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Emulation of the control cohort of a randomized controlled trial in pediatric kidney transplantation with Real-World Data from the CERTAIN Registry

  • Christian Patry
  • , Lukas D. Sauer
  • , Anja Sander
  • , Kai Krupka
  • , Alexander Fichtner
  • , Jolanda Brezinski
  • , Yvonne Geissbühler
  • , Elodie Aubrun
  • , Anna Grinienko
  • , Luca Dello Strologo
  • , Dieter Haffner
  • , Jun Oh
  • , Ryszard Grenda
  • , Lars Pape
  • , Rezan Topaloğlu
  • , Lutz T. Weber
  • , Antonia Bouts
  • , Jon Jin Kim
  • , Agnieszka Prytula
  • , Jens König
  • Mohan Shenoy, Britta Höcker, Burkhard Tönshoff
  • Heidelberg University 
  • Novartis
  • Novartis Pharmaceuticals Corporation
  • IRCCS Ospedale pediatrico Bambino Gesù - Roma
  • Hannover Medical School
  • University of Hamburg
  • Children's Memorial Health Institute
  • University of Duisburg-Essen
  • University of Cologne
  • University of Amsterdam
  • Nottingham University Hospitals NHS Trust
  • Ghent University
  • University of Münster
  • Manchester University NHS Foundation Trust

Research output: Contribution to journalArticlepeer-review

7 Citations (Scopus)

Abstract

Background: Randomized controlled trials in pediatric kidney transplantation are hampered by low incidence and prevalence of kidney failure in children. Real-World Data from patient registries could facilitate the conduct of clinical trials by substituting a control cohort. However, the emulation of a control cohort by registry data in pediatric kidney transplantation has not been investigated so far. Methods: In this multicenter comparative analysis, we emulated the control cohort (n = 54) of an RCT in pediatric kidney transplant patients (CRADLE trial; ClinicalTrials.gov NCT01544491) with data derived from the Cooperative European Paediatric Renal Transplant Initiative (CERTAIN) registry, using the same inclusion and exclusion criteria (CERTAIN cohort, n = 554). Results: Most baseline patient and transplant characteristics were well comparable between both cohorts. At year 1 posttransplant, a composite efficacy failure end point comprising biopsy-proven acute rejection, graft loss or death (5.8% ± 3.3% vs. 7.5% ± 1.1%, P = 0.33), and kidney function (72.5 ± 24.9 vs. 77.3 ± 24.2 mL/min/1.73 m2P = 0.19) did not differ significantly between CRADLE and CERTAIN. Furthermore, the incidence and severity of BPAR (5.6% vs. 7.8%), the degree of proteinuria (20.2 ± 13.9 vs. 30.6 ± 58.4 g/mol, P = 0.15), and the key safety parameters such as occurrence of urinary tract infections (24.1% vs. 15.5%, P = 0.10) were well comparable. Conclusions: In conclusion, usage of Real-World Data from patient registries such as CERTAIN to emulate the control cohort of an RCT is feasible and could facilitate the conduct of clinical trials in pediatric kidney transplantation. Graphical abstract: [Figure not available: see fulltext.].

Original languageEnglish
Pages (from-to)1621-1632
Number of pages12
JournalPediatric Nephrology
Volume38
Issue number5
DOIs
Publication statusPublished - May 2023

Keywords

  • Clinical trial design
  • Emulated cohorts
  • Pediatric kidney transplantation
  • Real-World Data

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