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Updated: Apr 15, 2026

Phenotypic Analysis and Isolation of Murine Hematopoietic Stem Cells and Lineage-committed Progenitors
Published on: July 8, 2012
Hematopoietic progenitor cells collection in pediatric patients with brain tumor
Ana Spínola1, Sara Ferreira1, Fátima Amado1
1Serviço De Terapia Celular, Instituto Português De Oncologia Do Porto Francisco Gentil, EPE, Porto, Portugal.
Insights
Hematopoietic progenitor cell (HPC) collection via leukapheresis is safe and effective in pediatric brain tumor patients. This outpatient procedure yields sufficient cells for aggressive chemotherapy, potentially improving outcomes.
Area of Science:
- Pediatric Oncology
- Hematology
- Cellular Therapy
Background:
- Brain tumors are a significant concern in pediatric oncology.
- Hematopoietic progenitor cell (HPC) transplantation is a critical supportive care measure.
- Leukapheresis is a method for collecting HPCs.
Purpose of the Study:
- To evaluate the efficacy and safety of leukapheresis for HPC collection in pediatric brain tumor patients.
- To determine the feasibility of collecting adequate HPCs for potential autologous transplantation.
Main Methods:
- Retrospective analysis of 19 pediatric patients (median age 5 years) with brain tumors undergoing leukapheresis.
- Mobilization with G-CSF, with or without chemotherapy, followed by leukapheresis using COBE® Spectra or Spectra Optia®.
- Use of ACD-A anticoagulant, with red blood cell priming for younger children.
Main Results:
- Successful HPC collection was achieved in all 19 patients, with a median of 4.6 × 10^6 CD34+ cells/Kg collected.
- A median of 1.5 leukapheresis procedures per patient were performed.
- 12 children proceeded to tandem transplantation, indicating sufficient cell yield.
Conclusions:
- Leukapheresis is an efficient and well-tolerated outpatient procedure for HPC collection in pediatric brain tumor patients.
- Modern mobilization strategies and apheresis technology enable high HPC yields.
- This facilitates the use of intensive chemotherapy regimens to improve patient prognoses.
Aim:
To analyze the efficacy and safety of hematopoietic progenitor cells (HPC) collections by leukapheresis in pediatric patients with brain tumors.
Results:
Between 2003 and 2014, we collected HPC from 19 children (12 boys/7 girls), median age at the diagnosis of 5 years old (<1-15 years old) and weight of 16.8 Kg (6.7-42). Diagnoses were Medulloblastoma (n = 10), Primitive Neuroectodermal Tumor (n = 5), Atypical Teratoid Rhabdoid Tumor (n = 3) and Secreting Germ Cell Tumor (n = 1). All patients performed leukapheresis by a central venous catheter, at the fifth day of mobilization with G-CSF (median dose 11.7 µg/Kg/day), 9 of them with COBE® Spectra and 10 with Spectra Optia®. The anticoagulant used was ACD-A, ratio of 14:1 or ACD-A plus heparin, ratio 25:1. The tubing set was primed with a compatible, irradiated, leukodepleted and hematocrit adjusted packed red cells for all children <30 kg (n = 17). A median of 1.5 (1-3) leukapheresis per patient was performed with an average of 3 (1.5-5.4) blood volumes processed; 3 children did a second mobilization and one additional leukapheresis. The median number of CD34+ cells collected was 4.6 × 10(6) /Kg (0.18-22.6) of patient body weight; 12 children collected for a tandem transplant. The median time between cell collection and infusion was 3 (0.6-9.1) months.
Conclusions:
HPC collection in children is an efficient and well tolerated technique, performed as an outpatient procedure. With the new mobilization schemes and leukapheresis technology, we can collect a high number of HPC allowing pediatric oncologist to establish more aggressive chemotherapy protocols hoping to improve patient outcome.
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