About this trial
X-linked hypophosphataemia (XLH) is a rare, hereditary condition. The genetic defect leads to low blood phosphate levels and vitamin D suppression. Phosphate is required for strong bones and teeth and to store energy in cells. Low phosphate leads to soft bones (rickets). Patients experience bowed legs, short stature, bone pain and dental pain.
Prior to Burosumab, conventional treatment of XLH previously consisted of two medications. On this regimen, patients take oral phosphate supplements 4-6 times a day and an active form of vitamin D daily. This treatment can leave patients with residual symptoms. They report significant disabilities and reduced quality of life.
Burosumab (Crysvita, Kyowa Kirin) is now the standard paediatric treatment for XLH. It is given once a fortnight by injection under the skin. Early studies used a starting dose of 0.4mg/kg per dose. NICE recommends a starting dose of 0.4mg/kg, a normal maintenance dose of 0.8mg/kg and a maximum of 2mg/kg (up to 90mg). The British National Formulary for Children (BNFC) gives the same advice.
However, the European Medicines Agency recommends a starting dose of 0.8mg/kg per dose which is, therefore, the standard starting dose now. Some patients achieve symptom and biochemical control on less than 0.8 mg/kg per dose. They may be exposed to higher doses than necessary.
To date, approximately 200 patients have started on Burosumab in England. They are all managed by specialist centres. The rare status of XLH means there are relatively few patients in each centre. Treatment effects and trends can only be described by collating data from multiple centres.
The investigators will undertake a review across multiple English centres of the doses of Burosumab. The review will only collect data already in the patients' health records. It will look at factors affecting the starting dose. The investigators will assess the association between dose, blood markers and growth.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
A diagnosis of x-linked hypophosphataemia (XLH) including genetic confirmation of a PHEX mutation.
Has received at least 12 months of continuous Burosumab treatment under paediatric criteria (given Burosumab is not started till a child is 12 months old in England, the minimum age will, therefore, be 2 years old) prior to their 18th birthday.
Disqualifiers
Burosumab received under adult criteria (patients who have received both Burosumab under paediatric arrangements and, subsequently, adult arrangements, can have data obtained during paediatric dosing included).
Trial population
Patients with XLH treated with Burosumab under the care of participating centres.
Trial design
Cohort
Retrospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
The proportion of patients who achieved biochemical control (serum phosphate above the lower limit of the local reference range) on a dose of less than 0.8 mg/kg per dose of Burosumab.
Secondary outcomes
Comparison of outcomes for patients started on Burosumab at a dose of less than 0.8 mg/kg per dose with those started on a dose of 0.8 mg/kg per dose and above - time to biochemical control
• Mean difference in time to achieve biochemical control (serum phosphate above the lower limit of the local reference range).
Comparison of outcomes for patients started on Burosumab at a dose of less than 0.8 mg/kg per dose with those started on a dose of 0.8 mg/kg per dose and above - change in height SDS
• Mean difference in change in height SDS after 12 months of treatment.
Comparison of outcomes for patients started on Burosumab at a dose of less than 0.8 mg/kg per dose with those started on a dose of 0.8 mg/kg per dose and above - dose difference
• Mean difference in dose of Burosumab at 12 months after first dose.
Comparison of outcomes for patients started on Burosumab at a dose of less than 0.8 mg/kg per dose with those started on a dose of 0.8 mg/kg per dose and above - cost difference
• Mean difference in cost of giving Burosumab.
Sponsors and contacts
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University of Nottingham
Lead sponsor
Nottingham University Hospitals NHS Trust
Collaborator
Birmingham Women's and Children's NHS Foundation Trust
Collaborator
University Hospitals Bristol and Weston NHS Foundation Trust
Collaborator
University Hospital Southampton NHS Foundation Trust
Collaborator
Sheffield Children's NHS Foundation Trust
Collaborator
Manchester University NHS Foundation Trust
Collaborator
Newcastle-upon-Tyne Hospitals NHS Trust
Collaborator
Alder Hey Children's NHS Foundation Trust
Collaborator