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Burosumab vs conventional therapy in children with X-linked hypophosphatemia: results of the open-label, phase 3 extension period.
Ward, Leanne M; Högler, Wolfgang; Glorieux, Francis H; Portale, Anthony A; Whyte, Michael P; Munns, Craig F; Nilsson, Ola; Simmons, Jill H; Padidela, Raja; Namba, Noriyuki; Cheong, Hae Il; Sochett, Etienne; Muroya, Koji; Tanaka, Hiroyuki; Pitukcheewanont, Pisit; Gottesman, Gary S; Biggin, Andrew; Perwad, Farzana; Chen, Angel; Lawrence Merritt Ii, John; Imel, Erik A.
Afiliação
  • Ward LM; Department of Pediatrics, Faculty of Medicine, University of Ottawa, Ottawa, Ontario, K1H 8L1, Canada.
  • Högler W; Department of Paediatrics and Adolescent Medicine, Johannes Kepler University Linz, 4040 Linz, Austria.
  • Glorieux FH; Institute of Metabolism and Systems Research, University of Birmingham, Edgbaston, Birmingham, B15 2TT, United Kingdom.
  • Portale AA; Department of Surgery, Pediatrics, and Human Genetics, Shriners Hospitals for Children and McGill University, Montreal, Quebec, H4A 0A9, Canada.
  • Whyte MP; Department of Pediatrics, University of California, San Francisco, CA, 94158, United States.
  • Munns CF; Shriners Hospitals for Children St Louis, St Louis, MO, 63110, United States.
  • Nilsson O; Faculty of Medicine, The University of Queensland, Brisbane, Queensland, 4072, Australia.
  • Simmons JH; Faculty of Medicine, Child Health Research Centre, The University of Queensland, Brisbane, Queensland, 4072, Australia.
  • Padidela R; Department of Endocrinology and Diabetes, Queensland Children's Hospital, Brisbane, Queensland, 4072, Australia.
  • Namba N; Division of Pediatric Endocrinology, Department of Women's and Children's Health, Center for Molecular Medicine, Karolinska Institutet and University Hospital, SE-17176 Stockholm, Sweden.
  • Cheong HI; Department of Pediatrics, School of Medical Sciences, Örebro University and University Hospital, S-701 82 Örebro, Sweden.
  • Sochett E; Division of Endocrinology and Diabetes, Department of Pediatrics, Vanderbilt University School of Medicine, Vanderbilt University, Nashville, TN, 37232, United States.
  • Muroya K; Department of Paediatric Endocrinology, Royal Manchester Children's Hospital, Manchester, M13 9WL, United Kingdom.
  • Tanaka H; Department of Pediatrics, Osaka Hospital, Japan Community Healthcare Organization, Osaka, 553-0003, Japan.
  • Pitukcheewanont P; Osaka University Graduate School of Medicine, Osaka, 565-0871, Japan.
  • Gottesman GS; Department of Pediatrics, Hallym University Sacred Heart Hospital, Dongan-gu, Anyang, 14068, South Korea.
  • Biggin A; Department of Pediatrics, Hospital for Sick Children, Toronto, Ontario, M5G 1E8, Canada.
  • Perwad F; Department of Endocrinology, Kanagawa Children's Medical Center, Yokohama, Kanagawa 232-0066, Japan.
  • Chen A; Division of Pediatrics, Okayama Saiseikai General Hospital Outpatient Center, Kita-ku, Okayama, 700-8511, Japan.
  • Lawrence Merritt Ii J; Center of Endocrinology, Diabetes and Metabolism, Children's Hospital of Los Angeles, Los Angeles, CA, 90027, United States.
  • Imel EA; Shriners Hospitals for Children St Louis, St Louis, MO, 63110, United States.
JBMR Plus ; 8(1): ziad001, 2024 Jan.
Article em En | MEDLINE | ID: mdl-38690124
ABSTRACT
In a randomized, open-label phase 3 study of 61 children aged 1-12 years old with X-linked hypophosphatemia (XLH) previously treated with conventional therapy, changing to burosumab every 2 weeks (Q2W) for 64 weeks improved the phosphate metabolism, radiographic rickets, and growth compared with conventional therapy. In this open-label extension period (weeks 64-88), 21 children continued burosumab Q2W at the previous dose or crossed over from conventional therapy to burosumab starting at 0.8 mg/kg Q2W with continued clinical radiographic assessments through week 88. Efficacy endpoints and safety observations were summarized descriptively for both groups (burosumab continuation, n = 6; crossover, n = 15). At week 88 compared with baseline, improvements in the following outcomes were observed in the burosumab continuation and crossover groups, respectively mean (SD) RGI-C rickets total score (primary outcome), +2.11 (0.27) and +1.89 (0.35); mean (SD) RGI-C lower limb deformity score, +1.61 (0.91) and +0.73 (0.82); and mean (SD) height Z-score + 0.41 (0.50) and +0.08 (0.34). Phosphate metabolism normalized rapidly in the crossover group and persisted in the continuation group. Mean (SD) serum alkaline phosphatase decreased from 169% (43%) of the upper limit of normal (ULN) at baseline to 126% (51%) at week 88 in the continuation group and from 157% (33%) of the ULN at baseline to 111% (23%) at week 88 in the crossover group. During the extension period, treatment-emergent adverse events (AEs) were reported in all 6 children in the burosumab continuation group and 14/15 children in the crossover group. The AE profiles in the randomized and extension periods were similar, with no new safety signals identified. Improvements from baseline in radiographic rickets continued in the extension period among children with XLH who remained on burosumab. Children who crossed over from conventional therapy to burosumab demonstrated a rapid improvement in phosphate metabolism and improved rickets healing over the ensuing 22 weeks.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article