TY - JOUR
T1 - Burosumab vs conventional therapy in children with X-linked hypophosphatemia
T2 - Results of the open-label, phase 3 extension period
AU - Ward, Leanne M.
AU - Högler, Wolfgang
AU - Glorieux, Francis H.
AU - Portale, Anthony A.
AU - Whyte, Michael P.
AU - Munns, Craig F.
AU - Nilsson, Ola
AU - Simmons, Jill H.
AU - Padidela, Raja
AU - Namba, Noriyuki
AU - Cheong, Hae Il
AU - Sochett, Etienne
AU - Muroya, Koji
AU - Tanaka, Hiroyuki
AU - Pitukcheewanont, Pisit
AU - Gottesman, Gary S.
AU - Biggin, Andrew
AU - Perwad, Farzana
AU - Chen, Angel
AU - Lawrence Merritt, John
AU - Imel, Erik A.
N1 - Publisher Copyright:
© 2024 The Author(s). Published by Oxford University Press on behalf of the American Society for Bone and Mineral Research.
PY - 2024/1
Y1 - 2024/1
N2 - 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.
AB - 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.
KW - FGF23
KW - burosumab
KW - phosphate
KW - rare disease
KW - x-linked hypophosphatemia
UR - http://www.scopus.com/inward/record.url?scp=85193424229&partnerID=8YFLogxK
U2 - 10.1093/jbmrpl/ziad001
DO - 10.1093/jbmrpl/ziad001
M3 - Article
C2 - 38690124
AN - SCOPUS:85193424229
SN - 2473-4039
VL - 8
JO - JBMR Plus
JF - JBMR Plus
IS - 1
M1 - ziad001
ER -