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A new model for predicting the timing of leukapheresis on the basis of CD34+ cell and hematopoietic progenitor cell levels

✍ Scribed by Hao-Wei Teng; Liang-Tsai Hsiao; Shu-Chou Chaou; Jyh-Pyng Gau; Tzu-Chi Lee; Ying-Yih Shih; Chun-Yu Liu; Ying-Chung Hong; Ming-Huang Chen; Mu-Hsin Chang; Ya-Hsu Yang; Po-Min Chen


Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
278 KB
Volume
22
Category
Article
ISSN
0733-2459

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✦ Synopsis


Abstract

We developed a model (depending on peripheral CD34^+^ cell count and hematopoietic progenitor cell count) to determine the optimal timing of 3‐day leukapheresis in patients pretreated with chemotherapy and G‐CSF. Marrow potentials were identified on the basis of three patterns of leukapheretic yield. Pattern 1 predicted good marrow potential. The positive predictive value of a first‐day leukapheretic yield of >1 × 10^6^ CD34^+^ cells/kg (mean 3‐day yield = 8.18 × 10^6^ CD34^+^ cells/kg, n = 11) was 100%. Pattern 2 predicted poor marrow potential. The negative predictive value of a 3‐day leukapheretic yield of >1 × 10^6^ CD34^+^ cells/kg (3‐day yield = 0.26 × 10^6^ CD34^+^ cells/kg, n = 1) was 100%. Pattern 3 met neither of the above criteria (mean 3‐day yield = 1.37 × 10^6^ CD34^+^ cells/kg, n = 19). The marrow potential was borderline and patients could be further divided into two subgroups according to peripheral CD34^+^ cell counts when WBC reached >10,000/μl. The mean yield differed significantly between pattern 1 and 3 (P < 0.001). For patients with good marrow potential, leukapheresis should begin as soon as the WBC count is >5,000/μl. Patients with borderline marrow potential may benefit from delaying leukapheresis until the WBC level is >10,000/μl and leukapheresis extended more than 3 days. J. Clin. Apheresis 2007. © 2007 Wiley‐Liss, Inc.


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