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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.
Bone Marrow Transplantation
|March 24, 1998
Summary
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.