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Updated: Sep 29, 2026

Proliferation and Differentiation of Murine Myeloid Precursor 32D/G-CSF-R Cells
Published on: February 21, 2018
Granulocyte colony-stimulating factor alone at 12 microg/kg twice a day for 4 days for peripheral blood progenitor
J Sevilla1, M González-Vicent, L Madero
1Hospital Infantil Universitario Niño Jesús, Madrid, Spain.
Insights
This study shows a G-CSF mobilization schedule safely and effectively collects progenitor cells in children. Most pediatric patients achieved the target CD34(+) cell dose in a single leukapheresis procedure.
Area of Science:
- Pediatric Hematology
- Stem Cell Transplantation
- Cellular Therapy
Background:
- Optimizing peripheral blood progenitor cell (PBPC) collection in children is crucial for hematopoietic stem cell transplantation.
- Current mobilization strategies require refinement for improved efficiency and safety in pediatric populations.
Purpose of the Study:
- To evaluate a mobilization schedule using high-dose, twice-daily G-CSF for 4 days in pediatric patients.
- To assess the safety and efficacy of this G-CSF regimen for PBPC collection.
Main Methods:
- A mobilization schedule involving G-CSF (12 microg/kg twice daily) for 4 days was administered to pediatric patients.
- Peripheral blood progenitor cells (PBPCs) were collected via large volume leukapheresis.
- Toxicity associated with G-CSF was monitored.
Main Results:
- The median CD34(+) cell yield was 4.4 x 10(6)/kg body weight.
- 83.6% of patients (46 out of 55) achieved the target dose of ≥2 x 10(6) CD34(+) cells/kg body weight after a single leukapheresis.
- Mild G-CSF-related toxicities (bone pain, myalgia) were observed in 23% of patients.
Conclusions:
- The studied G-CSF mobilization schedule is safe and effective for collecting PBPCs in most pediatric patients.
- A single large volume leukapheresis is sufficient to achieve the minimum target CD34(+) cell dose.
- This regimen offers an efficient approach to PBPC collection in pediatric settings.
Abstract:
In children, the optimal mobilization schedule for harvesting peripheral blood progenitor cells (PBPC) is an issue of continuous research. We have studied a schedule based on high and daily divided doses of G-CSF (12 microg/kg body weight twice daily) for 4 days for PBPC priming. Toxicity related to G-CSF was observed in 13 patients (23%), mainly mild bone pain and myalgia. The median CD34(+)cell number collected was 4.4 (0.4-35 x 10(6)/kg body weight), with 46 patients achieving 2 x 10(6)/kg body weight (83.6%) after a single large volume leukapheresis. In conclusion, this mobilization schedule allows safe and efficient collection of the minimum target CD34(+) cell dose in most pediatric patients by only one procedure.
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Differentiation of Common Myeloid Progenitor Cells
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