Presence of Promyelocytes in Peripheral Blood as a Novel Predictor of Optimal Timing for Single-Step Peripheral Blood Stem Cell Collection

J Nippon Med Sch. 2021 Mar 11;88(1):45-53. doi: 10.1272/jnms.JNMS.2021_88-104. Epub 2020 Mar 31.

Abstract

Background: Because peripheral blood stem cell (PBSC) collection places a burden on the patient and should ideally be completed in a single procedure, a convenient clinical predictive factor is needed.

Methods: This retrospective study included 72 patients who underwent autologous PBSC collection. A median volume of 3.9 × 106 CD34-positive cells/kg (range: 0.3-47.4 × 106 cells/kg) was collected on the first day. We defined failure as inability to collect 2.0 × 106 cells/kg on the first day. PBSC collection was classified as failed (n = 25, 34.7%) and successful (n = 47, 65.3%), and patient clinical characteristics were analyzed.

Results: The success group had significantly more cases in which a differential white blood cell count in peripheral blood on the day of PBSC collection detected promyelocytes (n = 34 [72.3%] vs. n = 11 [44.0%] in the failure group; P = 0.008). Sixty-two patients underwent autologous PBSC transplantation (median number of transplanted cells, 5.6 × 106/μL; range: 1.60-47.4 × 106 cells/μL). Among transplanted patients, the success and failure groups did not significantly differ in relation to the interval until neutrophil, platelet, or red blood cell engraftment.

Conclusion: The presence of promyelocytes in peripheral blood may be a useful indicator of the optimal timing for single-step PBSC collection.

Keywords: malignant lymphoma; multiple myeloma; peripheral blood stem cell transplantation; stem cell collection.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Antigens, CD34
  • Female
  • Granulocyte Precursor Cells*
  • Humans
  • Leukemia, Promyelocytic, Acute / therapy
  • Leukocyte Count
  • Lymphoma / therapy
  • Male
  • Middle Aged
  • Multiple Myeloma / therapy
  • Peripheral Blood Stem Cell Transplantation / methods*
  • Peripheral Blood Stem Cells*
  • Retrospective Studies
  • Time Factors
  • Tissue and Organ Harvesting / methods*
  • Transplantation, Autologous / methods*
  • Young Adult

Substances

  • Antigens, CD34