Impact of apheresis automation on procedure quality and predictability of CD34+ cell yield

被引:4
作者
Besson, Nelly [1 ]
Bruun, Mie Topholm [2 ]
Larsen, Thomas Stauffer [3 ]
Nielsen, Christian [2 ]
机构
[1] Med Affairs Dept Terumo BCT, Zaventem, Belgium
[2] Odense Univ Hosp, Dept Clin Immunol, JP Winslows Vej 4, DK-5000 Odense C, Denmark
[3] Odense Univ Hosp, Dept Haematol, Odense, Denmark
关键词
CD34(+)cells; hematopoietic stem cells; spectra optia; PERIPHERAL-BLOOD; PROGENITOR CELLS; COLLECTION; EFFICIENCY; TRANSPLANTATION; LEUKAPHERESIS; MOBILIZATION; VALIDATION; PREDICTION; COUNTS;
D O I
10.1002/jca.21625
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Success of peripheral blood stem cell (PBSC) collections depends on patient biological parameters and stable apheresis device performance. We investigated product quality and factors influencing main apheresis procedure outcomes including CD34(+) collection efficiency (CE), product volume or platelet CE. We also assessed different CD34(+) cell yield prediction algorithms. Autologous PBSC collections by Spectra Optia from myeloma and lymphoma patients were analyzed. Complete blood count (CBC) from patient preprocedure and from collected products were assessed. (1) Product yield was calculated, (2) Product CBC was correlated with patient preprocedure variables, and (3) Predictions of CD34(+) yields based on (a) product CD34(+) cell concentration in samples after two or four chamber flushes or (b) traditional CE2 benchmark, were compared. 62 procedures in 41 patients were analyzed. 84% of all procedures were run without operator intervention. Median CD34(+) CE2 was 56.9% (48.8%-65.2%) and quite stable irrespective of patient conditions, with minor influence from patient white blood cell (WBC) precounts (r(s)=-.47; P<.001). Platelet loss correlated with WBC precount (r(s)=.46; P<.001), product volume (r(s)=.71; P<.0001) and number of chambers collected (r(s)=.72; P<.0001). CD34(+) cell yield was better predicted based on (a) product CD34(+) cell concentration from samples after 2 and 4 chamber flushes, respectively (r(s)=.969; P<.0001 and r(s)=.9648; P<.0001) than based on (b) CE2 formula (r(s)=.8262, P<.0001). Spectra Optia provides good quality PBSC products with stable and predictable yield regardless of starting conditions. CD34(+) sampling of product after few chamber flushes could be used to predict CD34(+) yield.
引用
收藏
页码:494 / 504
页数:11
相关论文
共 21 条
[1]   CD34 counts to predict the adequate collection of peripheral blood progenitor cells [J].
Armitage, S ;
Hargreaves, R ;
Samson, D ;
Brennan, M ;
Kanfer, E ;
Navarrete, C .
BONE MARROW TRANSPLANTATION, 1997, 20 (07) :587-591
[2]   Mobilized allogeneic peripheral stem/progenitor cell apheresis with Spectra Optia v.5.0, a novel, automatic interface-controlled apheresis system: results from the first feasibility trial [J].
Brauninger, S. ;
Bialleck, H. ;
Thorausch, K. ;
Seifried, E. ;
Bonig, H. .
VOX SANGUINIS, 2011, 101 (03) :237-246
[3]   Allogeneic donor peripheral blood "stem cell" apheresis: prospective comparison of two apheresis systems [J].
Brauninger, Susanne ;
Bialleck, Heike ;
Thorausch, Kristin ;
Felt, Tom ;
Seifried, Erhard ;
Bonig, Halvard .
TRANSFUSION, 2012, 52 (05) :1137-1145
[4]   A prospective randomized trial of two popular mononuclear cell collection sets for autologous peripheral blood stem cell collection in multiple myeloma [J].
Cooling, Laura ;
Hoffmann, Sandra ;
Herrst, Michelle ;
Muck, Charles ;
Armelagos, Heidi ;
Davenport, Robertson .
TRANSFUSION, 2010, 50 (01) :100-119
[5]   HPC-A Dose Prediction on the Optia® Cell Separator Based on a Benchmark CE2 Collection Efficiency: Promoting Clinical Efficiency, Minimizing Toxicity, and Allowing Quality Control [J].
Cousins, Antony F. ;
Sinclair, Joy E. ;
Alcorn, Michael J. ;
Green, Rachel H. A. ;
Douglas, Kenny W. .
JOURNAL OF CLINICAL APHERESIS, 2015, 30 (06) :321-328
[6]   Monitoring of CD34+ cells during leukapheresis allows a single, successful collection of hemopoietic progenitors in patients with low numbers of circulating stem cells [J].
de Fabritiis, P ;
Gonzalez, M ;
Meloni, G ;
De Propris, MS ;
Bellucci, R ;
Cordone, I ;
Gozzer, M ;
Leone, G ;
Mandelli, F .
BONE MARROW TRANSPLANTATION, 1999, 23 (12) :1229-1236
[7]   Peripheral blood stem cell collection: The interaction of technology, procedure, and biological factors [J].
Hester, J .
TRANSFUSION SCIENCE, 2000, 23 (02) :125-132
[8]   Peripheral blood stem cell yield calculated using preapheresis absolute CD34+cell count, peripheral blood volume processed, and donor body weight accurately predicts actual yield at multiple centers [J].
Hosing, Chitra ;
Saliba, Rima M. ;
Hamerschlak, Nelson ;
Kutner, Jose Mauro ;
Sakashita, Araci Massami ;
Kondo, Andrea Tiemi ;
Rodrigues, Morgani ;
Fernande, Juliana Folloni ;
Chiattone, Alexandre ;
Chiattone, Viviane C. ;
Barros, Jose C. ;
Chiattone, Carlos S. ;
Chiattone, Ricardo ;
Popat, Uday ;
Qazilbash, Muzaffar ;
Tang, Xiao Wen ;
Wu, Depei ;
Majilis, Alejandro ;
de Lima, Marcos ;
Anguita, Timoleon .
TRANSFUSION, 2014, 54 (04) :1081-1087
[9]   A cell-kinetic model of CD34+cell mobilization and harvest:: development of a predictive algorithm for CD34+cell yield in PBPC collections [J].
Humpe, A ;
Riggert, J ;
Meineke, I ;
Kurz, M ;
Eil, A ;
Storkebaum, B ;
Binder, C ;
Munzel, U ;
Funke, I ;
Höcker, P ;
Wiesneth, M ;
Köhler, M .
TRANSFUSION, 2000, 40 (11) :1363-1370
[10]   Peripheral blood progenitor cell collection by two programs for autologous and allogeneic transplantation [J].
Ikeda, Kazuhiko ;
Ohto, Hitoshi ;
Kanno, Takahiro ;
Gonda, Kenji ;
Suzuki, Yuhko ;
Ono, Takako ;
Saito, Shunnichi ;
Takahashi, Hiroshi ;
Kimura, Satoshi ;
Harada-Shirado, Kayo ;
Yamauchi, Hiroyuki ;
Hoshino, Yasuto ;
Mashimo, Yumiko ;
Nollet, Kenneth E. ;
Kikuta, Atsushi ;
Ogawa, Kazuei ;
Takeishi, Yasuchika .
TRANSFUSION, 2014, 54 (05) :1235-1242