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Autologous peripheral blood progenitor cell transplantation
1Division of Hematologic Malignancies, Dana-Farber Cancer Institute, Boston, MA 02115, USA.
Journal of Clinical Apheresis
|January 1, 1995
Summary
Peripheral blood stem cell (PBSC) harvesting uses apheresis technology for faster engraftment post-chemotherapy. CD34+ cell counts predict stem cell engraftment potential, guiding high-dose therapy for various cancers.
Area of Science:
- Hematology
- Oncology
- Stem Cell Transplantation
Background:
- Autologous peripheral blood stem cell (PBSC) collection is crucial for high-dose chemotherapy regimens.
- Recombinant growth factors, like granulocyte (G)-CSF or granulocyte-macrophage (GM)-CSF, enhance PBSC mobilization.
- Apheresis should ideally occur before significant stem cell toxicity from agents like alkylating agents.
Purpose of the Study:
- To review the current strategies and technologies for harvesting autologous PBSCs.
- To discuss the role of CD34+ cell enumeration as a surrogate marker for stem cell engraftment.
- To explore challenges and future directions in PBSC transplantation.
Main Methods:
- Utilizes efficient apheresis technology for PBSC collection.
- Employs recombinant growth factors (G-CSF/GM-CSF) to stimulate stem cell release.
- Relies on CD34+ cell enumeration to assess stem cell potency and predict engraftment.
Main Results:
- High-dose chemoradiotherapy with PBSC rescue leads to faster engraftment than bone marrow transplantation (BMT).
- CD34+ cell count serves as a reliable index for long-term hematopoietic reconstitution.
- Tumor cell contamination in mobilized PBSCs is a concern, with ongoing research into purification methods.
Conclusions:
- Autologous PBSC transplantation is an effective strategy for treating malignancies, offering rapid engraftment.
- CD34+ cell enumeration is vital for guiding stem cell collection and transplantation protocols.
- Future research focuses on ex vivo expansion, alternative stem cell sources, and gene therapy for enhanced outcomes.