TY - JOUR
T1 - Effect of Burosumab Compared With Conventional Therapy on Younger vs Older Children With X-linked Hypophosphatemia
AU - Ward, Leanne M.
AU - Glorieux, Francis H.
AU - Whyte, Michael P.
AU - Munns, Craig F.
AU - Portale, Anthony A.
AU - Hogler, Wolfgang
AU - Simmons, Jill H.
AU - Gottesman, Gary S.
AU - Padidela, Raja
AU - Namba, Noriyuki
AU - Cheong, Hae Il
AU - Nilsson, Ola
AU - Mao, Meng
AU - Chen, Angel
AU - Skrinar, Alison
AU - Roberts, Mary Scott
AU - Imel, Erik A.
N1 - Funding Information:
L.M.W. has been a consultant to, and participated in clinical trials with, Ultragenyx Pharmaceutical Inc. (with funds to Dr Ward’s institution). F.H.G. has been a consultant to, and participated in clinical trials with, Ultragenyx Pharmaceutical Inc. M.P.W. has no conflicts to disclose within the last 2 years. C.F.M. is a consultant for Kyowa Kirin and has received research funding from Kyowa Kirin. A.A.P. has been a consultant to, and served as an investigator in clinical trials with, Ultragenyx Pharmaceutical Inc. W.H. served as an investigator in clinical trials with, and as a consultant for, Ultragenyx Pharmaceutical Inc. and serves as a clinical investigator in clinical trials with, and has received research funding from, Kyowa Kirin. J.H.S. has received institutional research funding from and personal honoraria for participation in an advisory board from Ultragenyx Pharmaceutical Inc. G.S.G. has been a consultant for Ultragenyx Pharmaceutical Inc. R.P. has no conflicts to disclose within the last 2 years. N.N. has been a consultant to, and participated in clinical trials with, Kyowa Kirin. H.I.C. has been a consultant to, and participated in clinical trials with, Ultragenyx Pharmaceutical Inc. O.N. has received speakers’ honoraria from Kyowa Kirin, Abbott, and Biomarin, consulting fees from Kyowa Kirin and Biomarin, and research support from Kyowa Kirin. M.M., A.C., A.S., and M.S.R. report employment by, and stock ownership in, Ultragenyx Pharmaceutical Inc. E.A.I. has been a consultant to, and participated in clinical trials with, Ultragenyx Pharmaceutical Inc.
Publisher Copyright:
© 2022 Endocrine Society. All rights reserved.
PY - 2022/8/1
Y1 - 2022/8/1
N2 - Context: Younger age at treatment onset with conventional therapy (phosphate salts and active vitamin D; Pi/D) is associated with improved growth and skeletal outcomes in children with X-linked hypophosphatemia (XLH). The effect of age on burosumab efficacy and safety in XLH is unknown. Objective: This work aimed to explore the efficacy and safety of burosumab vs Pi/D in younger (< 5 years) and older (5-12 years) children with XLH. Methods: This post hoc analysis of a 64-week, open-label, randomized controlled study took place at 16 academic centers. Sixty-one children aged 1 to 12 years with XLH (younger, n = 26; older, n = 35) participated. Children received burosumab starting at 0.8 mg/kg every 2 weeks (younger, n = 14; older, n = 15) or continued Pi/D individually titrated per recommended guidelines (younger, n = 12; older, n = 20). The main outcome measure included the least squares means difference (LSMD) in Radiographic Global Impression of Change (RGI-C) rickets total score from baseline to week 64. Results: The LSMD in outcomes through 64 weeks on burosumab vs conventional therapy by age group were as follows: RGI-C rickets total score (younger, +0.90; older, +1.07), total Rickets Severity Score (younger, -0.86; older, -1.44), RGI-C lower limb deformity score (younger, +1.02; older, +0.91), recumbent length or standing height Z-score (younger, +0.20; older, +0.09), and serum alkaline phosphatase (ALP) (younger, -31.15% of upper normal limit [ULN]; older, -52.11% of ULN). On burosumab, dental abscesses were not reported in younger children but were in 53% of older children. Conclusion: Burosumab appears to improve outcomes both in younger and older children with XLH, including rickets, lower limb deformities, growth, and ALP, compared with Pi/D.
AB - Context: Younger age at treatment onset with conventional therapy (phosphate salts and active vitamin D; Pi/D) is associated with improved growth and skeletal outcomes in children with X-linked hypophosphatemia (XLH). The effect of age on burosumab efficacy and safety in XLH is unknown. Objective: This work aimed to explore the efficacy and safety of burosumab vs Pi/D in younger (< 5 years) and older (5-12 years) children with XLH. Methods: This post hoc analysis of a 64-week, open-label, randomized controlled study took place at 16 academic centers. Sixty-one children aged 1 to 12 years with XLH (younger, n = 26; older, n = 35) participated. Children received burosumab starting at 0.8 mg/kg every 2 weeks (younger, n = 14; older, n = 15) or continued Pi/D individually titrated per recommended guidelines (younger, n = 12; older, n = 20). The main outcome measure included the least squares means difference (LSMD) in Radiographic Global Impression of Change (RGI-C) rickets total score from baseline to week 64. Results: The LSMD in outcomes through 64 weeks on burosumab vs conventional therapy by age group were as follows: RGI-C rickets total score (younger, +0.90; older, +1.07), total Rickets Severity Score (younger, -0.86; older, -1.44), RGI-C lower limb deformity score (younger, +1.02; older, +0.91), recumbent length or standing height Z-score (younger, +0.20; older, +0.09), and serum alkaline phosphatase (ALP) (younger, -31.15% of upper normal limit [ULN]; older, -52.11% of ULN). On burosumab, dental abscesses were not reported in younger children but were in 53% of older children. Conclusion: Burosumab appears to improve outcomes both in younger and older children with XLH, including rickets, lower limb deformities, growth, and ALP, compared with Pi/D.
KW - X-linked hypophosphatemia
KW - burosumab
KW - children
KW - fibroblast growth factor 23
KW - rickets
UR - http://www.scopus.com/inward/record.url?scp=85134428269&partnerID=8YFLogxK
U2 - 10.1210/clinem/dgac296
DO - 10.1210/clinem/dgac296
M3 - Article
C2 - 35533340
AN - SCOPUS:85134428269
VL - 107
SP - E3241-E3253
JO - Journal of Clinical Endocrinology and Metabolism
JF - Journal of Clinical Endocrinology and Metabolism
SN - 0021-972X
IS - 8
ER -