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首页> 外文期刊>Leukemia and lymphoma >Treatment of high-risk aggressive B-cell non-Hodgkin lymphomas with rituximab, intensive induction and high-dose consolidation: long-term analysis of the R-MegaCHOP-ESHAP-BEAM Trial
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Treatment of high-risk aggressive B-cell non-Hodgkin lymphomas with rituximab, intensive induction and high-dose consolidation: long-term analysis of the R-MegaCHOP-ESHAP-BEAM Trial

机译:利妥昔单抗,密集诱导和大剂量合并治疗高危侵袭性B细胞非霍奇金淋巴瘤:R-MegaCHOP-ESHAP-BEAM试验的长期分析

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摘要

We have studied the feasibility and efficacy of intensifi ed R-MegaCHOP-ESHAP-BEAM therapy in high-risk aggressive B-cell lymphomas. Altogether 105 patients (19 -64 years) with diff use large B-cell lymphoma (DLBCL), primary mediastinal B-cell lymphoma (PMBL) or follicular lymphoma grade 3 (FL3) with an age-adjusted International Prognostic Index of 2 -3 were recruited. Treatment consisted of three cycles of high-dose R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine, prednisone), followed by three cycles of R-ESHAP (rituximab, etoposide, methylprednisolone, cytarabine, cisplatin) and highdose consolidation with BEAM (BCNU, etoposide, cytarabine, melphalan) and autologous stem cell transplant. The 5-year progression-free survival (PFS) was 72% (DLBCL 60%, PMBL 89%) and overall survival (OS) was 74% (DLBCL 61%, PMBL 89%) after a median follow-up of 85 months. However, an independent prognostic factor was age only, with patients <= 45 years having 5-year PFS 90% and patients > 45 years having PFS 54%. PMBL had better prognosis than DLBCL/FL3 in patients > 45 years (PFS, 88% vs. 48%), but not in younger patients (PFS, 91% vs. 94%).
机译:我们已经研究了强化R-MegaCHOP-ESHAP-BEAM治疗高危侵袭性B细胞淋巴瘤的可行性和有效性。共有105例(19 -64岁)diff患者使用年龄调整后的国际预后指数为2 -3的大B细胞淋巴瘤(DLBCL),原发性纵隔B细胞淋巴瘤(PMBL)或3级滤泡性淋巴瘤(FL3)。被招募。治疗包括三个周期的大剂量R-CHOP(利妥昔单抗,环磷酰胺,阿霉素,长春新碱,泼尼松),然后三个周期的R-ESHAP(利妥昔单抗,依托泊苷,甲基强的松龙,阿糖胞苷,顺铂)和大剂量巩固与BEAM(BCNU) ,依托泊苷,阿糖胞苷,美法仑)和自体干细胞移植。中位随访85个月后的5年无进展生存期(PFS)为72%(DLBCL 60%,PMBL 89%),总生存期(OS)为74%(DLBCL 61%,PMBL 89%) 。但是,独立的预后因素仅是年龄,<= 45岁的患者5年PFS为90%,> 45岁的患者为PFS 54%。在> 45岁的患者中,PMBL的预后比DLBCL / FL3好(PFS,88%对48%),但在年轻患者中则不然(PFS,91%对94%)。

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