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The wider perspective: twenty years of clinical trials in myelodysplastic syndromes.
Duetz, Carolien; Cucchi, David G J; Polak, Tobias B; Janssen, Jeroen J W M; Ossenkoppele, Gert J; Estey, Elihu H; van de Loosdrecht, Arjan A.
Afiliación
  • Duetz C; Department of Hematology, Amsterdam UMC, location VUmc, Vrije Universiteit, Cancer Center Amsterdam, Amsterdam, The Netherlands.
  • Cucchi DGJ; Department of Hematology, Amsterdam UMC, location VUmc, Vrije Universiteit, Cancer Center Amsterdam, Amsterdam, The Netherlands.
  • Polak TB; Department of Biostatistics, Erasmus MC, Rotterdam, The Netherlands.
  • Janssen JJWM; Department of Hematology, Amsterdam UMC, location VUmc, Vrije Universiteit, Cancer Center Amsterdam, Amsterdam, The Netherlands.
  • Ossenkoppele GJ; Department of Hematology, Amsterdam UMC, location VUmc, Vrije Universiteit, Cancer Center Amsterdam, Amsterdam, The Netherlands.
  • Estey EH; Department of Hematology, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
  • van de Loosdrecht AA; Department of Hematology, Amsterdam UMC, location VUmc, Vrije Universiteit, Cancer Center Amsterdam, Amsterdam, The Netherlands.
Br J Haematol ; 196(2): 329-335, 2022 01.
Article en En | MEDLINE | ID: mdl-34632583
ABSTRACT
Most patients with myelodysplastic syndromes (MDS) require therapeutic intervention. However, there are few approved treatments for MDS. To explore reasons, we searched clinicaltrials.gov and clinicaltrialsregister.eu for MDS trials from 2000 to 2020. We assessed which agents were under investigation and analysed clinical trial characteristics and continuation rates from phase I to II to III to approval. As such, we identified 384 unique agents in 426 phase I, 430 phase II and 48 phase III trials. Success rates for phase III trials and agents were low, and MDS trials took markedly longer to complete than the average clinical trial. Although success rates were higher when MDS-specific phase I trials were conducted, 52% of the agents had not been evaluated in a phase I trial for MDS. MDS trials often failed to include quality of life, an especially important outcome for older MDS patients. Our work identifies factors potentially contributing to the paucity of available agents for MDS. We suggest a framework to improve clinical research in MDS that might ultimately augment the number of available agents.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndromes Mielodisplásicos Tipo de estudio: Diagnostic_studies / Etiology_studies / Prognostic_studies / Systematic_reviews Límite: Humans Idioma: En Revista: Br J Haematol Año: 2022 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndromes Mielodisplásicos Tipo de estudio: Diagnostic_studies / Etiology_studies / Prognostic_studies / Systematic_reviews Límite: Humans Idioma: En Revista: Br J Haematol Año: 2022 Tipo del documento: Article País de afiliación: Países Bajos