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Quality of life improvements following one year of setmelanotide in children and adult patients with Bardet-Biedl syndrome: phase 3 trial results.
Forsythe, Elizabeth; Haws, Robert M; Argente, Jesús; Beales, Philip; Martos-Moreno, Gabriel Á; Dollfus, Hélène; Chirila, Costel; Gnanasakthy, Ari; Buckley, Brieana C; Mallya, Usha G; Clément, Karine; Haqq, Andrea M.
Afiliación
  • Forsythe E; Genetics and Genomics Medicine Programme, University College London Great Ormond Street Institute of Child Health, London, UK.
  • Haws RM; Marshfield Clinic Research Institute, Marshfield, WI, USA.
  • Argente J; Department of Pediatrics and Pediatric Endocrinology, Universidad Autónoma de Madrid, University Hospital Niño Jesús, Madrid, Spain.
  • Beales P; CIBER "Fisiopatología de la Obesidad y Nutrición" (CIBEROBN), Instituto de Salud Carlos III, Madrid, Spain.
  • Martos-Moreno GÁ; IMDEA Food Institute, Madrid, Spain.
  • Dollfus H; Genetics and Genomics Medicine Programme, University College London Great Ormond Street Institute of Child Health, London, UK.
  • Chirila C; Department of Pediatrics and Pediatric Endocrinology, Universidad Autónoma de Madrid, University Hospital Niño Jesús, Madrid, Spain.
  • Gnanasakthy A; CIBER "Fisiopatología de la Obesidad y Nutrición" (CIBEROBN), Instituto de Salud Carlos III, Madrid, Spain.
  • Buckley BC; Hôpitaux Universitaires de Strasbourg, CARGO and Department of Medical Genetics, Strasbourg, France.
  • Mallya UG; RTI Health Solutions, Research Triangle Park, NC, USA.
  • Clément K; RTI Health Solutions, Research Triangle Park, NC, USA.
  • Haqq AM; Rhythm Pharmaceuticals, Inc., Boston, MA, USA.
Orphanet J Rare Dis ; 18(1): 12, 2023 01 16.
Article en En | MEDLINE | ID: mdl-36647077
ABSTRACT

BACKGROUND:

Bardet-Biedl syndrome is a rare genetic disease associated with hyperphagia and early-onset, severe obesity. There is limited evidence on how hyperphagia and obesity affect health-related quality of life in patients with Bardet-Biedl syndrome, and on how management of these symptoms may influence disease burden. This analysis evaluated changes in health-related quality of life in adults and children with Bardet-Biedl syndrome in a Phase 3 trial following 1 year of setmelanotide treatment (ClinicalTrials.gov identifier NCT03746522).

METHODS:

Patients with Bardet-Biedl syndrome and obesity received 52 weeks of treatment with setmelanotide and completed various self-reported health-related quality of life measures. Patients aged < 18 years or their caregiver completed the Pediatric Quality of Life Inventory (PedsQL; meaningful improvement, 4.4-point change); adults aged ≥ 18 years completed the Impact of Weight on Quality of Life Questionnaire-Lite (IWQOL-Lite; meaningful improvement range, 7.7-12-point change). Descriptive outcomes were reported in patients with data both at active treatment baseline and after 52 weeks of treatment.

RESULTS:

Twenty patients (< 18 years, n = 9; ≥ 18 years, n = 11) reported health-related quality of life at baseline and 52 weeks. For children and adolescents, PedsQL score mean change from baseline after 52 weeks was + 11.2; all patients with PedsQL impairment at baseline (n = 4) experienced clinically meaningful improvement. In adults, IWQOL-Lite score mean change from baseline was + 12.0. Of adults with IWQOL-Lite impairment at baseline (n = 8), 62.5% experienced clinically meaningful improvement. In adults, IWQOL-Lite score was significantly correlated with changes in percent body weight (P = 0.0037) and body mass index (P = 0.0098).

CONCLUSIONS:

After 1 year of setmelanotide, patients reported clinically meaningful improvements across multiple health-related quality of life measures. This study highlights the need to address the impaired health-related quality of life in Bardet-Biedl syndrome, and supports utility of setmelanotide for reducing this burden. Trial Registration NCT03746522. Registered November 19, 2018, https//clinicaltrials.gov/ct2/show/NCT03746522 .
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Calidad de Vida / Síndrome de Bardet-Biedl Tipo de estudio: Prognostic_studies Aspecto: Patient_preference Límite: Adolescent / Adult / Child / Humans Idioma: En Revista: Orphanet J Rare Dis Asunto de la revista: MEDICINA Año: 2023 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Calidad de Vida / Síndrome de Bardet-Biedl Tipo de estudio: Prognostic_studies Aspecto: Patient_preference Límite: Adolescent / Adult / Child / Humans Idioma: En Revista: Orphanet J Rare Dis Asunto de la revista: MEDICINA Año: 2023 Tipo del documento: Article País de afiliación: Reino Unido
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