TY - JOUR
T1 - The wider perspective
T2 - twenty years of clinical trials in myelodysplastic syndromes
AU - Duetz, Carolien
AU - Cucchi, David G. J.
AU - Polak, Tobias B.
AU - Janssen, Jeroen J. W. M.
AU - Ossenkoppele, Gert J.
AU - Estey, Elihu H.
AU - van de Loosdrecht, Arjan A.
N1 - Publisher Copyright: © 2021 The Authors. British Journal of Haematology published by British Society for Haematology and John Wiley & Sons Ltd. Copyright: Copyright 2021 Elsevier B.V., All rights reserved.
PY - 2022/1
Y1 - 2022/1
N2 - 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.
AB - 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.
KW - clinical trials
KW - drug development
KW - myelodysplastic syndromes
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85116747405&origin=inward
UR - https://www.ncbi.nlm.nih.gov/pubmed/34632583
U2 - https://doi.org/10.1111/bjh.17892
DO - https://doi.org/10.1111/bjh.17892
M3 - Comment/Letter to the editor
C2 - 34632583
SN - 0007-1048
VL - 196
SP - 329
EP - 335
JO - British journal of haematology
JF - British journal of haematology
IS - 2
ER -