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Efficacy of Burosumab in Adults with X-linked Hypophosphatemia (XLH): A Post Hoc Subgroup Analysis of a Randomized Double-Blind Placebo-Controlled Phase 3 Study.
Brandi, Maria Luisa; Jan de Beur, Suzanne; Briot, Karine; Carpenter, Thomas; Cheong, Hae Il; Cohen-Solal, Martine; Crowley, Rachel K; Eastell, Richard; Imanishi, Yasuo; Imel, Erik A; Ing, Steven W; Insogna, Karl; Ito, Nobuaki; Javaid, Kassim; Kamenicky, Peter; Keen, Richard; Kubota, Takuo; Lachmann, Robin H; Perwad, Farzana; Pitukcheewanont, Pisit; Portale, Anthony; Ralston, Stuart H; Tanaka, Hiroyuki; Weber, Thomas J; Yoo, Han-Wook; Sun, Wei; Williams, Angela; Nixon, Annabel; Takeuchi, Yasuhiro.
Afiliação
  • Brandi ML; FIRMO Foundation, Via San Gallo 123, 50100, Florence, Italy. marialuisa@marialuisabrandi.it.
  • Jan de Beur S; Division of Endocrinology and Metabolism, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Briot K; Department of Rheumatology, Cochin Hospital, Paris University, Paris, France.
  • Carpenter T; Department of Pediatrics and Department of Orthopedics and Rehabilitation, Yale School of Medicine, New Haven, CT, USA.
  • Cheong HI; Department of Pediatrics, Seoul National University Children's Hospital, Seoul, Republic of Korea.
  • Cohen-Solal M; Department of Rheumatology, Lariboisière Hospital, INSERM U1132 BIOSCAR, and University of Paris, Paris, France.
  • Crowley RK; Department of Endocrinology, St Vincent's University Hospital, and University College Dublin School of Medicine and Medical Science, Dublin, Ireland.
  • Eastell R; Department of Oncology and Metabolism, University of Sheffield, Sheffield, UK.
  • Imanishi Y; Department of Metabolism, Endocrinology and Molecular Medicine, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan.
  • Imel EA; Department of Medicine and Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, USA.
  • Ing SW; Division of Endocrinology, Diabetes, and Metabolism, Ohio State University Wexner Medical Center, Columbus, OH, USA.
  • Insogna K; Department of Internal Medicine, Yale School of Medicine, New Haven, CT, USA.
  • Ito N; Division of Nephrology and Endocrinology, The University of Tokyo Hospital, Tokyo, Japan.
  • Javaid K; Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, National Institute for Health Research Oxford Biomedical Research Centre, University of Oxford, Oxford, UK.
  • Kamenicky P; Endocrine Physiology and Pathophysiology, INSERM, Paris-Saclay University, and Bicêtre Hospital, Paris, France.
  • Keen R; Metabolic Bone Disease Unit, Royal National Orthopaedic Hospital NHS Trust, London, UK.
  • Kubota T; Department of Pediatrics, Osaka University Graduate School of Medicine, Osaka, Japan.
  • Lachmann RH; Charles Dent Metabolic Unit, National Hospital for Neurology and Neurosurgery, University College London Hospitals NHS Foundation Trust, London, UK.
  • Perwad F; Division of Nephrology, Department of Pediatrics, University of California San Francisco, San Francisco, USA.
  • Pitukcheewanont P; Department of Pediatric Endocrinology, Children's Hospital Los Angeles, University of Southern California Keck School of Medicine, Los Angeles, USA.
  • Portale A; Division of Nephrology, Department of Pediatrics, University of California San Francisco, San Francisco, USA.
  • Ralston SH; Rheumatology and Bone Diseases Unit, Medical Research Council Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, UK.
  • Tanaka H; Department of Pediatrics, Okayama Saiseikai General Hospital, Okayama, Japan.
  • Weber TJ; Division of Endocrinology, Metabolism and Nutrition, Department of Medicine, Duke University Medical Center, Durham, NC, USA.
  • Yoo HW; Department of Pediatrics, Asan Medical Center Children's Hospital, Seoul, Republic of Korea.
  • Sun W; Biostatistics Department, Kyowa Kirin Pharmaceutical Development, Inc., Princeton, NJ, USA.
  • Williams A; Kyowa Kirin International, Marlow, UK.
  • Nixon A; Chilli Consultancy, Salisbury, UK.
  • Takeuchi Y; Endocrine Center, Toranomon Hospital, Tokyo, Japan.
Calcif Tissue Int ; 111(4): 409-418, 2022 10.
Article em En | MEDLINE | ID: mdl-35927518
The anti-fibroblast growth factor 23 monoclonal antibody burosumab corrects hypophosphatemia in adults with X-linked hypophosphatemia (XLH) and improves pain, stiffness, physical function, and fatigue. This post hoc subgroup analysis used data from the 24-week placebo-controlled period of a phase 3 study in 134 adults with XLH (ClinicalTrials.gov NCT02526160), to assess whether the benefits of burosumab are evident in 14 clinically relevant subgroups defined by baseline demographic and functional criteria, including sex, Brief Pain Inventory-short form (BPI-SF) Average And Worst Pain, region, race, Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC®) Stiffness, Physical Function and Pain domains and total score, use of opioid/other pain medication, active fractures/pseudo-fractures, and 6-min walk test distance. There were no statistically significant interactions between any of the subgroups and treatment arm for any endpoint. Higher proportions of subjects achieved mean serum phosphate concentration above the lower limit of normal (the primary endpoint) with burosumab than with placebo in all subgroups. For the key secondary endpoints (WOMAC Stiffness and Physical Function; BPI-SF Worst Pain) individual subgroup categories showed improvements with burosumab relative to placebo. For additional efficacy endpoints, burosumab was favored in some subgroups but differences were not significant and confidence intervals were wide. For some endpoints the treatment effect is small at 24 weeks in all subjects. This subgroup analysis shows that burosumab was largely superior to placebo across endpoints in the 14 clinically relevant subgroup variables at 24 weeks and is likely to benefit all symptomatic adults with active XLH.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Raquitismo Hipofosfatêmico Familiar Idioma: En Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Raquitismo Hipofosfatêmico Familiar Idioma: En Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Itália