Department of Hematology, Tel Aviv Sourasky Medical Center, 6 Weizmann Street, 6423906, Tel Aviv, Israel.
Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
J Neurooncol. 2021 Jan;151(2):211-220. doi: 10.1007/s11060-020-03654-x. Epub 2020 Oct 24.
Primary central nervous system lymphoma (PCNSL) is a rare disease with a dismal prognosis compared to its systemic large B-cell lymphoma counterpart. Real world data are limited, when considering a uniform backbone treatment.
A retrospective study of all adult patients treated sequentially with a high-dose methotrexate (HD MTX)-based regimen in a single tertiary medical center between 2003 and 2019.
The 2015-2019 period differed from its predecessor in that most patients were treated with an HD MTX-based polychemotherapy regimen as opposed to HD MTX monotherapy (81% vs. 13%, P < .001), rituximab was given as standard of care (100% vs. 56%, P < .01), and most induction-responsive patients received consolidation treatment (70% vs. 18%, P = .01). The median progression-free and overall survival (OS) for the entire cohort (n = 73, mean age 64 years) was 9.9 and 29.8 months, respectively. Patients diagnosed between 2015 and 2019 had superior OS (P = .03) compared to those treated earlier. An interim partial response (PR) state, documented after two cycles of chemotherapy, was associated with increased incidence of progression, with only 33% of those patients achieving end-of-induction complete response. Twenty-three percent of patients developed thrombotic events and 44% developed grade 3-4 infections. HD MTX-based polychemotherapy induction was associated with both increase in thrombotic and infection incidence.
Contemporary HD MTX-based combination therapies suggestively improved the outcomes for PCNSL, but at a cost of increased incidence of toxicity. Patients who achieve an interim PR status are at a high risk for treatment failure.
原发性中枢神经系统淋巴瘤(PCNSL)与全身大 B 细胞淋巴瘤相比,预后较差,是一种罕见疾病。在考虑统一的基础治疗时,实际数据有限。
对 2003 年至 2019 年期间在一家三级医学中心连续接受高剂量甲氨蝶呤(HD MTX)为基础的方案治疗的所有成年患者进行回顾性研究。
2015-2019 年与前一时期的不同之处在于,大多数患者接受 HD MTX 为基础的联合化疗方案治疗,而非 HD MTX 单药治疗(81%对 13%,P<0.001),利妥昔单抗作为标准治疗(100%对 56%,P<0.01),大多数诱导反应患者接受巩固治疗(70%对 18%,P=0.01)。整个队列(n=73,平均年龄 64 岁)的中位无进展生存期和总生存期分别为 9.9 和 29.8 个月。2015 年至 2019 年间诊断的患者的 OS 优于早期治疗的患者(P=0.03)。化疗两个周期后记录的部分缓解(PR)状态与进展发生率增加相关,只有 33%的患者达到诱导结束时的完全缓解。23%的患者发生血栓事件,44%的患者发生 3-4 级感染。HD MTX 为基础的联合化疗诱导与血栓形成和感染发生率的增加有关。
当代 HD MTX 为基础的联合治疗方案提示改善了 PCNSL 的预后,但毒性发生率增加。达到中期 PR 状态的患者治疗失败的风险很高。