4.2 Article

Transplantation of highly purified CD34(+)Thy-I+ hematopoietic stem cells in patients with metastatic breast cancer

Journal

BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION
Volume 6, Issue 3, Pages 262-271

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/S1083-8791(00)70008-5

Keywords

stem cells; transplantation; breast cancer; tumor purging

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We report here the transplantation of extensively purified mobilized peripheral blood CD34(+)Thy-1(+) hematopoietic stem cells from 22 patients with recurrent or metastatic breast cancer. patients were mobilized with either high-dose granulocyte colony-stimulating factor (G-CSF) alone or cyclophosphamide plus G-CSF. Median purity of the stem cell product at cryopreservation was 95.3% (range, 91.1%-98.3%), and viability was 98.6% (range, 96.5%-100%). After high-dose chemotherapy with carmustine, cisplatin, and cyclophosphamide, CD34(+)Thy-1(+) cells at a median dose of 11.3 x 10(5) per kilogram (range, 4.7-163 x 10(5) per kilogram) were infused. No infusion-related toxicity was observed. Neutrophil recovery was prompt, with median absolute neutrophil count >500/muL by day 10 (range, 8-15 days) and >1000/muL by day 11 (range, 8-17 days). Median platelet recovery (>20,000/muL) was observed by day 14 (range, 9-42 days) and >50,000/muL, by day 17 (range, 11-49 days). Tumor cell depletion below the limits of detection of a sensitive immunofluorescence-based assay was accomplished in all patients who had detectable tumor cells in apheresis products before processing. Although CD4(+) T-cell reconstitution was slow, no unusual infections were observed. Neither early nor late graft failure was observed, and no patient required infusion of unmanipulated backup cells. At a median follow-up of approximately 1.4 years and a maximum follow-up of 2.5 years, 16 of the 22 patients remain alive, with 9 free of disease progression, and have stable blood counts. In summary, highly purified CD34(+)Thy-1(+) cells used as the sole source of the hematopoietic graft result in rapid and sustained hematopoietic engraftment.

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