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The effective use of plerixafor as a real‐time rescue strategy for patients poorly mobilizing autologous CD34 + cells
Author(s) -
Gopal Ajay K.,
Karami Mehdi,
Mayor JoAl,
Macebeo Mylene,
Linenberger Michael,
Bensinger William I.,
Holmberg Leona
Publication year - 2012
Publication title -
journal of clinical apheresis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.697
H-Index - 46
eISSN - 1098-1101
pISSN - 0733-2459
DOI - 10.1002/jca.21206
Subject(s) - plerixafor , medicine , apheresis , cd34 , multiple myeloma , mobilization , surgery , urology , stem cell , cxcr4 , biology , history , platelet , chemokine , receptor , archaeology , genetics
Abstract Plerixafor enhances CD34 + cell mobilization, however, its optimal use is unknown. We hypothesized that plerixafor could “rescue” patients in the midst of mobilization when factors indicated a poor CD34 + yield. Of 295 consecutive autologous peripheral blood mobilization attempts at our center, 39 (13%) used plerixafor as rescue strategy due to a CD34 + cell concentration <10/μl (median 5.95/μl, n = 30), low CD34 + cell yield from prior apheresis day (median 1.06 × 10 6 CD34 + cells/kg, n = 7), or other ( n = 2). Patients received a median of one plerixafor dose (range: 1–4). Thirty‐four (87%) collected =2 × 10 6 CD34 + cells/kg and 26 (67%) collected =4 × 10 6 CD34 + cells/kg. Median collections for lymphoma ( n = 24) and myeloma ( n = 15) patients were 4.1 × 10 6 and 8.3 × 10 6 CD34/kg, respectively. A single dose of plerixafor was associated with an increase in the mean peripheral blood CD34 + concentration of 17.2 cells/μl ( P < 0.001) and mean increased CD34 + cell yield following a single apheresis of 5.11 × 10 6 /kg ( P < 0.03). A real‐time rescue use of plerixafor is feasible and may allow targeted use of this agent. J. Clin. Apheresis, 2012. © 2012 Wiley Periodicals, Inc.