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首页> 外文期刊>Clinical lymphoma, myeloma & leukemia >High-dose Thiotepa, Busulfan, Cyclophosphamide, and Autologous Stem Cell Transplantation as Upfront Consolidation for Systemic Non-Hodgkin Lymphoma With Synchronous Central Nervous System Involvement
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High-dose Thiotepa, Busulfan, Cyclophosphamide, and Autologous Stem Cell Transplantation as Upfront Consolidation for Systemic Non-Hodgkin Lymphoma With Synchronous Central Nervous System Involvement

机译:高剂量Thiotepa,Busulfan,环磷酰胺和自体干细胞移植作为全身非霍奇金淋巴瘤的前期固结,同步中枢神经系统受累

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摘要

Micro-Abstract Systemic non-Hodgkin lymphoma with synchronous central nervous system involvement traditionally carries a poor prognosis. We found encouraging results with the use of high-dose chemotherapy and autologous stem cell transplantation as consolidation for patients in first complete remission. Central nervous system-directed conditioning with a thiotepa-based regimen might reduce the incidence of relapse and improve the outcomes in this population. Abstract Introduction Synchronous involvement of the central nervous system (CNS) at the diagnosis of systemic non-Hodgkin lymphoma (NHL) is associated with an increased risk for relapse despite complete remission to initial therapy. High-dose chemotherapy with a CNS-directed conditioning regimen followed by autologous stem cell transplantation (ASCT) holds promise as a consolidative approach. Patients and Methods We conducted a retrospective analysis of all patients with systemic B-cell NHL and synchronous CNS involvement who received upfront consolidation with high-dose chemotherapy with thiotepa, busulfan, cyclophosphamide, and ASCT while in first complete remission between July 2008 and June 2016 at 2 partner academic institutions. Results Twenty patients were identified through the transplant database. The median age at diagnosis was 53 years (range, 37-65 years). The majority had diffuse large B-cell lymphoma histology (n?= 17; 85%). The sites of CNS involvement were parenchymal (n?= 12; 60%) and leptomeningeal disease (n?= 9; 45%). All patients received systemic and CNS-directed therapy prior to transplant, with the most common approaches being R-CHOP (rituximab, cyclophosphamide, vincristine, doxorubicin, and prednisolone) (n?= 13; 65%) and high-dose intravenous methotrexate (n?= 16; 80%), respectively. With a median follow up of 4.4 years after ASCT (range, 2 months-8.5 years), the Kaplan-Meier estimates of 4-year progression-free and overall survival were 77% (95% confidence interval, 48%-91%) and 82% (95% confidence interval, 54%-94%), respectively. Conclusion CNS-directed high-dose chemotherapy and ASCT provides durable remission for patients with synchronous aggressive lymphoma and should be strongly considered as consolidative therapy for eligible patients with systemic NHL with CNS involvement in first complete remission.
机译:具有同步中枢神经系统的微摘要系统性非霍奇金淋巴瘤传统上具有较差的预后。我们发现使用高剂量化疗和自体干细胞移植的令人鼓舞的结果作为患者在首次完全缓解中的固结。中枢神经系统定向调节Thiotepa的方案可能会降低复发的发生率,并改善该人群的结果。摘要中枢神经系统(CNS)在系统性非霍奇金淋巴瘤(NHL)诊断时的同步参与与初始治疗完全缓解的复发风险增加有关。具有CNS定向调理方案的高剂量化疗,然后是自体干细胞移植(ASCT)作为一种巩固方法,承担承担的承担。患者和方法我们对所有系统性B细胞NHL和同步CNS参与进行了回顾性分析,以及通过Thiotepa,Busulfan,环磷酰胺和ASCT的高剂量化疗接受前期固结,同时在2008年7月至2016年6月至6月期间进行了第一次完全缓解在2个合作伙伴学术机构。结果通过移植数据库鉴定出二十名患者。诊断的中位年龄为53岁(范围,37-65岁)。大多数弥漫性大B细胞淋巴瘤组织学(n?= 17; 85%)。 CNS参与的位点是实质的(n?= 12; 60%)和百分症疾病(n?= 9; 45%)。所有患者在移植之前接受全身和CNS定向治疗,具有最常见的方法是R-Chec(Rituximab,环磷酰胺,血管内,多柔比星和泼尼松酮)(n?= 13; 65%)和高剂量静脉内甲氨蝶呤( n?= 16; 80%)。在ASCT(范围为2个月 - 8.5年)后,中位于4.4岁以下,Kaplan-Meier估计为4年的无进展和整体生存率为77%(95%置信区间,48%-91%)分别为82%(95%置信区间,54%-94%)。结论CNS针对高剂量化疗和ASCT为同步侵袭性淋巴瘤的患者提供耐用的缓解,并且应被强烈被视为符合CNS患者的合格疗法,CNS参与首次完全缓解。

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