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Blood, 15 August 2008, Vol. 112, No. 4, pp. 990-998.
Prepublished online as a Blood First Edition Paper on April 21, 2008; DOI 10.1182/blood-2007-12-130179.
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Submitted December 19, 2007
Accepted April 7, 2008
Rapid mobilization of functional donor hematopoietic cells without G-CSF using plerixafor, an antagonist of the CXCR4/SDF-1 interaction
Steven M Devine*, Ravi Vij, Michael Rettig, Laura Todt, Kiley McGlauchlen, Nicholas Fisher, Hollie Devine, Daniel C Link, Gary Calandra, Gary Bridger, Peter Westervelt, and John F DiPersio
Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio, United States
Medicine, Washington University, St Louis, Missouri, United States
Genzyme Inc, Genzyme Inc, Cambridge, MA, United States
* Corresponding author; email: steven.devine{at}osumc.edu.
Allografts from HLA-matched sibling donors were mobilized and collected without G-CSF using Plerixafor (AMD3100), a direct antagonist of CXCR4/SDF-1. Donors (N=25) were treated with AMD3100 at a dose of 240 µg/kg by subcutaneous injection and leukapheresis was then initiated just 4 hours later. Two-thirds of the donors collected an allograft with a CD34+ cell dose sufficient for transplantation after just one dose of AMD3100. No donor experienced more than grade one toxicity. Following a myeloablative regimen, twenty patients with hematological malignancies received allografts collected after AMD3100 alone. All patients engrafted neutrophils (median day +10) and platelets (median day +12) promptly. Acute GVHD grades 2-4 occurred in 35% of patients. One patient died due to complications related to acute GVHD. No unexpected adverse events were observed in any of the recipients. All 14 patients surviving in remission have robust trilineage hematopoiesis and are transfusion-free with a median follow-up of 277 days (range 139-964 days). Direct antagonism of CXCR4 by AMD3100 may provide a more rapid and possibly less toxic and cumbersome alternative to traditional G-CSF-based mobilization in normal donors. This trial was registered as #NCT00241358 at www.ClinicalTrials.gov

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