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Development of a core outcome set for myelodysplastic syndromes – a Delphi study from the EUMDS Registry Group

Treatment options for myelodysplastic syndromes (MDS) vary widely, depending on the natural disease course and patient‐related factors. Comparison of treatment effectiveness is challenging as different endpoints have been included in clinical trials and outcome reporting. Our goal was to develop the...

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Autores principales: Rochau, Ursula, Stojkov, Igor, Conrads‐Frank, Annette, Borba, Helena H., Koinig, Karin A., Arvandi, Marjan, van Marrewijk, Corine, Garelius, Hege, Germing, Ulrich, Symeonidis, Argiris, Sanz, Guillermo F., Fenaux, Pierre, de Witte, Theo, Efficace, Fabio, Siebert, Uwe, Stauder, Reinhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8221029/
https://www.ncbi.nlm.nih.gov/pubmed/32410281
http://dx.doi.org/10.1111/bjh.16654
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author Rochau, Ursula
Stojkov, Igor
Conrads‐Frank, Annette
Borba, Helena H.
Koinig, Karin A.
Arvandi, Marjan
van Marrewijk, Corine
Garelius, Hege
Germing, Ulrich
Symeonidis, Argiris
Sanz, Guillermo F.
Fenaux, Pierre
de Witte, Theo
Efficace, Fabio
Siebert, Uwe
Stauder, Reinhard
author_facet Rochau, Ursula
Stojkov, Igor
Conrads‐Frank, Annette
Borba, Helena H.
Koinig, Karin A.
Arvandi, Marjan
van Marrewijk, Corine
Garelius, Hege
Germing, Ulrich
Symeonidis, Argiris
Sanz, Guillermo F.
Fenaux, Pierre
de Witte, Theo
Efficace, Fabio
Siebert, Uwe
Stauder, Reinhard
author_sort Rochau, Ursula
collection PubMed
description Treatment options for myelodysplastic syndromes (MDS) vary widely, depending on the natural disease course and patient‐related factors. Comparison of treatment effectiveness is challenging as different endpoints have been included in clinical trials and outcome reporting. Our goal was to develop the first MDS core outcome set (MDS‐COS) defining a minimum set of outcomes that should be reported in future clinical studies. We performed a comprehensive systematic literature review among MDS studies to extract patient‐ and/or clinically relevant outcomes. Clinical experts from the European LeukemiaNet MDS (EUMDS) identified 26 potential MDS core outcomes and participated in a three‐round Delphi survey. After the first survey (56 experts), 15 outcomes met the inclusion criteria and one additional outcome was included. The second round (38 experts) resulted in six included outcomes. In the third round, a final check on plausibility and practicality of the six included outcomes and their definitions was performed. The final MDS‐COS includes: health‐related quality of life, treatment‐related mortality, overall survival, performance status, safety, and haematological improvement. This newly developed MDS‐COS represents the first minimum set of outcomes aiming to enhance comparability across future MDS studies and facilitate a better understanding of treatment effectiveness.
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spelling pubmed-82210292021-06-28 Development of a core outcome set for myelodysplastic syndromes – a Delphi study from the EUMDS Registry Group Rochau, Ursula Stojkov, Igor Conrads‐Frank, Annette Borba, Helena H. Koinig, Karin A. Arvandi, Marjan van Marrewijk, Corine Garelius, Hege Germing, Ulrich Symeonidis, Argiris Sanz, Guillermo F. Fenaux, Pierre de Witte, Theo Efficace, Fabio Siebert, Uwe Stauder, Reinhard Br J Haematol Haematological Malignancy ‐ Clinical Treatment options for myelodysplastic syndromes (MDS) vary widely, depending on the natural disease course and patient‐related factors. Comparison of treatment effectiveness is challenging as different endpoints have been included in clinical trials and outcome reporting. Our goal was to develop the first MDS core outcome set (MDS‐COS) defining a minimum set of outcomes that should be reported in future clinical studies. We performed a comprehensive systematic literature review among MDS studies to extract patient‐ and/or clinically relevant outcomes. Clinical experts from the European LeukemiaNet MDS (EUMDS) identified 26 potential MDS core outcomes and participated in a three‐round Delphi survey. After the first survey (56 experts), 15 outcomes met the inclusion criteria and one additional outcome was included. The second round (38 experts) resulted in six included outcomes. In the third round, a final check on plausibility and practicality of the six included outcomes and their definitions was performed. The final MDS‐COS includes: health‐related quality of life, treatment‐related mortality, overall survival, performance status, safety, and haematological improvement. This newly developed MDS‐COS represents the first minimum set of outcomes aiming to enhance comparability across future MDS studies and facilitate a better understanding of treatment effectiveness. John Wiley and Sons Inc. 2020-05-14 2020-11 /pmc/articles/PMC8221029/ /pubmed/32410281 http://dx.doi.org/10.1111/bjh.16654 Text en © 2020 The Authors. British Journal of Haematology published by British Society for Haematology and John Wiley & Sons Ltd https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Haematological Malignancy ‐ Clinical
Rochau, Ursula
Stojkov, Igor
Conrads‐Frank, Annette
Borba, Helena H.
Koinig, Karin A.
Arvandi, Marjan
van Marrewijk, Corine
Garelius, Hege
Germing, Ulrich
Symeonidis, Argiris
Sanz, Guillermo F.
Fenaux, Pierre
de Witte, Theo
Efficace, Fabio
Siebert, Uwe
Stauder, Reinhard
Development of a core outcome set for myelodysplastic syndromes – a Delphi study from the EUMDS Registry Group
title Development of a core outcome set for myelodysplastic syndromes – a Delphi study from the EUMDS Registry Group
title_full Development of a core outcome set for myelodysplastic syndromes – a Delphi study from the EUMDS Registry Group
title_fullStr Development of a core outcome set for myelodysplastic syndromes – a Delphi study from the EUMDS Registry Group
title_full_unstemmed Development of a core outcome set for myelodysplastic syndromes – a Delphi study from the EUMDS Registry Group
title_short Development of a core outcome set for myelodysplastic syndromes – a Delphi study from the EUMDS Registry Group
title_sort development of a core outcome set for myelodysplastic syndromes – a delphi study from the eumds registry group
topic Haematological Malignancy ‐ Clinical
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8221029/
https://www.ncbi.nlm.nih.gov/pubmed/32410281
http://dx.doi.org/10.1111/bjh.16654
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