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在318例II - III期乳腺癌患者中,两种剂量环磷酰胺联合依托泊苷及粒细胞集落刺激因子用于动员外周血干细胞的随机试验。

A randomized trial of two doses of cyclophosphamide with etoposide and G-CSF for mobilization of peripheral blood stem cells in 318 patients with stage II-III breast cancer.

作者信息

Schwartzberg L S, Weaver C H, Birch R, Manner C, Tauer K, Beeker T, Morgan-Ihrig C, MacAneny B, Leff R, Smith R, Hainsworth J, Greco T, Schwerkoske J, Murphy M N, Buckner C D

机构信息

Clinical Trials Division of Response Oncology, Inc., Memphis, TN 38117, USA.

出版信息

J Hematother. 1998 Apr;7(2):141-50. doi: 10.1089/scd.1.1998.7.141.

Abstract

The purpose of this study was to develop a less toxic outpatient chemotherapy regimen for mobilizing peripheral blood stem cells (PBSC). Three hundred eighteen patients with newly diagnosed stage II-III breast cancer who had received conventional dose adjuvant chemotherapy were randomized to receive intermediate-dose cyclophosphamide (2 g/m2), etoposide (600 mg/m2), and granulocyte colony-stimulating factor (G-CSF) 6 micrograms/kg/day (ID-Cy, n = 162) or high-dose cyclophosphamide (4 g/m2) and the same doses of etoposide and G-CSF (HD-Cy, n = 156) followed by collection of PBSC. Three hundred seventeen of 318 patients had apheresis performed, and 315 received high-dose chemotherapy (HDC) followed by PBSC support. The median numbers of CD34+ cells collected in a median of two apheresis following ID-Cy and HD-Cy were 19.9 and 22.2 x 10(6)/kg, respectively (p = 0.04). The fractions of patients achieving CD34+ cell doses > or = 2.5 or > or = 5.0 x 10(6)/kg were not different between the two regimens. More patients receiving HD-Cy had grade 3-4 nausea (p = 0.001), vomiting (p = 0.03), and mucositis (p = 0.04). The fractions of patients having a neutrophil nadir < 0.5 x 10(9)/L following ID-Cy and HD-Cy were 0.83 and 0.95, respectively (p = < 0.001). The fractions of patients having a platelet nadir < 25 x 10(9)/L following ID-Cy and HD-Cy were 0.13 and 0.51, respectively (p = < 0.001). More patients in the HD-Cy group received platelet (p < 0.001) and red blood cell (p < 0.001) transfusions and were admitted to the hospital more frequently (p = 0.03) than patients receiving ID-Cy. Three hundred fifteen patients received HDC followed by infusion of PBSC. There were no significant differences in the incidence of transplant-related death or early survival between patients receiving ID-Cy or HD-Cy followed by HDC. It was concluded that a regimen of Cy 2 g/m2 with etoposide and G-CSF was effective for mobilization of PBSC with low morbidity and resource utilization in patients with limited prior chemotherapy exposure.

摘要

本研究的目的是开发一种毒性较小的门诊化疗方案,用于动员外周血干细胞(PBSC)。318例新诊断的II-III期乳腺癌患者接受了常规剂量辅助化疗,被随机分为两组,一组接受中等剂量环磷酰胺(2 g/m2)、依托泊苷(600 mg/m2)和粒细胞集落刺激因子(G-CSF)6微克/千克/天(ID-Cy组,n = 162),另一组接受高剂量环磷酰胺(4 g/m2)以及相同剂量的依托泊苷和G-CSF(HD-Cy组,n = 156),随后采集PBSC。318例患者中有317例进行了单采,315例接受了大剂量化疗(HDC)并接受PBSC支持。ID-Cy组和HD-Cy组在中位两次单采后采集的CD34+细胞中位数分别为19.9和22.2×10(6)/kg(p = 0.04)。两组方案中达到CD34+细胞剂量≥2.5或≥5.0×10(6)/kg的患者比例无差异。接受HD-Cy组的更多患者出现3-4级恶心(p = 0.001)、呕吐(p = 0.03)和粘膜炎(p = 0.04)。ID-Cy组和HD-Cy组中性粒细胞最低点<0.5×10(9)/L的患者比例分别为0.83和0.95(p = <0.001)。ID-Cy组和HD-Cy组血小板最低点<25×10(9)/L的患者比例分别为0.13和0.51(p = <0.001)。与接受ID-Cy组的患者相比,HD-Cy组更多患者接受了血小板(p <0.001)和红细胞(p <0.001)输注,且住院频率更高(p = 0.03)。315例患者接受了HDC并随后输注PBSC。接受ID-Cy或HD-Cy后再进行HDC的患者,移植相关死亡或早期生存率无显著差异。研究得出结论,对于既往化疗暴露有限的患者,Cy 2 g/m2联合依托泊苷和G-CSF的方案在动员PBSC方面有效,且发病率和资源利用率较低。

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