%0 Journal Article
%T Plerixafor for autologous CD34+ cell mobilization
%A Huda Salman
%A Hillard M Lazarus
%J Core Evidence
%D 2011
%I 
%R http://dx.doi.org/10.2147/CE.S7801
%X ixafor for autologous CD34+ cell mobilization Review (3887) Total Article Views Authors: Huda Salman, Hillard M Lazarus Published Date February 2011 Volume 2011:6 Pages 23 - 29 DOI: http://dx.doi.org/10.2147/CE.S7801 Huda Salman, Hillard M Lazarus Division of Hematology-Oncology, Blood and Marrow Transplant Program, University Hospitals Case Medical Center, Case Comprehensive Cancer Center, Case Western Reserve University School of Medicine, Cleveland, OH, USA Abstract: High-dose chemotherapy and autologous transplantation of hematopoietic cells is a crucial treatment option for hematologic malignancy patients. Current mobilization regimes often do not provide adequate numbers of CD34+ cells. The chemokine receptor CXCR4 and ligand SDF-1 are integrally involved in homing and mobilization of hematopoietic progenitor cells. Disruption of the CXCR4/SDF-1 axis by the CXCR4 antagonist, plerixafor, has been demonstrated in Phase II and Phase III trials to improve mobilization when used in conjunction with granulocyte colony-stimulating factor (G-CSF). This approach is safe with few adverse events and produces significantly greater numbers of CD34+ cells when compared to G-CSF alone. New plerixafor initiatives include use in volunteer donors for allogeneic hematopoietic cell transplant and in other disease targets.
%K plerixafor
%K autologous hematopoietic cell transplant
%K CD34
%K lymphoma
%K myeloma
%K granulocyte colony-stimulating factor (G-CSF)
%U https://www.dovepress.com/plerixafor-for-autologous-cd34-cell-mobilization-peer-reviewed-article-CE