Randomised trial of block and replace vs dose titration thionamide in young people with thyrotoxicosis.


Journal

European journal of endocrinology
ISSN: 1479-683X
Titre abrégé: Eur J Endocrinol
Pays: England
ID NLM: 9423848

Informations de publication

Date de publication:
Dec 2020
Historique:
received: 03 06 2020
accepted: 18 09 2020
entrez: 27 10 2020
pubmed: 28 10 2020
medline: 11 11 2020
Statut: ppublish

Résumé

First-line treatment of thyrotoxicosis in young people is thionamide anti-thyroid drug (ATD) in a blocking dose with levothyroxine replacement (block and replace, BR) or in a smaller dose tailored to render the patient euthyroid (dose titration, DT). Our objective was to determine which regimen provides more stable biochemical control. A multi-centre phase III, open-label randomised trial comparing BR with DT in patients aged 2-17 years with newly diagnosed thyrotoxicosis at 15 UK centres. Patients were randomised shortly after diagnosis and treated for 3 years. The primary outcome was the percentage of serum thyroid-stimulating hormone (TSH) levels in the reference range between 6 months and 3 years. Secondary outcomes included the proportion of Free thyroxine (FT4) levels in the reference range, adverse event frequency and 4 years outcome (remission/relapse). Eighty-two patients were randomised, with details on clinical course in 81 (62 Female); 40 were allocated to BR (41 DT). Three withdrew with one ineligible. The mean percentage of serum TSH within reference range was 60.2% in BR and 63.8% in DT patients; adjusted difference 4.3%, 95% CI (-7.8 to 16.4); P = 0.48. Proportions for FT4 were 79.2% in BR and 85.7% in DT patients; adjusted difference 6.8%, (-0.2 to 15.6); P = 0.13. Three patients developed neutropenia - all on BR. 6 BR and 10 DT patients were in remission at 4y. This randomised trial has shown no evidence to suggest that BR, when managing the young patient with thyrotoxicosis, is associated with improved biochemical stability when compared to DT.

Identifiants

pubmed: 33107439
doi: 10.1530/EJE-20-0617
pii: EJE-20-0617
doi:
pii:

Substances chimiques

Antithyroid Agents 0
Thyrotropin 9002-71-5
Thyroxine Q51BO43MG4

Types de publication

Clinical Trial, Phase III Journal Article Multicenter Study Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

637-645

Subventions

Organisme : Medical Research Council
ID : G0500783
Pays : United Kingdom

Auteurs

Claire L Wood (CL)

Department of Paediatric Endocrinology, Royal Victoria Infirmary, Newcastle-upon-Tyne, UK.
Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, International Centre for Life, Central Parkway, Newcastle upon Tyne, UK.

Michael Cole (M)

Population Health Sciences Institute, Newcastle University, Baddiley-Clark Building, Newcastle upon Tyne, UK.

Malcolm Donaldson (M)

Department of Child Health, University of Glasgow School of Medicine, Glasgow, UK.

David B Dunger (DB)

Department of Paediatrics, University of Cambridge, Cambridge Biomedical Campus, Cambridge, UK.
Wellcome Trust-MRC Institute of Metabolic Sciences, University of Cambridge, Cambridge, UK.

Ruth Wood (R)

Newcastle Clinical Trials Unit, Statistics & Physics, Newcastle University, Newcastle-upon-Tyne, UK.

Niamh Morrison (N)

Department of Paediatric Endocrinology, Royal Victoria Infirmary, Newcastle-upon-Tyne, UK.

John N S Matthews (JNS)

School of Mathematics, Statistics & Physics, Newcastle University, Newcastle-upon-Tyne, UK.
School of Mathematics, Statistics & Physics, Newcastle University, Newcastle-upon-Tyne, UK.

Simon H S Pearce (SHS)

Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, International Centre for Life, Central Parkway, Newcastle upon Tyne, UK.
Department of Endocrinology, Royal Victoria Infirmary, Newcastle-upon-Tyne, UK.

Timothy D Cheetham (TD)

Department of Paediatric Endocrinology, Royal Victoria Infirmary, Newcastle-upon-Tyne, UK.
Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, International Centre for Life, Central Parkway, Newcastle upon Tyne, UK.

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Classifications MeSH