Autografting with CD34+ peripheral blood stem cells: retained engraftment capability and reduced tumour cell content
Maria Teresa Voso
German Cancer Research Centre, Heidelberg, Germany
Search for more papers by this authorStefan Hohaus
Department of Internal Medicine V, University of Heidelberg,
Search for more papers by this authorMarion Moos
Department of Internal Medicine V, University of Heidelberg,
Search for more papers by this authorMargit Pförsich
Department of Internal Medicine V, University of Heidelberg,
Search for more papers by this authorFriedrich W. Cremer
Department of Internal Medicine V, University of Heidelberg,
Search for more papers by this authorRichard F. Schlenk
Department of Internal Medicine V, University of Heidelberg,
Search for more papers by this authorSimona Martin
Department of Internal Medicine V, University of Heidelberg,
Search for more papers by this authorUte Hegenbart
Department of Internal Medicine V, University of Heidelberg,
Search for more papers by this authorHartmut Goldschmidt
Department of Internal Medicine V, University of Heidelberg,
Search for more papers by this authorRainer Haas
Department of Internal Medicine V, University of Heidelberg,
German Cancer Research Centre, Heidelberg, Germany
Search for more papers by this authorMaria Teresa Voso
German Cancer Research Centre, Heidelberg, Germany
Search for more papers by this authorStefan Hohaus
Department of Internal Medicine V, University of Heidelberg,
Search for more papers by this authorMarion Moos
Department of Internal Medicine V, University of Heidelberg,
Search for more papers by this authorMargit Pförsich
Department of Internal Medicine V, University of Heidelberg,
Search for more papers by this authorFriedrich W. Cremer
Department of Internal Medicine V, University of Heidelberg,
Search for more papers by this authorRichard F. Schlenk
Department of Internal Medicine V, University of Heidelberg,
Search for more papers by this authorSimona Martin
Department of Internal Medicine V, University of Heidelberg,
Search for more papers by this authorUte Hegenbart
Department of Internal Medicine V, University of Heidelberg,
Search for more papers by this authorHartmut Goldschmidt
Department of Internal Medicine V, University of Heidelberg,
Search for more papers by this authorRainer Haas
Department of Internal Medicine V, University of Heidelberg,
German Cancer Research Centre, Heidelberg, Germany
Search for more papers by this authorAbstract
The efficacy of an immunomagnetic purging method and the Isolex 300 devices were assessed for selecting CD34+ cells from leukapheresis products of 29 patients with non-Hodgkin's lymphoma (NHL), 39 with multiple myeloma and 34 with breast cancer. The mean purity of the CD34+ cell population was 93.6% and the mean recovery was 67.7%. Following enzymatic cleavage by chymopapain the expression of Thy-1 and Leu-8 was significantly reduced without affecting haematological recovery. The population of selected CD34+ cells of 4/8 patients with follicular lymphoma became PCR-negative. A 2.5 log reduction of tumour cells could be achieved in four patients with multiple myeloma as shown by a quantitative PCR assay. There were no tumour cells detectable in any of the 19 CD34+ cell preparations of patients with breast cancer. In 64 patients who received 94 cycles of high-dose therapy, a mean number of 4.7 × 106 CD34+ cells/kg were autografted. The time needed for platelet reconstitution was different when a comparison was made with 156 patients, who had received unmanipulated leukapheresis products (10 v 12 d, P = 0.006). No significant differences with regard to neutrophil recovery were noted. Five patients had a graft failure. Two of them died (on day 78 and 88 following PBSCT), and three patients were rescued with unmanipulated back-up transplants. In conclusion, the immunomagnetic selection of CD34+ cells provides autografts with reduced tumour cell content and an engraftment ability similar to that of unmanipulated autografts.
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