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Dangosydd eitem ddigidol (DOI)

  • Paul A. Brogan
    Great Ormond Street Hospital, London
  • B. Arch
    Department of Molecular and Clinical Pharmacology, University of Liverpool
  • H. Hickey
    Department of Molecular and Clinical Pharmacology, University of Liverpool
  • J. Anton
    Sant Joan de Déu Hospital, Barcelona
  • E. Iglesias
    Sant Joan de Déu Hospital, Barcelona
  • E, Baildam
    Alder Hey Children's NHS Foundation Trust, Liverpool
  • K. Mahmood
    Alder Hey Children's NHS Foundation Trust, Liverpool
  • G. Cleary
    Alder Hey Children's NHS Foundation Trust, Liverpool
  • E. Moraitis
    Great Ormond Street Hospital, London
  • C. Papadopoulou
    Great Ormond Street Hospital, London
  • M.W. Beresford
    Department of Molecular and Clinical Pharmacology, University of Liverpool
  • P. Riley
    Royal Manchester Children’s Hospital
  • S. Demir
    Hacettepe University
  • S. Ozen
    Hacettepe University
  • Giovanna Culeddu
  • Dyfrig Hughes
  • P. Dolezalova
    Charles University Prague
  • L. Hampson
    Lancaster University
  • J. Whitehead
    Lancaster University
  • D. Jayne
    University of Cambridge
  • N. Ruperto
    UOSID Centro Trial, Genova
  • Catrin Tudor-Smith
    Department of Molecular and Clinical Pharmacology, University of Liverpool
  • D. Eleftheriou
    Great Ormond Street Hospital, London
Objective
Cyclophosphamide (CYC) is used in clinical practice off-label for induction of remission of childhood polyarteritis nodosa (cPAN). Mycophenolate mofetil (MMF) might offer a less toxic alternative: we explored their relative effectiveness in a randomised controlled trial (RCT).
Methods
International, open-label, Bayesian, RCT investigating the relative effectiveness of MMF and CYC for remission induction in cPAN. Eleven newly-diagnosed patients were randomised (1:1) to MMF or intravenous-CYC; all received the same glucocorticoid regimen. The primary endpoint was remission within 6-months whilst compliant with glucocorticoid taper. Bayesian distributions for remission rates were established a priori for MMF and CYC by experienced clinicians, and updated to posterior distributions on trial completion.
Results
Baseline disease activity/features were similar between groups. The primary remission endpoint occurred in 4/6 patients (67%) in the MMF group and 4/5 patients (80%) in the CYC group. Time to remission was shorter in the MMF group (median 7.4 weeks versus 17.5 weeks for CYC). No relapses occurred in either group within 18-months. Two serious infections were probably related to MMF. Physical and psychosocial quality-of-life scores were superior in the MMF group compared to CYC at 6-and 18-months. Combining the prior expert opinion with results from MYPAN provided posterior estimates of remission of 71% (90% CrI 51-83%) for MMF; and 75% (90% CrI 57-86%) for CYC.
Conclusion
Taking the prior opinion and the study results together, rates of remission induction in cPAN on MMF and CYC are similar, and MMF might be associated with better health-related quality of life than CYC.

Allweddeiriau

Iaith wreiddiolSaesneg
Tudalennau (o-i)1673-1682
CyfnodolynArthritis and Rheumatology
Cyfrol73
Rhif y cyfnodolyn9
Dyddiad ar-lein cynnar24 Maw 2021
Dynodwyr Gwrthrych Digidol (DOIs)
StatwsCyhoeddwyd - Medi 2021

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