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December 8, 2025BloodOpen Access

Clinical characteristics and molecular profiling of SF3B1-mutated myelodysplastic syndrome (MDS) in a real-world practice

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Authors

RWRoni WangGHGee Fung HowTTTertius Tuy

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Overview

Clinical characteristics and outcomes in SF3B1-mutated MDS patients reveal implications for treatment strategies.

Key Points

  • To describe SF3B1-mutated MDS patients and assess prognostic differences between variants.
  • Retrospective identification of MDS patients with SF3B1 variants via next-generation sequencing.
  • Extraction and amplification of genomic DNA and RNA from bone marrow or blood samples.
  • Evaluation of hematological parameters, mutation profiles, and disease outcomes.
  • Nineteen MDS patients with SF3B1 variants were identified.
  • Ten variants of SF3B1 were found, with K7000E being most prevalent.
  • Patients with more co-mutations had less favorable IPSS-M scores and worse outcomes.

Cite This Study

Wang et al. (2025) studied this question.

synapsesocial.com/papers/69362f6e4fa91c937236e078https://doi.org/10.1182/blood-2025-7402
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