Association between treatment-emergent cytopenias and clinical responses to imetelstat in lower-risk myelodysplastic syndromes - Summary - MDSpire

Association between treatment-emergent cytopenias and clinical responses to imetelstat in lower-risk myelodysplastic syndromes

  • By

  • Amer M. Zeidan

  • Valeria Santini

  • María Díez-Campelo

  • Michael R. Savona

  • Mikkael A. Sekeres

  • Yazan F. Madanat

  • Pierre Fenaux

  • Azra Raza

  • Moshe Mittelman

  • Sylvain Thépot

  • Rena Buckstein

  • Ulrich Germing

  • David Valcárcel

  • Anna Jonášová

  • Sheetal Shah

  • Qi Xia

  • Libo Sun

  • Shyamala Navada

  • Tymara Berry

  • Uwe Platzbecker

  • Rami S. Komrokji

  • April 7, 2026

  • 0 min

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Objective:

To evaluate the association between early treatment-emergent cytopenias with imetelstat and clinical responses in patients with lower-risk myelodysplastic syndromes, highlighting its potential significance.

Key Findings:
  • Significant association between maximum platelet reduction and maximum hemoglobin rise, indicating potential clinical implications.
  • Patients with ≥50% maximum platelet reduction had a higher likelihood of achieving hemoglobin rise ≥1.5 g/dL lasting ≥8 weeks, suggesting a predictive role.
  • Incidence of grade 3/4 neutropenia and thrombocytopenia was high but transient, with low rates of severe clinical consequences, emphasizing the need for monitoring.
Interpretation:

Early cytopenias induced by imetelstat may serve as indicators of clinical response in lower-risk MDS patients, particularly regarding hemoglobin improvement and transfusion independence, with potential applications in clinical practice.

Limitations:
  • Post hoc analysis may introduce bias.
  • Findings are based on a specific patient population from clinical trials, limiting generalizability.
Conclusion:

Early treatment-emergent cytopenias with imetelstat are associated with improved clinical outcomes in lower-risk MDS, suggesting a potential predictive role for these adverse events, warranting close monitoring in clinical settings.

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