Literature DB >> 33984553

Burosumab treatment for fibrous dysplasia.

Anne Gladding1, Vivian Szymczuk2, Bethany A Auble1, Alison M Boyce3.   

Abstract

BACKGROUND: Fibrous dysplasia/McCune-Albright syndrome (FD/MAS) is a rare mosaic disorder of Gαs activation. Fibroblast Growth Factor 23 (FGF23)-mediated hypophosphatemia is a feature of FD/MAS that has been associated with poor skeletal outcomes. Standard therapy includes oral phosphorus and vitamin D analogs; however, treatment is limited by potential adverse renal and gastrointestinal effects. Burosumab is a monoclonal antibody to FGF23 approved to treat patients with X-linked hypophosphatemia and tumor-induced osteomalacia. There is currently no safety or efficacy data to support burosumab use in patients with FD/MAS. CASE DESCRIPTION: A 7-year-old boy with severe FD/MAS presented with persistent hypophosphatemia and skeletal complications despite conventional treatment with oral phosphate and calcitriol. He was started on burosumab and achieved sustained normalization of serum phosphorus and marked improvement in alkaline phosphatase levels. This was accompanied by an encouraging clinical response, including decreased bone pain, improved muscle strength, and improved ambulation. No adverse effects of burosumab therapy were observed.
CONCLUSIONS: This is the first reported case of burosumab treatment in a patient with FD/MAS. The encouraging biochemical and clinical response in this patient highlights the need for future studies to explore the safety and efficacy of burosumab in the FD/MAS pediatric population. Published by Elsevier Inc.

Entities:  

Keywords:  FGF23; Hypophosphatemia; McCune-Albright syndrome; Osteomalacia; Rickets

Mesh:

Substances:

Year:  2021        PMID: 33984553      PMCID: PMC8272883          DOI: 10.1016/j.bone.2021.116004

Source DB:  PubMed          Journal:  Bone        ISSN: 1873-2763            Impact factor:   4.626


  22 in total

1.  Disease severity and functional factors associated with walking performance in polyostotic fibrous dysplasia.

Authors:  Scott M Paul; Lisa R Gabor; Scott Rudzinski; David Giovanni; Alison M Boyce; Marilyn R N Kelly; Michael T Collins
Journal:  Bone       Date:  2013-12-04       Impact factor: 4.398

2.  Patients with McCune-Albright syndrome have a broad spectrum of abnormalities in the gastrointestinal tract and pancreas.

Authors:  Laura D Wood; Michaël Noë; Wenzel Hackeng; Lodewijk A A Brosens; Feriyl Bhaijee; Marija Debeljak; Jun Yu; Masaya Suenaga; Aatur D Singhi; Atif Zaheer; Alison Boyce; Cemre Robinson; James R Eshleman; Michael G Goggins; Ralph H Hruban; Michael T Collins; Anne Marie Lennon; Elizabeth A Montgomery
Journal:  Virchows Arch       Date:  2017-02-10       Impact factor: 4.064

Review 3.  Tumor-Induced Osteomalacia.

Authors:  Pablo Florenzano; Iris R Hartley; Macarena Jimenez; Kelly Roszko; Rachel I Gafni; Michael T Collins
Journal:  Calcif Tissue Int       Date:  2020-06-05       Impact factor: 4.333

Review 4.  Fibrous dysplasia and fibroblast growth factor-23 regulation.

Authors:  Alison M Boyce; Nisan Bhattacharyya; Michael T Collins
Journal:  Curr Osteoporos Rep       Date:  2013-06       Impact factor: 5.096

Review 5.  Bisphosphonate nephrotoxicity.

Authors:  Mark A Perazella; Glen S Markowitz
Journal:  Kidney Int       Date:  2008-08-06       Impact factor: 10.612

6.  The histopathology of fibrous dysplasia of bone in patients with activating mutations of the Gs alpha gene: site-specific patterns and recurrent histological hallmarks.

Authors:  M Riminucci; B Liu; A Corsi; A Shenker; A M Spiegel; P G Robey; P Bianco
Journal:  J Pathol       Date:  1999-01       Impact factor: 7.996

Review 7.  McCune-Albright syndrome and the extraskeletal manifestations of fibrous dysplasia.

Authors:  Michael T Collins; Frederick R Singer; Erica Eugster
Journal:  Orphanet J Rare Dis       Date:  2012-05-24       Impact factor: 4.123

Review 8.  Best practice management guidelines for fibrous dysplasia/McCune-Albright syndrome: a consensus statement from the FD/MAS international consortium.

Authors:  Muhammad Kassim Javaid; Alison Boyce; Natasha Appelman-Dijkstra; Juling Ong; Patrizia Defabianis; Amaka Offiah; Paul Arundel; Nick Shaw; Valter Dal Pos; Ann Underhil; Deanna Portero; Lisa Heral; Anne-Marie Heegaard; Laura Masi; Fergal Monsell; Robert Stanton; Pieter Durk Sander Dijkstra; Maria Luisa Brandi; Roland Chapurlat; Neveen Agnes Therese Hamdy; Michael Terrence Collins
Journal:  Orphanet J Rare Dis       Date:  2019-06-13       Impact factor: 4.123

9.  FGF-23 in fibrous dysplasia of bone and its relationship to renal phosphate wasting.

Authors:  Mara Riminucci; Michael T Collins; Neal S Fedarko; Natasha Cherman; Alessandro Corsi; Kenneth E White; Steven Waguespack; Anurag Gupta; Tamara Hannon; Michael J Econs; Paolo Bianco; Pamela Gehron Robey
Journal:  J Clin Invest       Date:  2003-09       Impact factor: 14.808

Review 10.  Fibrous Dysplasia/McCune-Albright Syndrome: A Rare, Mosaic Disease of Gα s Activation.

Authors:  Alison M Boyce; Michael T Collins
Journal:  Endocr Rev       Date:  2020-04-01       Impact factor: 19.871

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  3 in total

1.  Burosumab Treatment for Autosomal Recessive Hypophosphatemic Rickets Type 1 (ARHR1).

Authors:  Xiuying Bai; Mark Levental; Andrew C Karaplis
Journal:  J Clin Endocrinol Metab       Date:  2022-09-28       Impact factor: 6.134

2.  A case report to assess the safety and efficacy of Burosumab, an investigational antibody to FGF23, in a single pediatric patient with Epidermal Nevus Syndrome and associated hypophosphatemic rickets.

Authors:  Carson Huynh; Andrea Gillis; Jessica Fazendin; Hussein Abdullatif
Journal:  Bone Rep       Date:  2022-07-20

3.  Rickets guidance: part II-management.

Authors:  Dieter Haffner; Maren Leifheit-Nestler; Andrea Grund; Dirk Schnabel
Journal:  Pediatr Nephrol       Date:  2022-03-29       Impact factor: 3.651

  3 in total

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