Peripheral blood stem cell harvesting in young children weighing less than 15 kg

Chih-Ying Lee1, Ting-Yen Yu2, Fen-Lan Lin3

  • 1Division of Pediatric Hematology and Oncology, Department of Pediatrics, Taipei Veterans General Hospital, Taipei, Taiwan; Faculty of Medicine, School of Medicine, National Yang-Ming Chiao-Tung University, Taipei, Taiwan.

Cytotherapy
|May 25, 2024
PubMed

Insights

Collecting stem cells for pediatric cancer patients under 15kg is challenging. A predictive model using preapheresis cell counts and patient factors improves collection success for transplantation.

Area of Science:

  • Pediatric Hematology Oncology
  • Stem Cell Transplantation
  • Cancer Therapeutics

Background:

  • Autologous peripheral blood stem cell (PBSC) transplantation is vital for pediatric cancer treatment.
  • Tandem transplantation offers benefits for specific pediatric malignancies.
  • Collecting sufficient PBSCs in low-body-weight children (<15 kg) presents significant challenges.

Purpose of the Study:

  • To retrospectively analyze the feasibility and outcomes of autologous PBSC collection in pediatric cancer patients weighing less than 15 kg.
  • To identify factors influencing successful stem cell yield for single or tandem transplantation.
  • To develop a predictive model for achieving target stem cell doses.

Main Methods:

  • Retrospective analysis of PBSC collection data from pediatric cancer patients (<15 kg) between April 2006 and August 2021.
  • Collections performed over 2-3 days in the pediatric intensive care unit, aiming for ≥2 × 10^6 CD34+ cells/kg per apheresis.
  • Statistical analysis including correlation of preapheresis hematopoietic progenitor cell (HPC) count with CD34+ yield and development of a predictive model using logistic regression.

Main Results:

  • 129 collections were performed in 40 patients (median age 1.9 years, median weight 11.0 kg).
  • Median CD34+ cell yield was 4.2 × 10^6/kg per apheresis.
  • 78% and 56% of mobilizations achieved sufficient cells for single and tandem transplantation, respectively.
  • Preapheresis HPC count strongly correlated with CD34+ yield (r=0.555, P<0.001).
  • Granulocyte colony-stimulating factor alone was insufficient for mobilization in children ≥2 years.
  • A predictive model combining HPC count (≥20/μL) and factors (age <2 years, no radiation, chemotherapy use) achieved an AUC of 0.787.

Conclusions:

  • Autologous PBSC collection is feasible in pediatric cancer patients <15 kg, with high success rates for single transplantation.
  • Preapheresis HPC count is a key predictor of stem cell yield.
  • A predictive model incorporating patient and treatment factors can enhance the success rate of achieving target stem cell doses for transplantation in this vulnerable population.