Mini-ICE effectively mobilises peripheral blood stem cells after fludarabine-based regimens in acute myeloid

Anna Mele1, Giuliana Leopardi, Giovanni Sparaventi

  • 1Department of Haematology, Hospital San Salvatore, Pesaro, Italy.

Insights

A low-dose Mini-ICE regimen effectively mobilizes and collects peripheral blood stem cells (PBSC) in acute myeloid leukemia (AML) patients after fludarabine treatment. This approach aids autologous PBSC transplantation in heavily pretreated cases.

Area of Science:

  • Hematology
  • Oncology
  • Stem Cell Transplantation

Background:

  • Fludarabine-based chemotherapy regimens significantly impair peripheral blood stem cell (PBSC) mobilization and collection in acute myeloid leukemia (AML) patients.
  • This impairment poses a challenge for autologous PBSC transplantation, limiting therapeutic options for heavily pretreated individuals.

Purpose of the Study:

  • To evaluate the efficacy of a low-dose 5-day Mini-ICE regimen in reversing the negative effects of fludarabine on PBSC mobilization and collection.
  • To assess the feasibility and tolerability of the Mini-ICE regimen in adult AML patients previously treated with fludarabine.

Main Methods:

  • Seven adult AML patients who received fludarabine-based regimens were treated with a low-dose 5-day Mini-ICE regimen (oral idarubicin and etoposide; subcutaneous cytosine arabinoside).
  • Leukapheresis was initiated when CD34+ cell counts exceeded 10/microL.
  • Collected PBSC were used for autologous transplantation.

Main Results:

  • The Mini-ICE regimen successfully mobilized and collected a median of 8.1 x 10(6) CD34+ cells/kg.
  • All patients underwent successful autologous PBSC transplantation.
  • Patients experienced rapid neutrophil and platelet recovery with normal transfusional support.

Conclusions:

  • The low-dose Mini-ICE regimen is a feasible, well-tolerated, and effective strategy for PBSC mobilization and collection in AML patients with low yields after fludarabine treatment.
  • This approach may expand therapeutic options for autologous PBSC transplantation in heavily pretreated hematological malignancies.

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