Intensive cyclic chemotherapy with unprocessed whole blood support in advanced breast cancer
Language English Country Slovakia Media print
Document type Clinical Trial, Comparative Study, Journal Article, Research Support, Non-U.S. Gov't
PubMed
11327535
Knihovny.cz E-resources
- MeSH
- Chemotherapy, Adjuvant MeSH
- Cyclophosphamide administration & dosage MeSH
- Adult MeSH
- Epirubicin administration & dosage MeSH
- Granulocyte Colony-Stimulating Factor administration & dosage MeSH
- Blood Transfusion * MeSH
- Cryopreservation MeSH
- Leukapheresis MeSH
- Leukopenia chemically induced prevention & control MeSH
- Middle Aged MeSH
- Humans MeSH
- Breast Neoplasms drug therapy therapy MeSH
- Antineoplastic Combined Chemotherapy Protocols adverse effects therapeutic use MeSH
- Hematopoietic Stem Cell Transplantation * MeSH
- Thrombocytopenia chemically induced prevention & control MeSH
- Dose-Response Relationship, Drug MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Clinical Trial MeSH
- Research Support, Non-U.S. Gov't MeSH
- Comparative Study MeSH
- Names of Substances
- Cyclophosphamide MeSH
- Epirubicin MeSH
- Granulocyte Colony-Stimulating Factor MeSH
The aim of our project was to compare the efficacy of mobilised whole blood versus cryopreserved PBPC (peripheral blood progenitor cells) obtained by leukapheresis in the support of hematopoietic recovery in cyclic intensive chemotherapy. Twenty-nine women with breast carcinoma were treated. The mean age was 46 years. In stage III were 23, in stage IV were 6. They received 6 cycles of epirubicin 150 mg/m2 and cyclophosphamide 1250 mg/m2. In the first cycle, 24 hours after chemotherapy, application of G-CSF 5 microg/kg/day was started, and discontinued when leukaphereses and whole blood collections were done. Leukapheresed progenitors were then divided into 3 aliquots, cryopreserved and reinfused after the 4th, 5th and 6th chemotherapy cycles. Mobilised whole blood was collected on day 14 of the 1st and 2nd cycles and reinfused 24 hours after chemotherapy. The occurrence of grade IV leukopenia was 1.82 times higher with whole blood support and grade IV thrombocytopenia 2.64 times higher than in cycles with cryopreserved PBPC support. This resulted from the fact that in one application the numbers of CD34+ cells and CFU-GM were nearly double in cryoconcentrates. The yields of CD34+ cells in 450 ml of whole blood were 1.8 x 10(6)/kg, which is not sufficient for optimal hemopoietic recovery.