Evidence map›Paper›PMID 34687316›Full record

Trial reportThe Journal of clinical endocrinology and metabolism2022

Adjuvant Rituximab-Exploratory Trial in Young People With Graves Disease.

Tim D Cheetham, Michael Cole, Mario Abinun, Amit Allahabadia, Tim Barratt, Justin H Davies, Paul Dimitri, Amanda Drake, Zainaba Mohamed, Robert D Murray and 8 more

Open access · hybridAbstract readClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in The Journal of clinical endocrinology and metabolism, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.0field-weighted citation impact, top 21% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Review
  3. Observational
  4. Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Characterizing the Interplay of Lymphocytes in Graves' Disease.International journal of molecular sciences · 2023
    Review
  12. Graves' disease: moving forwards.Archives of disease in childhood · 2023
    Review
  13. Graves' Disease in Children: An Update.Clinical medicine insights. Endocrinology and diabetes · 2023
    Review
  14. Review
  15. Graves' Disease in the Young: Could We Change the Weather?The Journal of clinical endocrinology and metabolism · 2022
    Article
  16. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors.

Tim D CheethamTranslational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, International Centre for Life, Newcastle upon Tyne, NE1 3BZ, UK.ORCID 0000-0003-3120-2513
Michael ColePopulation Health Sciences Institute, Newcastle University, Newcastle upon Tyne, NE2 4AX, UK.ORCID 0000-0003-3426-3717
Mario AbinunImmunity & Inflammation Theme, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, NE2 4HH, UK.ORCID 0000-0002-7050-3565
Amit AllahabadiaAcademic Directorate of Diabetes and Endocrinology, Royal Hallamshire Hospital, Sheffield, S10 2JF, UK.ORCID 0000-0002-1735-4185
Tim BarrattUniversity of Birmingham, Diabetes Unit, Birmingham Children's Hospital, Birmingham, B4 6NH, UK.
Justin H DaviesDepartment of Paediatric Endocrinology, Faculty of Medicine, University of Southampton, University Hospital Southampton NHS Foundation Trust, Southampton, SO16 6YD, UK.ORCID 0000-0001-7560-6320
Paul DimitriThe Department of Paediatric Endocrinology, Sheffield Children's NHS Trust, Western Bank, Sheffield, S10 2TH, UK.ORCID 0000-0001-7625-6713
Amanda DrakeCentre for Cardiovascular Science, Queen's Medical Research Institute, Edinburgh, EH16 4TJ, UK.ORCID 0000-0001-8633-333X
Zainaba MohamedBirmingham Children's Hospital, Birmingham, B46NH, UK.ORCID 0000-0003-1337-7889
Robert D MurrayLeeds Centre for Diabetes and Endocrinology, Leeds Teaching Hospitals NHS Trust, Leeds, LS97TF, UK.ORCID 0000-0001-6730-6109
Caroline A SteeleChildren and Adolescent services, Leeds Teaching Hospitals NHS Trust, UK.ORCID 0000-0003-1785-5761
Nicola ZammittEdinburgh Centre for Endocrinology & Diabetes, Royal Infirmary of Edinburgh, Edinburgh, EH16 4SA, UK.ORCID 0000-0003-1949-3223
Sonya CarnellNewcastle Clinical Trials Unit, Newcastle University, Newcastle upon Tyne, NE2 4AE, UK.ORCID 0000-0002-7648-4297
Jonathan PrichardNewcastle Clinical Trials Unit, Newcastle University, Newcastle upon Tyne, NE2 4AE, UK.
Gillian WatsonNewcastle Clinical Trials Unit, Newcastle University, Newcastle upon Tyne, NE2 4AE, UK.ORCID 0000-0003-2466-0268
Sophie HambletonImmunity & Inflammation Theme, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, NE2 4HH, UK.ORCID 0000-0001-7954-3267
John N S MatthewsPopulation Health Sciences Institute, Newcastle University, Newcastle upon Tyne, NE2 4AX, UK.ORCID 0000-0003-2559-037X
Simon H S PearceTranslational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, International Centre for Life, Newcastle upon Tyne, NE1 3BZ, UK.ORCID 0000-0001-8384-8063

Funding

Medical Research Council G0500783Medical Research Council MR/N006607/1Medical Research Council MR/V005898/1
6 · The paper itself

Abstract

contextRemission rates in young people with Graves hyperthyroidism are less than 25% after 2 years of thionamide antithyroid drug (ATD).

objectiveWe explored whether rituximab (RTX), a B-lymphocyte-depleting agent, would increase remission rates when administered with a short course of ATD.

methodsThis was an open-label, multicenter, single-arm, phase 2 trial in young people (ages, 12-20 years) with Graves hyperthyroidism. An A'Hern design was used to distinguish an encouraging remission rate (40%) from an unacceptable rate (20%). Participants presenting with Graves hyperthyroidism received 500 mg RTX and 12 months of ATD titrated according to thyroid function. ATDs were stopped after 12 months and primary outcome assessed at 24 months. Participants had relapsed at 24 months if thyrotropin was suppressed and free 3,5,3'-triiodothyronine was raised; they had received ATD between months 12 and 24; or they had thyroid surgery/radioiodine.

resultsA total of 27 participants were recruited and completed the trial with no serious side effects linked to treatment. Daily carbimazole dose at 12 months was less than 5 mg in 21 of 27 participants. Thirteen of 27 participants were in remission at 24 months (48%, 90% one-sided CI, 35%-100%); this exceeded the critical value (9) for the A'Hern design and provided evidence of a promising remission rate. B-lymphocyte count at 28 weeks, expressed as a percentage of baseline, was related to likelihood of remission.

conclusionAdjuvant RTX, administered with a 12-month course of ATD, may increase the likelihood of remission in young people with Graves hyperthyroidism. A randomized trial of adjuvant RTX in young people with Graves hyperthyroidism is warranted.

Indexed as

AdolescentAntithyroid AgentsChildDrug Therapy, CombinationFemaleGraves DiseaseHumansImmunoglobulins, Thyroid-StimulatingImmunologic FactorsMalePropylthiouracilRecurrenceRituximabTreatment OutcomeYoung AdultAntithyroid AgentsImmunoglobulins, Thyroid-StimulatingImmunologic FactorsPropylthiouracilRituximabadolescentschildrenGraves diseaserituximabthionamidethyrotoxicosis

Identifiers

PMID34687316
PMCPMC8851941
OpenAlexW3198992726

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.