## Abstract We investigated the role of stem cell purification and G‐CSF (early vs. delayed vs. no G‐CSF) administration on hemopoietic recovery and supportive care requirements after stem cell transplantation. Thirty‐two patients submitted to autologous CD34^+^ peripheral blood stem cell transplan
Mobilization effects of G-CSF, GM-CSF, and darbepoetin-α for allogeneic peripheral blood stem cell transplantation
✍ Scribed by Shi Nae Kim; Joon Ho Moon; Jong Gwang Kim; Yee Soo Chae; Yoon Young Cho; Soo Jung Lee; Yun Jeong Kim; Yoo Jin Lee; Jang Soo Suh; Kun Soo Lee; Sang Kyun Sohn
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 170 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0733-2459
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✦ Synopsis
Abstract
The effects of GM‐/G‐CSF and darbepoetin‐α on stem cell mobilization were investigated. From February 2005 to March 2007, 30 allogeneic sibling donors were randomly assigned to a G‐CSF group (5 μg/kg/day for 5–7 days) or triple group (GM‐CSF 10 μg/kg/day on 1st and 2nd day, G‐CSF 5 μg/kg/day for 5–7 days, and darbepoetin‐α 40 mg on 1st day). The MNCs and CD34^+^ cells were not different between the two groups, although the doses (×10^8^/kg of recipient body weight) of CD3^+^ cells (3.64 ± 1.75 vs. 2.63 ± 1.36, P = 0.089) and CD8^+^ cells (1.07 ± 0.53 vs. 0.60 ± 0.30, P = 0.006) were lower in the triple group. The engraftments, frequency of RBC transfusions, and hemoglobin recovery were not different between the two groups. The cumulative incidence of overall and Grades II–IV aGVHD was 64.3% vs. 61.1% and 25.9% vs. 27.1% in the G‐CSF and triple regimen group, respectively, whereas the cumulative incidence of cGVHD was 20.8 ± 1.3% and 24.4 ± 1.7%, respectively. In conclusion, the triple regimen did not seem to be superior to G‐CSF alone in terms of the CD34+ cell dose, hemoglobin recovery, and GVHD. However, the CD8+ cell count was significantly lower in the triple regimen group. The role of a lower CD8+ cell count in the graft may need to be elucidated in the future. J. Clin. Apheresis, 2009. © 2009 Wiley‐Liss, Inc.
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