首页> 美国卫生研究院文献>Journal of Clinical and Experimental Hematopathology : JCEH >Dose-Modified Ifosfamide Epirubicin and Etoposide is a Safe and EffectiveSalvage Therapy with High Peripheral Blood Stem Cell Mobilization Capacity for PoorlyMobilized Hodgkin’s Lymphoma and Non-Hodgkin’s Lymphoma Patients
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Dose-Modified Ifosfamide Epirubicin and Etoposide is a Safe and EffectiveSalvage Therapy with High Peripheral Blood Stem Cell Mobilization Capacity for PoorlyMobilized Hodgkin’s Lymphoma and Non-Hodgkin’s Lymphoma Patients

机译:剂量修饰的异环磷酰胺表柔比星和依托泊苷是安全有效的高外周血干细胞动员能力的抢救疗法动员霍奇金淋巴瘤和非霍奇金淋巴瘤患者

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摘要

A dose modified ifosfamide, epirubicin, and etoposide (IVE) regimen was prospectively assessed for its efficacy in mobilizing peripheral blood stem cells for autologous transplantation. Two patients with Hodgkin’s lymphoma and two with non-Hodgkin’s lymphoma who were undergoing stem cell therapy were studied. All patients had a history of multiple treatments with insufficient stem cell mobilization. The dose modified IVE regimen consisted of ifosfamide 3 g/m2 intravenously (IV) administered on days 1-2 in combination with epirubicin 50 mg/m2 IV on day 1 and etoposide 200 mg/m2 (100 mg/m2 in two patients with complete remission) IV on days 1-3. The ifosfamide dosage was reduced to two-thirds of the original protocol. A substantial high yield of CD34+ cells was achieved when patients were treated with a dose-modified IVE regimen, compared with that during the previous regimen (two with the ifosfamide, carboplatin, and etoposide [ICE] regimen, one with high-dose cyclophosphamide and one with the original IVE regimen). Two patients who had refractory and residual disease received a 200 mg/m2 dose of etoposide, which resulted in tumor reduction (one patient with complete remission and one with further reduction in tumor size). After the IVE regimen, all four patients had a sufficient yield of CD34+ cells in total, which was available for stem cell transplantation.Hematological and non-hematological toxicities were comparable in all regimens. Thissingle-center prospective study demonstrated that the dose-modified IVE regimen can beused as a safe treatment with high mobilizing efficacy in heavily pretreated lymphomapatients.
机译:前瞻性评估了剂量改良的异环磷酰胺,表柔比星和依托泊苷(IVE)方案在动员外周血干细胞进行自体移植中的功效。研究了两名正在接受干细胞治疗的霍奇金淋巴瘤患者和两名非霍奇金淋巴瘤患者。所有患者都有干细胞动员不足的多次治疗史。改良剂量的IVE方案包括在第1-2天静脉注射(iv)异环磷酰胺3 g / m 2 与在第1天联合表柔比星50 mg / m 2 和依托泊苷200 mg / m 2 (两名完全缓解的患者100 mg / m 2 )在第1-3天静脉注射。异环磷酰胺的剂量减少到原始方案的三分之二。与之前的方案相比(两次使用异环磷酰胺,卡铂和依托泊苷[ICE]方案),采用剂量修改的IVE方案治疗的患者获得了很高的CD34 + 细胞产量。 ,一种使用大剂量环磷酰胺,另一种使用原始IVE方案)。两名患有顽固性和残留性疾病的患者接受了200 mg / m 2 剂量的依托泊苷,导致肿瘤缩小(一名患者完全缓解,另一名患者肿瘤大小进一步缩小)。 IVE方案后,所有四名患者的CD34 + 细胞总数均足够高,可用于干细胞移植。在所有方案中血液学和非血液学毒性均相当。这个单中心前瞻性研究表明,剂量调整的IVE方案可以在高度预处理的淋巴瘤中用作安全治疗方法,具有高动员功效耐心。

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