首页> 外文OA文献 >Bendamustine in Combination With Gemcitabine and Vinorelbine Is an Effective Regimen As Induction Chemotherapy Before Autologous Stem-Cell Transplantation for Relapsed or Refractory Hodgkin Lymphoma: Final Results of a Multicenter Phase II Study
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Bendamustine in Combination With Gemcitabine and Vinorelbine Is an Effective Regimen As Induction Chemotherapy Before Autologous Stem-Cell Transplantation for Relapsed or Refractory Hodgkin Lymphoma: Final Results of a Multicenter Phase II Study

机译:Bendamustine与Gemcitabine和Vinorelbine的组合是一种有效的方案,作为在复发或难治性霍奇金淋巴瘤复发或难治性霍奇金淋巴瘤的自体干细胞移植之前:多中心期II研究的最终结果

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摘要

Purpose: This multicenter, open-label, phase II study evaluated the combination of bendamustine, gemcitabine, and vinorelbine (BeGEV) as induction therapy before autologous stem-cell transplantation (ASCT) in patients with relapsed or refractory Hodgkin lymphoma (HL). Patients and Methods: Patients with HL who were refractory to or had relapsed after one previous chemotherapy line were eligible. The primary end point was complete response (CR) rate after four cycles of therapy. Secondary end points were: overall response rate, stem-cell mobilization activity, and toxicity. Progression-free and overall survival were also evaluated. Results: In total, 59 patients were enrolled. After four cycles of therapy, 43 patients (73%) achieved CR, and six (10%) achieved partial response, for an overall response rate of 83%. The most common grade 3 to 4 nonhematologic toxicities included febrile neutropenia (n = 7) and infection (n = 4). Regarding hematologic toxicities, grade 3 to 4 thrombocytopenia and neutropenia were each experienced by eight patients (13.5%). CD34+ cells were successfully harvested in 55 of 57 evaluable patients, and 43 of 49 responding patients underwent ASCT. With a median follow-up of 29 months, the 2-year progression-free and overall survival rates for the total population were 62.2% and 77.6%, respectively. The same figures for patients undergoing autograft were 80.8% and 89.3%, respectively. Conclusion: This phase II study demonstrates that BeGEV is an effective salvage regimen able to induce CR in a high proportion of patients with relapsed or refractory HL before ASCT. These data provide a strong rationale for further development of the BeGEV regimen.
机译:目的:该多中心,开放标签,II期研究评估了Bendamustine,Gemcitabine和Vinorelbine(Begev)的组合作为复发或难治性霍奇金淋巴瘤(HL)患者的自体干细胞移植(ASCT)之前的感应治疗。患者和方法:HL患者在先前的化疗线后难以或已复发。在四个循环治疗后,主要终点是完全响应(CR)速率。次要终点是:总体反应率,干细胞动员活性,毒性。还评估了无进展和整体存活。结果:总共有59名患者注册。经过四个循环的治疗后,43名患者(73%)实现CR,六(10%)实现部分反应,总响应率为83%。最常见的3至4级非活血管学毒性包括发热中性粒细胞减少(n = 7)和感染(n = 4)。关于血液学毒性,八级患者每次经历3至4级血管发育症和中性粒细胞病症(13.5%)。在57例可评估患者中成功收获CD34 +细胞,43例患有43名响应患者ASCT。凭借29个月的中位随访,总人口的2年无进展和整体生存率分别为62.2%和77.6%。接受自体移植的患者的相同图分别为80.8%和89.3%。结论:本II期研究表明,Begev是一种有效的挽救方案,能够在高比例的患者中诱导CR的患者ASCT之前的复发或难治性HL。这些数据提供了强烈的基本理由,以进一步发展Begev方案。

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