普乐沙福
医学
粒细胞集落刺激因子
环磷酰胺
化疗
阿糖胞苷
动员
内科学
多发性骨髓瘤
肿瘤科
胃肠病学
外科
受体
考古
历史
趋化因子
CXCR4型
作者
Giuseppe Milone,Massimo Martino,Andrea Spadaro,Salvatore Leotta,Annalia Di Marco,Potito Rosario Scalzulli,Alessandra Cupri,Valentina Martina,Elena Schinocca,Eleonora Spina,Giovanni Tripepi
摘要
Summary To date, no prospective study on P lerixafor ‘on‐demand’ in combination with chemotherapy and granulocyte colony‐stimulating factor ( G ‐ CSF ) has been reported. We present an interim analysis of the first prospective study in which Plerixafor was administered on‐demand in patients affected by multiple myeloma and lymphoma who received high dose cyclophosphamide or DHAP (dexamethasone, cytarabine, cisplatin) plus G ‐ CSF to mobilize peripheral blood stem cells ( PBSC ). One hundred and two patients were evaluable for response. A cohort of 240 patients receiving the same mobilizing chemotherapy was retrospectively studied. Failure to mobilize CD 34 + cells in peripheral blood was reduced by ‘on‐demand’ strategy compared to conventional mobilization; from 13·0 to 3·0% ( P = 0·004). Failure to harvest CD 34 + cells 2 × 10 6 /kg decreased from 20·9 to 4·0% ( P = 0·0001). The on‐demand P lerixafor strategy also resulted in a lower rate of mobilization failure ( P = 0·03) and harvest failure ( P = 0·0008) when compared to a ‘bias‐adjusted set of controls’. Evaluation of economic costs of the two strategies showed that the overall cost of the two treatments were comparable when salvage mobilizations were taken into account. When in combination with cyclophosphamide or DHAP plus G ‐ CSF , the ‘on‐demand’ use of P lerixafor showed, in comparison to conventionally treated patients, a significant improvement in mobilization of PBSC with no increase in overall cost.
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