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大剂量甲氨蝶呤联合替莫唑胺治疗未经治疗的原发性中枢神经系统淋巴瘤:来自中国的回顾性研究。

High-dose Methotrexate plus temozolomide with or without rituximab in patients with untreated primary central nervous system lymphoma: A retrospective study from China.

机构信息

Department of Medical Oncology, Sun Yat-Sen University Cancer Center, Guangzhou, China.

State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangzhou, China.

出版信息

Cancer Med. 2019 Apr;8(4):1359-1367. doi: 10.1002/cam4.1906. Epub 2019 Mar 1.

Abstract

The purpose of this retrospective study was to compare the efficacy and toxicity of high-dose methotrexate plus temozolomide (MT regimen) and rituximab plus MT (RMT regimen) in patients with untreated primary central nervous system lymphoma (PCNSL). A total of 62 patients with untreated PCNSL were enrolled between January 2005 and December 2015, with the median age of 53.5 years (range 29-77).In this study, 32 patients received RMT as induction therapy, and 30 received MT. Objective responses were noted in 93.7% of the patients in the RMT group and in 69.0% of the patients in the MT group (P = 0.018), while complete responses were noted in 53.2% of the patients in the RMT group and 27.6% of the patients in the MT group (P < 0.001). The 2- and 5-year PFS rates were 81.3% and 53.3%, respectively, for the RMT group and 46.5% and 29.1%, respectively, for the MT group (P = 0.019). The 2- and 5-year overall survival (OS) rates were 82.3% and 82.3%, respectively, for the RMT group and 65.7% and 50.0%, respectively, for the MT group (P = 0.015). Multivariate analyses showed that therapeutic regimen (RMT vs MT) was an independent prognostic factor for PFS and OS. Our encouraging results suggest that the RMT regimen may be a feasible and safe therapeutic approach for first-line treatment of PCNSL.

摘要

本回顾性研究旨在比较大剂量甲氨蝶呤联合替莫唑胺(MT 方案)与利妥昔单抗联合 MT(RMT 方案)治疗未经治疗的原发性中枢神经系统淋巴瘤(PCNSL)的疗效和毒性。2005 年 1 月至 2015 年 12 月期间共纳入 62 例未经治疗的 PCNSL 患者,中位年龄为 53.5 岁(范围 29-77 岁)。本研究中,32 例患者接受 RMT 作为诱导治疗,30 例患者接受 MT。RMT 组患者的客观缓解率为 93.7%,MT 组患者的客观缓解率为 69.0%(P=0.018),而 RMT 组完全缓解率为 53.2%,MT 组完全缓解率为 27.6%(P<0.001)。RMT 组患者的 2 年和 5 年无进展生存率(PFS)分别为 81.3%和 53.3%,MT 组患者的 2 年和 5 年 PFS 率分别为 46.5%和 29.1%(P=0.019)。RMT 组患者的 2 年和 5 年总生存率(OS)分别为 82.3%和 82.3%,MT 组患者的 2 年和 5 年 OS 率分别为 65.7%和 50.0%(P=0.015)。多因素分析显示,治疗方案(RMT 与 MT)是 PFS 和 OS 的独立预后因素。我们的研究结果令人鼓舞,表明 RMT 方案可能是 PCNSL 一线治疗的一种可行且安全的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3ef/6488123/9104d8b0b55d/CAM4-8-1359-g001.jpg

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