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采用大剂量噻替派、白消安、美法仑、利妥昔单抗预处理及自体移植改善继发性中枢神经系统淋巴瘤的治疗效果。

Improving the outcomes of secondary CNS lymphoma with high-dose thiotepa, busulfan, melphalan, rituximab conditioning and autotransplant.

作者信息

Puckrin Robert, Chua Neil, Shafey Mona, Stewart Douglas A

机构信息

University of Calgary and Tom Baker Cancer Centre, Calgary, Canada.

University of Alberta and Cross Cancer Institute, Edmonton, Canada.

出版信息

Leuk Lymphoma. 2022 Oct;63(10):2444-2452. doi: 10.1080/10428194.2022.2068005. Epub 2022 Apr 22.

Abstract

Secondary central nervous system lymphoma (SCNSL) affects approximately 5% of patients with aggressive large B-cell lymphoma (LBCL) and is associated with poor outcomes. This retrospective, multicenter study included 62 consecutive patients with SCNSL intended for transplant with high-dose methotrexate (HD-MTX)-based induction followed by high-dose thiotepa, busulfan, melphalan, rituximab (TBMR) conditioning and autologous stem cell transplantation (ASCT). Median age was 58 years (range 20-75) and 52 (84%) patients had ECOG performance status >1 at diagnosis of SCNSL. Fifty-two (84%) patients completed induction and proceeded to TBMR/ASCT. With median follow-up 5.7 years, 5-year progression-free and overall survival rates were 53% (95% CI 39-65%) and 65% (95% CI 51-76%) for all patients and 62% (95% CI 45-74%) and 73% (95% CI 57-84%) for those undergoing TBMR/ASCT, respectively. Despite a historically poor prognosis, HD-MTX-based induction followed by TBMR/ASCT has the potential to achieve long-term survival in a substantial proportion of patients with SCNSL.

摘要

继发性中枢神经系统淋巴瘤(SCNSL)影响约5%的侵袭性大B细胞淋巴瘤(LBCL)患者,且与不良预后相关。这项回顾性多中心研究纳入了62例连续的SCNSL患者,这些患者拟接受以大剂量甲氨蝶呤(HD-MTX)为基础的诱导治疗,随后进行大剂量噻替派、白消安、美法仑、利妥昔单抗(TBMR)预处理及自体干细胞移植(ASCT)。中位年龄为58岁(范围20 - 75岁),52例(84%)患者在SCNSL诊断时ECOG体能状态>1。52例(84%)患者完成诱导治疗并进行了TBMR/ASCT。中位随访5.7年,所有患者的5年无进展生存率和总生存率分别为53%(95%置信区间39 - 65%)和65%(95%置信区间51 - 76%),接受TBMR/ASCT的患者分别为62%(95%置信区间45 - 74%)和73%(95%置信区间57 - 84%)。尽管历史上预后较差,但以HD-MTX为基础的诱导治疗后进行TBMR/ASCT有可能使相当一部分SCNSL患者获得长期生存。

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