Presented in abstract form (oral presentation) at the 45th Annual Meeting of the American Society of Hematology, San Diego, CA, 9 December 2003.
Improved haematopoietic recovery following transplantation with ex vivo-expanded mobilized blood cells†
Article first published online: 20 JUL 2004
DOI: 10.1111/j.1365-2141.2004.05081.x
Additional Information
How to Cite
Miles Prince, H., Simmons, P. J., Whitty, G., Wall, D. P., Barber, L., Toner, G. C., Seymour, J. F., Richardson, G., Mrongovius, R. and Haylock, D. N. (2004), Improved haematopoietic recovery following transplantation with ex vivo-expanded mobilized blood cells. British Journal of Haematology, 126: 536–545. doi: 10.1111/j.1365-2141.2004.05081.x
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Publication History
- Issue published online: 20 JUL 2004
- Article first published online: 20 JUL 2004
- Received 13 April 2004; accepted for publication 26 May 2004
- Abstract
- Article
- References
- Cited By
Keywords:
- ex vivo;
- cell expansion;
- CD34;
- transplantation
Summary
Infusions of ex vivo-expanded (EXE) mobilized blood cells have been explored to enhance haematopoietic recovery following high dose chemotherapy (HDT). However, prior studies have not consistently demonstrated improvements in trilineage haematopoietic recovery. Three cohorts of three patients with breast cancer received three cycles of repetitive HDT supported by either unmanipulated (UM) and/or EXE cells. Efficacy was assessed by an internal comparison of each patient's consecutive HDT cycles, and to 106 historical UM infusions. Twenty-one cycles were supported by EXE cells and six by UM cells alone. Infusions of EXE cells resulted in fewer days with an absolute neutrophil count (ANC) <0·1 × 109/l (median 2 vs. 4 d, P = 0·002) and 3 d faster ANC recovery to >0·1 × 109/l (median 5 vs. 8 d, P = 0·0002). This resulted in a major reduction in the incidence of febrile neutropenia compared with UM cycles (0% vs. 83%; P = 0·008) and in 66% of historical UM cycles (P = 0·01) and a marked reduction in hospital re-admission. There were also fewer platelet transfusions required (43% vs. 100%; P = 0·009). We conclude that EXE cells enhance both neutrophil and platelet recovery and reduce febrile neutropenia, platelet transfusion and hospital re-admission.

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