期刊
PEDIATRIC BLOOD & CANCER
卷 68, 期 11, 页码 -出版社
WILEY
DOI: 10.1002/pbc.29319
关键词
autologous HSCT; G-CSF; hematopoietic stem cell; plerixafor; poor mobilizer
In pediatric solid tumor and lymphoma patients, those with heavily pretreated history may require more frequent dosing of G-CSF or combination with plerixafor for successful HSC mobilization. These methods can effectively improve HSC mobilization in the majority of cases.
Background High-dose chemotherapy with autologous hematopoietic stem cell transplantation (auto-HSCT) is an established treatment for pediatric and young adult patients with solid tumors and lymphomas. Plerixafor is a CXC chemokine receptor type 4 (CXCR4) antagonist that can be used with granulocyte colony stimulating factor (G-CSF) to amplify the mobilization of hematopoietic stem cells (HSCs). Methods We performed a retrospective analysis of 167 pediatric solid tumor and lymphoma patients from January 2010 to July 2020 in whom HSCs were mobilized using G-CSF alone or with plerixafor. Results Thirteen heavily pretreated patients (33.3%) required twice-daily dosing of G-CSF compared to five patients (3.9%) in the not heavily pretreated group (p = .0005). Fourteen heavily pretreated patients (35.9%) required plerixafor compared to four patients (3.1%) in the comparison cohort (p = .0002). The number of mobilization days was similar between both cohorts, with 5 days (range 3-11 days) in the heavily pretreated group and 5 days (range 3-13 days) in the not heavily pretreated group (p = .55). The number of harvest days was 2 days (range 1-5 days) in the heavily pretreated group and 1 day (range 1-4 days) in the not heavily pretreated group (p = .0025). The final cluster of differentiation (CD)34(+)/kilogram (kg) count was 9.52 x 10(6)/kg among heavily pretreated patients compared to 34.99 x 10(6)/kg CD34(+) cells in the comparison group (p < .0001). Three heavily pretreated patients (7.7%) failed HSC mobilization. Conclusions Patients at the highest risk for poor HSC mobilization can be successfully treated with more frequent G-CSF dosing or G-CSF with plerixafor in a large majority of cases.
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