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Second-line treatment for acute graft-versus-host disease with mesenchymal stromal cells: A decision model

  • Frederick W. Thielen*
  • , Hedwig M. Blommestein
  • , Liesbeth E. M. Oosten
  • , Friso G. Calkoen
  • , Arjan C. Lankester
  • , Jaap J. Zwaginga
  • , Katarina le Blanc
  • , Alba Redondo
  • , Fermin Sánchez-Guijo
  • , Mattia Algeri
  • , Franco Locatelli
  • , Wim E. Fibbe
  • , Carin A. Uyl-de Groot
  • *Corresponding author for this work
  • Erasmus School of Health Policy & Management
  • The Netherlands Comprehensive Cancer Organisation, P.O. Box 19079, 3501 DB Utrecht, the Netherlands
  • Leiden University Medical Center
  • Sanquin Blood Supply Foundation
  • Karolinska Institutet
  • Hospital Clínico Universitario de Salamanca
  • IRCCS Ospedale pediatrico Bambino Gesù - Roma

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

Objective: No standard second-line treatment exists for acute graft-versus-host disease steroid-refractory (SR-aGvHD), and long-term outcomes remain poor. Mesenchymal stromal cells (MSCs) have been evaluated as treatment, but no disease model (DM) exists that integrates and extrapolates currently available evidence. The aim of this study was to develop such a DM to describe the natural history of SR-aGvHD and to predict long-term outcomes. Method: The DM was developed in collaboration with experts in haematology-oncology. Subsequently, a model simulation was run. Input parameters for transition and survival estimates were informed by published data of clinical trials on MSC treatment for SR-aGvHD. Parametric distributions were used to estimate long-term survival rates after MSCs. Results: The newly developed DM is a cohort model that consists of eight health states. For the model simulation, we obtained data on 327 patients from 14 published phase II trials. Due to limited evidence, DM structure was simplified and several assumptions had to be made. Median overall survival was 3.2 years for complete response and 0.5 years for no complete response. Conclusion: The DM provides a comprehensive overview on the second-line treatment pathway for aGvHD and enables long-term predictions that can be used to perform a cost-effectiveness analysis comparing any treatment for SR-aGvHD.
Original languageEnglish
Pages (from-to)676-683
JournalEuropean journal of haematology
Volume101
Issue number5
DOIs
Publication statusPublished - 1 Nov 2018
Externally publishedYes

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