Kisho is an information platform, not a medical provider. Nothing on this site constitutes medical advice, diagnosis, or treatment recommendations. All content is aggregated from publicly available sources (including ClinicalTrials.gov, PubMed, FDA.gov, and Orphanet) and is provided for informational purposes only. Clinical trial eligibility, treatment decisions, and any health-related actions should always be discussed with a qualified healthcare professional. Kisho does not endorse any specific therapy, organization, or clinical trial. Terms of use · Privacy policy
A myelodysplastic syndrome defined by 5-9% blasts in the bone marrow, and <5% blasts in the blood. Approximately 25% of cases progress to an acute leukemia. (WHO)
Biomarker and diagnostic research for myelodysplastic syndrome with excess blasts-1 has been reported in the published literature.
Estimated prevalence: Unknown (Unknown prevalence).
4 clinical trials registered, 1 recruiting. Interventions under study include drug therapy, other interventions, procedural interventions, and biologic therapy. Pipeline includes 3 PHASE2, 1 PHASE1. Research is primarily sponsored by academic and government institutions.
4 publications have been identified in PubMed for myelodysplastic syndrome with excess blasts-1. Research spans Diagnostic / Biomarker (25%), Review / Meta-Analysis (25%), and Case Report / Case Series (25%).
Koorse Germans S (2026). [PMID: 41720165](https://pubmed.ncbi.nlm.nih.gov/41720165/). *Human pathology*. [Review / Meta-Analysis]
Sicre de Fontbrune F (2026). [PMID: 39159950](https://pubmed.ncbi.nlm.nih.gov/39159950/). *British journal of haematology*. [Clinical Trial Publication]
Eifer M (2025). [PMID: 39978813](https://pubmed.ncbi.nlm.nih.gov/39978813/). *Journal of nuclear medicine : official publication, Society of Nuclear Medicine*. [Case Report / Case Series]
Moore ME (2024). [PMID: 38964162](https://pubmed.ncbi.nlm.nih.gov/38964162/). *Cancer genetics*. [Diagnostic / Biomarker]
Data assembled from 4 of 12 sources · Last updated Sep 20, 2026, 3:09 PM UTC
Program availability and eligibility requirements are set by each foundation. Contact them directly to learn more about your options.
Claim this page and your organization will be listed here for patients and families to find.
European rare disease database
Genetic and Rare Diseases Info Center