Risk-Adjusted Comparison of Survival in Chronic Myelomonocytic Leukemia With and Without Allogeneic Stem Cell

Ali Alsugair1, Saubia Fathima1, Mohammad M Alhousani1

  • 1Division of Hematology, Mayo Clinic, Rochester, Minnesota, USA.

Insights

Allogeneic stem cell transplant (ASCT) significantly improves survival for patients with chronic myelomonocytic leukemia (CMML), particularly those in high- and intermediate-risk groups. Early ASCT is recommended, regardless of genetic factors, to overcome adverse prognostic indicators.

Area of Science:

  • Hematology
  • Oncology
  • Stem Cell Transplantation

Background:

  • Chronic myelomonocytic leukemia (CMML) is a heterogeneous myeloid malignancy.
  • The BLAST and BLAST-Mol risk models stratify CMML patients into distinct risk groups.
  • Allogeneic stem cell transplant (ASCT) is a potentially curative option for CMML.

Purpose of the Study:

  • To evaluate the survival impact of ASCT in a large cohort of CMML patients.
  • To assess ASCT's efficacy across different risk strata defined by the BLAST and BLAST-Mol models.
  • To determine if ASCT can overcome adverse prognostic factors in CMML.

Main Methods:

  • Retrospective analysis of 775 consecutive CMML patients from Mayo Clinic.
  • Comparison of overall survival (OS) between patients who underwent ASCT and those who did not.
  • Survival analysis adjusted for baseline BLAST clinical and BLAST-Mol risk categories using time-dependent Cox models.

Main Results:

  • ASCT was associated with significantly longer median OS (77 vs. 28 months; p < 0.01).
  • This survival benefit was maintained after adjusting for BLAST and BLAST-Mol risk categories across high-, intermediate-, and low-risk groups.
  • Time-dependent Cox models confirmed ASCT's favorable impact on survival for high- and intermediate-risk CMML patients.

Conclusions:

  • ASCT provides a significant survival advantage for CMML patients, especially those in high- and intermediate-risk groups.
  • ASCT can mitigate the negative prognostic impact of certain high-risk cytogenetic or molecular abnormalities.
  • These findings support the consideration of early ASCT in CMML management, irrespective of genetic profile.