| Literature DB >> 28631842 |
Kenneth W Douglas1, Maria Gilleece2, Patrick Hayden3, Hannah Hunter4, Peter R E Johnson5, Charlotte Kallmeyer6, Ram K Malladi7, Shankara Paneesha8, Rachel Pawson9, Michael Quinn10, Kavita Raj11, Deborah Richardson12, Stephen Robinson13, Nigel Russell14, John Snowden15, Anna Sureda16, Eleni Tholouli17, Kirsty Thomson18, Mike Watts19, Keith M Wilson20.
Abstract
Plerixafor is a CXC chemokine receptor (CXCR4) antagonist that mobilizes stem cells in the peripheral blood. It is indicated (in combination with granulocyte-colony stimulating factor [G-CSF]) to enhance the harvest of adequate quantities of cluster differentiation (CD) 34+ cells for autologous transplantation in patients with lymphoma or multiple myeloma whose cells mobilize poorly. Strategies for use include delayed re-mobilization after a failed mobilization attempt with G-CSF, and rescue or pre-emptive mobilization in patients in whom mobilization with G-CSF is likely to fail. Pre-emptive use has the advantage that it avoids the need to re-schedule the transplant procedure, with its attendant inconvenience, quality-of-life issues for the patient and cost of additional admissions to the transplant unit. UK experience from 2 major centers suggests that pre-emptive plerixafor is associated with an incremental drug cost of less than £2000 when averaged over all patients undergoing peripheral blood stem cell (PBSC) transplant. A CD34+ cell count of <15 µl-1 at the time of recovery after chemomobilization or after four days of G-CSF treatment, or an apheresis yield of <1 × 106 CD34+ cells/kg on the first day of apheresis, could be used to predict the need for pre-emptive plerixafor.Entities:
Keywords: Peripheral blood stem cell mobilization; autologous PBSC transplant; consensus statement; mobilization failure; plerixafor
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Year: 2017 PMID: 28631842 DOI: 10.1002/jca.21563
Source DB: PubMed Journal: J Clin Apher ISSN: 0733-2459 Impact factor: 2.821