Burosumab vs conventional therapy in children with X-linked hypophosphatemia: results of the open-label, phase 3 extension period

Author:

Ward Leanne M12,Högler Wolfgang34,Glorieux Francis H5,Portale Anthony A6,Whyte Michael P7,Munns Craig F8910,Nilsson Ola11121314,Simmons Jill H1516,Padidela Raja17,Namba Noriyuki1819,Cheong Hae Il20,Sochett Etienne21,Muroya Koji22,Tanaka Hiroyuki23,Pitukcheewanont Pisit24,Gottesman Gary S7,Biggin Andrew25,Perwad Farzana6,Chen Angel26,Lawrence Merritt II John26,Imel Erik A27

Affiliation:

1. Department of Pediatrics , Faculty of Medicine, , Ottawa, Ontario, K1H 8L1 , Canada

2. University of Ottawa , Faculty of Medicine, , Ottawa, Ontario, K1H 8L1 , Canada

3. Department of Paediatrics and Adolescent Medicine, Johannes Kepler University Linz , 4040 Linz , Austria

4. Institute of Metabolism and Systems Research, University of Birmingham , Edgbaston, Birmingham, B15 2TT , United Kingdom

5. Department of Surgery, Pediatrics, and Human Genetics, Shriners Hospitals for Children and McGill University , Montreal, Quebec, H4A 0A9 , Canada

6. Department of Pediatrics, University of California , San Francisco, CA, 94158 , United States

7. Shriners Hospitals for Children St Louis , St Louis, MO, 63110 , United States

8. Faculty of Medicine, The University of Queensland , Brisbane, Queensland, 4072 , Australia

9. Faculty of Medicine, Child Health Research Centre, The University of Queensland , Brisbane, Queensland, 4072 , Australia

10. Department of Endocrinology and Diabetes, Queensland Children’s Hospital , Brisbane, Queensland, 4072 , Australia

11. Division of Pediatric Endocrinology , Department of Women’s and Children’s Health, , SE-17176 Stockholm , Sweden

12. Center for Molecular Medicine, Karolinska Institutet and University Hospital , Department of Women’s and Children’s Health, , SE-17176 Stockholm , Sweden

13. Department of Pediatrics , School of Medical Sciences, , S-701 82 Örebro , Sweden

14. Örebro University and University Hospital , School of Medical Sciences, , S-701 82 Örebro , Sweden

15. Division of Endocrinology and Diabetes , Department of Pediatrics, , Nashville, TN, 37232 , United States

16. Vanderbilt University School of Medicine, Vanderbilt University , Department of Pediatrics, , Nashville, TN, 37232 , United States

17. Department of Paediatric Endocrinology, Royal Manchester Children’s Hospital , Manchester, M13 9WL , United Kingdom

18. Department of Pediatrics, Osaka Hospital, Japan Community Healthcare Organization , Osaka, 553-0003 , Japan

19. Osaka University Graduate School of Medicine , Osaka, 565-0871 , Japan

20. Department of Pediatrics, Hallym University Sacred Heart Hospital , Dongan-gu, Anyang, 14068 , South Korea

21. Department of Pediatrics, Hospital for Sick Children , Toronto, Ontario, M5G 1E8 , Canada

22. Department of Endocrinology, Kanagawa Children’s Medical Center , Yokohama, Kanagawa 232-0066 , Japan

23. Division of Pediatrics, Okayama Saiseikai General Hospital Outpatient Center , Kita-ku, Okayama, 700-8511 , Japan

24. Center of Endocrinology, Diabetes and Metabolism, Children’s Hospital of Los Angeles , Los Angeles, CA, 90027 , United States

25. Department of Endocrinology, The University of Sydney Children’s Hospital Westmead Clinical School, The Children’s Hospital at Westmead , Westmead, New South Wales, 2145 , Australia

26. Ultragenyx Pharmaceutical Inc. , Novato, CA, 94949 , United States

27. Department of Medicine, Indiana University School of Medicine , Indianapolis, IN, 46202 , United States

Abstract

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.

Funder

Ultragenyx Pharmaceutical Inc

Indiana Clinical and Translational Sciences Institute

National Institutes of Health

National Center for Advancing Translational Sciences, Clinical, and Translational Sciences Award

Publisher

Oxford University Press (OUP)

Subject

Orthopedics and Sports Medicine,Endocrinology, Diabetes and Metabolism

Reference25 articles.

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4. New perspectives on the biology and treatment of X-linked hypophosphatemic rickets;Carpenter;Pediatr Clin N Am,1997

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