Patient-Reported Outcomes from a Randomized, Active-Controlled, Open-Label, Phase 3 Trial of Burosumab Versus Conventional Therapy in Children with X-Linked Hypophosphatemia.

Burosumab Patient-reported outcomes Patient-reported outcomes measurement information system X-linked hypophosphatemia

Journal

Calcified tissue international
ISSN: 1432-0827
Titre abrégé: Calcif Tissue Int
Pays: United States
ID NLM: 7905481

Informations de publication

Date de publication:
05 2021
Historique:
received: 01 10 2020
accepted: 14 12 2020
pubmed: 24 1 2021
medline: 19 8 2021
entrez: 23 1 2021
Statut: ppublish

Résumé

Changing to burosumab, a monoclonal antibody targeting fibroblast growth factor 23, significantly improved phosphorus homeostasis, rickets, lower-extremity deformities, mobility, and growth versus continuing oral phosphate and active vitamin D (conventional therapy) in a randomized, open-label, phase 3 trial involving children aged 1-12 years with X-linked hypophosphatemia. Patients were randomized (1:1) to subcutaneous burosumab or to continue conventional therapy. We present patient-reported outcomes (PROs) from this trial for children aged ≥ 5 years at screening (n = 35), using a Patient-Reported Outcomes Measurement Information System (PROMIS) questionnaire and SF-10 Health Survey for Children. PROMIS pain interference, physical function mobility, and fatigue scores improved from baseline with burosumab at weeks 40 and 64, but changed little with continued conventional therapy. Pain interference scores differed significantly between groups at week 40 (- 5.02, 95% CI - 9.29 to - 0.75; p = 0.0212) but not at week 64. Between-group differences were not significant at either week for physical function mobility or fatigue. Reductions in PROMIS pain interference and fatigue scores from baseline were clinically meaningful with burosumab at weeks 40 and 64 but not with conventional therapy. SF-10 physical health scores (PHS-10) improved significantly with burosumab at week 40 (least-squares mean [standard error] + 5.98 [1.79]; p = 0.0008) and week 64 (+ 5.93 [1.88]; p = 0.0016) but not with conventional therapy (between-treatment differences were nonsignificant). In conclusion, changing to burosumab improved PRO measures, with statistically significant differences in PROMIS pain interference at week 40 versus continuing with conventional therapy and in PHS-10 at weeks 40 and 64 versus baseline.Trial registration: ClinicalTrials.gov NCT02915705.

Identifiants

pubmed: 33484279
doi: 10.1007/s00223-020-00797-x
pii: 10.1007/s00223-020-00797-x
pmc: PMC8064984
doi:

Substances chimiques

Antibodies, Monoclonal 0
Antibodies, Monoclonal, Humanized 0
burosumab G9WJT6RD29

Banques de données

ClinicalTrials.gov
['NCT02915705']

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

622-633

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Auteurs

Raja Padidela (R)

Department of Paediatric Endocrinology, Royal Manchester Children's Hospital, Manchester, UK. Raja.Padidela@mft.nhs.uk.
Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK. Raja.Padidela@mft.nhs.uk.

Michael P Whyte (MP)

Shriners Hospitals for Children -Washington University School of Medicine in St Louis, St Louis, MO, USA.

Francis H Glorieux (FH)

Shriners Hospital for Children - Canada, McGill University, Montreal, QC, Canada.

Craig F Munns (CF)

The University of Sydney Children's Hospital Westmead Clinical School, The Children's Hospital at Westmead, Westmead, NSW, Australia.
Department of Endocrinology, The Children's Hospital at Westmead, Westmead, NSW, Australia.

Leanne M Ward (LM)

Department of Pediatrics, University of Ottawa, Ottawa, ON, Canada.
Division of Endocrinology and Metabolism, Children's Hospital of Eastern Ontario, Ottawa, ON, Canada.

Ola Nilsson (O)

Division of Pediatric Endocrinology & Center for Molecular Medicine, Karolinska Institute, Stockholm, Sweden.
School of Medical Sciences, Örebro University, Örebro, Sweden.

Anthony A Portale (AA)

Department of Pediatrics, University of California, San Francisco, San Francisco, CA, USA.

Jill H Simmons (JH)

Departments of Pediatrics, Division of Endocrinology and Diabetes, Vanderbilt University School of Medicine, Vanderbilt University, Nashville, TN, USA.

Noriyuki Namba (N)

Department of Pediatrics, Osaka Hospital, Japan Community Healthcare Organization, Osaka, Japan.
Department of Pediatrics, Osaka University Graduate School of Medicine, Osaka, Japan.

Hae Il Cheong (HI)

Seoul National University Children's Hospital, Seoul, Republic of Korea.

Pisit Pitukcheewanont (P)

Center of Endocrinology, Diabetes and Metabolism, Children's Hospital Los Angeles, Los Angeles, CA, USA.

Etienne Sochett (E)

Department of Paediatrics, Hospital for Sick Children, Toronto, ON, Canada.

Wolfgang Högler (W)

Department of Paediatrics and Adolescent Medicine, Johannes Kepler University Linz, Linz, Austria.
Institute of Metabolism and Systems Research, University of Birmingham, Birmingham, UK.

Koji Muroya (K)

Department of Endocrinology and Metabolism, Kanagawa Children's Medical Center, Yokohama, Japan.

Hiroyuki Tanaka (H)

Okayama Saiseikai General Hospital Outpatient Center, Okayama, Japan.

Gary S Gottesman (GS)

Shriners Hospitals for Children, St Louis, MO, USA.

Andrew Biggin (A)

The University of Sydney Children's Hospital Westmead Clinical School, The Children's Hospital at Westmead, Westmead, NSW, Australia.

Farzana Perwad (F)

Department of Pediatrics, University of California, San Francisco, San Francisco, CA, USA.

Angela Williams (A)

Kyowa Kirin International, Marlow, UK.

Annabel Nixon (A)

Chilli Consultancy, Salisbury, UK.

Wei Sun (W)

Kyowa Kirin Pharmaceutical Development, Princeton, NJ, USA.

Angel Chen (A)

Ultragenyx Pharmaceutical, Novato, CA, USA.

Alison Skrinar (A)

Ultragenyx Pharmaceutical, Novato, CA, USA.

Erik A Imel (EA)

Department of Medicine and Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, USA.

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