AI Article Synopsis

  • Myelodysplastic syndromes (MDS) are complex blood disorders marked by ineffective blood cell production, leading to lower blood cell counts and a higher chance of progressing to acute leukemia.
  • The MDS International Working Group (IWG) created response criteria in 2000 to measure treatment effectiveness, but issues with these criteria have affected clinical trial success and the correlation with patient outcomes.
  • Recent updates in the IWG criteria (most notably in 2023) aim to clarify definitions and improve the consistency of response assessment, focusing on meaningful patient-centered outcomes in higher-risk MDS cases.

Article Abstract

Myelodysplastic syndromes/neoplasms (MDS) are heterogeneous, clonal myeloid neoplasms characterized by ineffective hematopoiesis, progressive cytopenias, and an increased risk of progression to acute myeloid leukemia. The diversity in disease severity, morphology, and genetic landscape challenges not only novel drug development but also therapeutic response assessment. The MDS International Working Group (IWG) response criteria were first published in the year 2000 focusing on measures of blast burden reduction and hematologic recovery. Despite revision of the IWG criteria in 2006, correlation between IWG-defined responses and patient-focused outcomes, including long-term benefits, remains limited and has potentially contributed to failures of several phase III clinical trials. Several IWG 2006 criteria also lacked clear definitions leading to problems in practical applications and interobserver and intraobserver consistency of response reporting. Although the 2018 revision addressed lower-risk MDS, the most recent update in 2023 redefined responses for higher-risk MDS and has set out to provide clear definitions to enhance consistency while focusing on clinically meaningful outcomes and patient-centered responses. In this review, we analyze the evolution of the MDS response criteria, limitations, and areas of improvement.

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http://dx.doi.org/10.1097/PPO.0000000000000666DOI Listing

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