普乐沙福
医学
单采
多发性骨髓瘤
CXCR4型
粒细胞集落刺激因子
CXCR4拮抗剂
干细胞
菲格拉斯汀
移植
外科
肿瘤科
内科学
化疗
趋化因子
受体
血小板
生物
遗传学
作者
Kenneth Douglas,Maria Gilleece,Patrick Hayden,Hannah Hunter,Peter Johnson,Charlotte Kallmeyer,Ram Malladi,Shankara Paneesha,Rachel Pawson,Michael Quinn,Kavita Raj,Deborah Richardson,Stephen Robinson,Nigel H. Russell,John A. Snowden,Anna Sureda,Eleni Tholouli,Kirsty Thomson,Mike Watts,Keith Wilson
摘要
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 × 10 6 CD34+ cells/kg on the first day of apheresis, could be used to predict the need for pre‐emptive plerixafor.
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