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Efficacy of vinorelbine, epirubicin and prednisone combination regimen in pretreated elderly patients with aggressive non-Hodgkin's lymphoma | Haematologica

机译:长春瑞滨,表柔比星和强的松联合方案对老年老年侵袭性非霍奇金淋巴瘤患者的疗效血液学

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BACKGROUND AND OBJECTIVES: To assess the efficacy and toxic profile of the NAEPP protocol, a regimen including vinorelbine, epirubicin and prednisone, in a particularly troublesome subset of patients: pretreated elderly patients with aggressive non-Hodgkin's lymphoma (NHL). DESIGN AND METHODS: From November 1998 to January 2000, 20 pretreated patients who had all relapsed after first-line VNCOP-B chemotherapy were enrolled in a phase II trial and treated with the NAEPP regimen: vinorelbine (25 mg/m(2) i.v. on days 1 and 8), epirubicin (40 mg/m(2) i.v. on days 1 and 8), and prednisone (40 mg/m(2) on days 1 and 8) with granulocyte colony-stimulating factor administered at 5 mg/kg/day on days 2-5 and days 9-12. Chemotherapy was repeated every 4 weeks for a total of 6 cycles. RESULTS: Six (30%) patients achieved complete remission (CR) and 7 (35%) had partial responses (PR), giving an overall response rate of 65%. The response rate was not affected either by type of relapse presentation (nodal versus nodal plus extranodal), presence of bulky disease, or time of relapse. No major toxic effects were recorded. INTERPRETATION AND CONCLUSIONS: These preliminary data suggest that the NAEPP regimen is an effective combination with a low toxicity profile in elderly pretreated patients with aggressive NHL. Further trials using NAEPP as a consolidation phase following first-line treatment are needed to establish the advantage in terms of CR rate and relapse-free survival in these patients.
机译:背景与目的:为了评估NAEPP方案的疗效和毒性,该方案包括长春瑞滨,表柔比星和强的松,适用于特别麻烦的患者亚组:患有侵袭性非霍奇金淋巴瘤(NHL)的老年患者。设计与方法:从1998年11月至2000年1月,对20例在一线VNCOP-B化疗后全部复发的预治疗患者进行了II期试验,并接受了NAEPP方案长春瑞滨(25 mg / m(2)iv第1天和第8天),表柔比星(第1天和第8天静脉注射40 mg / m(2))和泼尼松(第1天和第8天40 mg / m(2))和粒细胞集落刺激因子5 mg / kg / day在第2-5天和第9-12天。每4周重复一次化学疗法,共6个周期。结果:六名(30%)患者获得了完全缓解(CR),七名(35%)出现了部分缓解(PR),总体缓解率为65%。缓解率不受复发表现类型(淋巴结对淋巴结加结外),是否存在大块疾病或复发时间的影响。没有发现主要的毒性作用。解释和结论:这些初步数据表明,NAEPP方案在老年积极的NHL预处理患者中是一种有效的组合,且毒性低。一线治疗后需要使用NAEPP作为巩固期的进一步试验,以建立这些患者在CR率和无复发生存方面的优势。

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