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Increase in circulating stem cells following chemotherapy in man
Blood
|June 1, 1976
Summary
Cancer patients undergoing chemotherapy show increased circulating granulocytic stem cells (CFU-C) post-treatment. Peripheral blood stem cell collection via leukopheresis is feasible for autologous infusion to mitigate myelosuppression.
Area of Science:
- Hematology
- Oncology
- Stem Cell Biology
Background:
- Chemotherapy often leads to myelosuppression, impacting cancer patient recovery.
- Granulocytic stem cells, or colony-forming units-culture (CFU-C), are crucial for hematopoiesis.
- Assessing CFU-C levels is vital for understanding treatment effects and recovery potential.
Purpose of the Study:
- To quantify circulating granulocytic stem cells (CFU-C) in cancer patients during intermittent chemotherapy.
- To evaluate the feasibility of collecting and cryopreserving peripheral blood stem cells.
- To explore the potential of autologous stem cell infusion for managing chemotherapy-induced myelosuppression.
Main Methods:
- In vitro methylcellulose technique used to determine CFU-C concentration.
- Leukopheresis employed for large-scale stem cell collection from peripheral blood.
- Cryopreservation methods assessed for stem cell recovery efficacy.
- Serial monitoring of CFU-C levels during chemotherapy cycles.
Main Results:
- Post-treatment CFU-C median concentration (23) was significantly higher than pre-treatment (6) in cancer patients (p < 0.001).
- Leukopheresis and cryopreservation achieved a high median CFU-C recovery rate of 99.5%.
- Cyclical increases in stem cell concentration, up to 20 times baseline, were observed.
- Peripheral blood apheresis can yield stem cell quantities comparable to bone marrow harvests.
Conclusions:
- Intermittent chemotherapy significantly mobilizes granulocytic stem cells into the peripheral circulation.
- Peripheral blood stem cell collection is an effective method for obtaining substantial numbers of CFU-C.
- Autologous stem cell infusion using mobilized peripheral blood stem cells is a potentially practical strategy to prevent myelosuppression in intensive chemotherapy regimens.