; John Walton Muscular Dystrophy Research Centre, Newcastle University and Newcastle Hospital National Health Service Foundation Trust, Newcastle, UK.
  • Hoffman EP; University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, United States.
  • Ward LM; Binghamton University - State University of New York, Binghamton, New York, United States.
Article en En | MEDLINE | ID: mdl-39097643
ABSTRACT
CONTEXT Vamorolone, a novel "dissociative" steroid, demonstrated similar efficacy in muscle function relative to prednisone 0.75 mg/kg/day but improved linear growth and bone turnover markers in a randomized trial of pediatric Duchenne muscular dystrophy (DMD).

OBJECTIVES:

To determine the frequency of adrenal suppression (AS) induced by vamorolone and prednisone in pediatric DMD, and to assess cortisol thresholds using a monoclonal antibody immunoassay.

METHODS:

Post-hoc analysis of cortisol levels was performed on data from a randomized, double-blind, placebo- and prednisone-controlled 24-week trial of vamorolone with a 24-week crossover extension. Morning and ACTH-stimulated cortisol levels were measured using the Elecsys II immunoassay, with AS defined as a stimulated cortisol of <500nmol/L ("historical threshold") and <400nmol/L ("revised threshold").

RESULTS:

Mean age at enrolment was 5.41±0.86 years (N=118). At Week 24, proportion of participants with AS using the historical and revised cortisol thresholds, respectively, were as follows prednisone 0.75 mg/kg/day=100% (25/25) and 92.0% (23/25); vamorolone 6 mg/kg/day=95.2% (20/21) and 90.5% (19/21); vamorolone 2 mg/kg/day=84.2% (16/19) and 47.5% (9/19); and placebo=20.0% (4/20) and 0% (0/20). Morning and peak ACTH-stimulated cortisol were strongly correlated in steroid-treated boys (Spearman correlation week 48=0.83).

CONCLUSIONS:

AS after vamorolone and prednisone was frequent and vamorolone-associated AS appeared dose-dependent. A lower stimulated cortisol threshold may be appropriate when using a monoclonal assay. We recommend hydrocortisone for glucocorticoid stress dosing in patients receiving vamorolone.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Clin Endocrinol Metab Año: 2024 Tipo del documento: Article País de afiliación: Canadá

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Clin Endocrinol Metab Año: 2024 Tipo del documento: Article País de afiliación: Canadá