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Second-line treatment for acute graft-versus-host disease with mesenchymal stromal cells: A decision model.
Thielen, Frederick W; Blommestein, Hedwig M; Oosten, Liesbeth E M; Calkoen, Friso G; Lankester, Arjan C; Zwaginga, Jaap J; Le Blanc, Katarina; Redondo, Alba; Sánchez-Guijo, Fermin; Algeri, Mattia; Locatelli, Franco; Fibbe, Wim E; Uyl-de Groot, Carin A.
Affiliation
  • Thielen FW; Erasmus School of Health Policy and Management, Erasmus University, Rotterdam, The Netherlands.
  • Blommestein HM; Erasmus School of Health Policy and Management, Erasmus University, Rotterdam, The Netherlands.
  • Oosten LEM; Comprehensive Cancer Organisation, Utrecht, The Netherlands.
  • Calkoen FG; Department of Immunohematology and Blood Transfusion, Leiden University Medical Center, Leiden, The Netherlands.
  • Lankester AC; Department of Paediatrics, Leiden University Medical Center, Leiden, The Netherlands.
  • Zwaginga JJ; Department of Paediatrics, Leiden University Medical Center, Leiden, The Netherlands.
  • Le Blanc K; Department of Immunohematology and Blood Transfusion, Leiden University Medical Center, Leiden, The Netherlands.
  • Redondo A; Center for Clinical Transfusion Research, Sanquin Research, Leiden, The Netherlands.
  • Sánchez-Guijo F; Department of Laboratory Medicine, Karolinska Institutet, Stockholm, Sweden.
  • Algeri M; IBSAL-Hospital Universitario de Salamanca, Salamanca, Spain.
  • Locatelli F; IBSAL-Hospital Universitario de Salamanca, Salamanca, Spain.
  • Fibbe WE; Ospedale Pediatrico Bambino Gesù, Rome, Italy.
  • Uyl-de Groot CA; Ospedale Pediatrico Bambino Gesù, Rome, Italy.
Eur J Haematol ; 2018 Aug 06.
Article in En | MEDLINE | ID: mdl-30084111
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.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Health_economic_evaluation / Prognostic_studies Language: En Journal: Eur J Haematol Journal subject: HEMATOLOGIA Year: 2018 Type: Article Affiliation country: Netherlands

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Health_economic_evaluation / Prognostic_studies Language: En Journal: Eur J Haematol Journal subject: HEMATOLOGIA Year: 2018 Type: Article Affiliation country: Netherlands