ADJUSTMENT OF THE INTERFACE DETECTOR (LOCATION-71) TO THE ABSOLUTE NUMBER OF MONONUCLEAR-CELLS IN THE PERIPHERAL-BLOOD - NO IMPROVEMENT OF THE COLLECTION EFFICIENCY OF THE FENWAL CS3000 PLUS DURING PROGENITOR-CELL HARVESTS

Citation
Jw. Baars et al., ADJUSTMENT OF THE INTERFACE DETECTOR (LOCATION-71) TO THE ABSOLUTE NUMBER OF MONONUCLEAR-CELLS IN THE PERIPHERAL-BLOOD - NO IMPROVEMENT OF THE COLLECTION EFFICIENCY OF THE FENWAL CS3000 PLUS DURING PROGENITOR-CELL HARVESTS, Journal of clinical apheresis, 12(2), 1997, pp. 68-73
Citations number
17
Categorie Soggetti
Hematology
ISSN journal
07332459
Volume
12
Issue
2
Year of publication
1997
Pages
68 - 73
Database
ISI
SICI code
0733-2459(1997)12:2<68:AOTID(>2.0.ZU;2-Y
Abstract
Improvement of the collection efficiency (CE) of the Fenwal CS3000 plu s in collecting circulating progenitor cells (CPC) might diminish the number of leukapheresis procedures (LP) required to obtain the CPC req uired to assure engraftment. We analyzed whether adjustment of the opt ical setting (location 71,L71) to the number of MNC present in the per ipheral blood could enhance the CE of the MNC. Thirty-five patients un derwent 121 LP with an adjusted L71. We compared the results retrospec tively with 26 LP performed with a fixed L71 (1:100) in 12 patients. T he CPC were mobilized with chemotherapy followed by subcutaneous admin istration of granulocyte colony-stimulating factor (G-CSF) in both gro ups. Adjustment of the L71 did neither improve the CE of the MNC, the estimated CE of CD34+ cells nor diminished granulocyte contamination. For the total 121 LP with an adjusted L71 and for the total 26 LP with a fixed L71 the mean CE of MNC were, respectively, 44.6 +/- 18.3% and 46.4 +/- 14%. The mean granulocyte contamination. determined by manua l white blood cell differentiation, was 1.7 +/- 2.3% for the adjusted L71 group and 2.3 +/- 3 for the fixed L71 group. There was no differen ce in the median number of LP required to obtain 3 x 10(6) CD33+ cells /kg between both groups. We found a weak significant correlation betwe en the WBC and pre-LP MNC count and the CE of MNC (r = 0.36, P = 0.012 , resp.r = 0.33, P = 0.023), but no correlation between the CE of MNC and the estimated CE of CD34+ cells (r = 0.24, P = 0.113). In conclusi on, adjustment of the L71 to the MNC did not improve the CE of MNC of the Fenwal CS3000. The lack of correlation between the CE and MNC and the estimated CE of CD34+ cells should be further explored. (C) 1997 W iley-Liss. Inc.