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Published on: September 18, 2011
Delayed G-CSF after autologous progenitor cell transplantation: a prospective randomized trial
B J Bolwell1, B Pohlman, S Andresen
1Department of Hematology and Medical Oncology, Cleveland Clinic Foundation, OH 44195, USA.
Insights
Delaying granulocyte-colony stimulating factor (G-CSF) initiation after autologous progenitor cell transplantation does not impact neutrophil or platelet engraftment times. This finding supports cost savings by allowing later G-CSF administration post-transplant.
Area of Science:
- Hematology
- Oncology
- Transplantation Medicine
Background:
- Granulocyte-colony stimulating factor (G-CSF) is standard post-autologous progenitor cell transplantation to speed neutrophil recovery.
- Current practice often initiates G-CSF on the day of progenitor cell infusion (day 0).
Purpose of the Study:
- To evaluate the impact of initiating G-CSF on day 0, day +3, or day +5 after autologous peripheral blood progenitor cell (PBPC) transplantation on engraftment timelines.
- To assess potential cost savings associated with delayed G-CSF initiation.
Main Methods:
- Prospective, randomized trial involving 70 patients with breast cancer, non-Hodgkin's lymphoma, Hodgkin's disease, or multiple myeloma.
- Patients received chemotherapy-only preparative regimens and PBPC for hematopoietic reconstitution.
- G-CSF initiation was randomized to day 0, day +3, or day +5 post-transplant.
Main Results:
- Neutrophil engraftment occurred at a median of 10 days (day 0 group), 11 days (day +3 group), and 11 days (day +5 group).
- Platelet transfusion independence was achieved at a median of 14 days (day 0), 11 days (day +3), and 14 days (day +5).
- No significant differences in engraftment times were observed between the three G-CSF initiation schedules.
Conclusions:
- Delaying G-CSF initiation up to day +5 after autologous PBPC transplantation does not adversely affect neutrophil or platelet engraftment.
- Delayed G-CSF administration can lead to significant cost savings without compromising patient outcomes.
Abstract:
G-CSF is given after autologous progenitor cell transplantation to accelerate neutrophil engraftment. Historically, G-CSF has been started on the day of progenitor cell infusion. To study the timing of the initiation of G-CSF after autologous peripheral blood progenitor cell (PBPC) transplantation, we conducted a prospective, randomized trial comparing the initiation of G-CSF therapy on day 0, day +3 or day +5 after autologous PBPC transplantation. Seventy patients with diagnoses of breast cancer, non-Hodgkin's lymphoma, Hodgkin's disease, or multiple myeloma were prospectively randomized to one of the three treatment arms. All patients were treated with a chemotherapy (only) preparative regimen. The source of hematopoietic reconstitution was PBPC alone (without autologous marrow), and all patients yielded a minimum of 2 x 10(6) CD34+ cells per kilogram. Times to neutrophil engraftment and platelet engraftment were identical in the three treatment groups, with neutrophil engraftment occurring at a median of 10, 11 and 11 days when starting G-CSF on day 0, day 3 or day 5, respectively. Time to platelet transfusion independence was 14, 11 and 14 days by treatment group. We conclude that delaying the initiation of G-CSF from day 0 to day +5 does not affect engraftment and results in cost savings.
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