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大剂量化疗联合自体造血干细胞支持治疗复发或难治性原发性中枢神经系统淋巴瘤:德国合作 PCNSL 研究组的前瞻性多中心试验。

High-dose chemotherapy with autologous haematopoietic stem cell support for relapsed or refractory primary CNS lymphoma: a prospective multicentre trial by the German Cooperative PCNSL study group.

机构信息

Department of Haematology/Oncology, Klinikum Stuttgart, Stuttgart, Germany.

Department of Medical Oncology & Institute for Clinical Epidemiology and Biostatistics, University Hospital Basel, Basel, Switzerland.

出版信息

Leukemia. 2017 Dec;31(12):2623-2629. doi: 10.1038/leu.2017.170. Epub 2017 May 31.

Abstract

To investigate safety and efficacy of high-dose chemotherapy followed by autologous stem cell transplantation (HCT-ASCT) in relapsed/refractory (r/r) primary central nervous system lymphoma (PCNSL), we conducted a single-arm multicentre study for immunocompetent patients (<66 years) with PCNSL failing high-dose methotrexate)-based chemotherapy. Induction consisted of two courses of rituximab (375 mg/m), high-dose cytarabine (2 × 3 g/m) and thiotepa (40 mg/m) with collection of stem cells in between. Conditioning for HCT-ASCT consisted of rituximab 375 mg/m, carmustine 400 mg/m and thiotepa (4 × 5 mg/kg). Patients commenced HCT-ASCT irrespective of response after induction. Patients not achieving complete remission (CR) after HCT-ASCT received whole-brain radiotherapy. Primary end point was CR after HCT-ASCT. We enrolled 39 patients; median age and Karnofsky performance score are 57 years and 90%, respectively. About 28 patients had relapsed and 8 refractory disease. About 22 patients responded to induction and 32 patients commenced HCT-ASCT. About 22 patients (56.4%) achieved CR after HCT-ASCT. Respective 2-year progression-free survival (PFS) and overall survival (OS) rates were 46.0% (median PFS 12.4 months) and 56.4%; median OS not reached. We recorded four treatment-related deaths. Thiotepa-based HCT-ASCT is an effective treatment option in eligible patients with r/r PCNSL. Comparative studies are needed to further scrutinise the role of HCT-ASCT in the salvage setting.

摘要

为了研究大剂量化疗(HCT-ASCT)后继自体干细胞移植(ASCT)在复发/难治性(r/r)原发性中枢神经系统淋巴瘤(PCNSL)中的安全性和疗效,我们对免疫功能正常(<66 岁)、接受大剂量甲氨蝶呤(HDMTX)为基础的化疗后复发/难治的 PCNSL 患者进行了一项单臂多中心研究。诱导治疗包括两个疗程的利妥昔单抗(375mg/m2)、高剂量阿糖胞苷(2×3g/m2)和噻替哌(40mg/m2),中间采集干细胞。HCT-ASCT 的预处理方案包括利妥昔单抗 375mg/m2、卡莫司汀 400mg/m2 和噻替哌(4×5mg/kg)。患者在诱导治疗后无论反应如何都开始进行 HCT-ASCT。HCT-ASCT 后未达到完全缓解(CR)的患者接受全脑放疗。主要终点是 HCT-ASCT 后的 CR。我们共纳入 39 例患者;中位年龄和 Karnofsky 表现评分分别为 57 岁和 90%。约 28 例患者复发,8 例患者难治。约 22 例患者对诱导治疗有反应,32 例患者开始进行 HCT-ASCT。约 22 例(56.4%)患者在 HCT-ASCT 后达到 CR。相应的 2 年无进展生存率(PFS)和总生存率(OS)分别为 46.0%(中位 PFS 为 12.4 个月)和 56.4%;中位 OS 未达到。我们记录了 4 例与治疗相关的死亡。以噻替哌为基础的 HCT-ASCT 是 r/r PCNSL 患者的有效治疗选择。需要进行比较研究,以进一步探讨 HCT-ASCT 在挽救治疗中的作用。

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