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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...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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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. |
format | Online Article Text |
id | pubmed-8221029 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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