Is more better? Increased doses of high dose methotrexate and addition of rituximab is associated with improved outcomes in a large primary CNS lymphoma cohort.

Prakirthi Yerram, Samantha N Reiss, Lisa Modelevsky, Lauren Schaff, Anne S Reiner, Katherine S Panageas, Christian Grommes
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引用次数: 2

Abstract

Background: Primary central nervous system lymphoma (PCNSL) is a rare and aggressive primary brain tumor. While high dose methotrexate (HDMTX) regimens remain standard of care, it remains unclear if optimization of HDMTX doses and the addition of rituximab provide clinical benefit. Over the last 30 years, standard care given at Memorial Sloan Kettering Cancer Center (MSKCC) has evolved, allowing the comparison of patients receiving different numbers of HDMTX doses and those treated with and without rituximab. The purpose of this study was to describe outcomes based on treatment pattern changes.

Methods: This single-center, retrospective, IRB-approved study at MSKCC included patients with immunocompetent PCNSL, age ≥18 years and diagnosed between 1/1983-12/2017. Overall survival (OS) was modeled from date of last HDMTX for analyses associating HDMTX and OS. Multivariable Cox regression models estimated hazard ratios (HR) and corresponding 95% confidence intervals (CI).

Results: There were 546 patients identified with newly diagnosed PCNSL. Median overall survival (mOS) of the entire population was 4.7 years (95% CI: 3.8-5.7 years); 3.3 years (95% CI: 2.7-3.9 years) in patients diagnosed prior to 2006 and 8.1 years (95% CI: 6.6-11.1 years) in patients diagnosed 2006 onwards. Patients receiving ≥6 doses of HDMTX had improved survival compared to those receiving <6 doses of HDMTX (mOS: 7.8 vs. 4.3 years; P=0.001). Patients receiving induction rituximab had improved OS compared to those who did not receive rituximab (mOS: 10.5 vs. 3.2 years; P<0.0001). Patients receiving ≥6 doses of HDMTX and rituximab had greatest mOS at 13 years, with a 70% reduction in death (HR =0.30; 95% CI: 0.19-0.47) adjusting for treatment era, sex, and recursive partitioning analysis (RPA) classes comprising age and karnofsky performance score (KPS).

Conclusions: OS for PCNSL has improved significantly over the last few decades. Patients seem to benefit with ≥6 doses of HDMTX and the addition of rituximab, an effect independent of treatment era, age, and KPS.

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越多越好吗?在一个大型原发性中枢神经系统淋巴瘤队列中,增加高剂量甲氨蝶呤和利妥昔单抗的剂量与改善预后相关。
背景:原发性中枢神经系统淋巴瘤(PCNSL)是一种罕见的侵袭性原发性脑肿瘤。虽然高剂量甲氨蝶呤(HDMTX)方案仍然是标准的治疗方案,但目前尚不清楚HDMTX剂量的优化和利妥昔单抗的加入是否能提供临床益处。在过去的30年里,纪念斯隆凯特琳癌症中心(MSKCC)的标准治疗已经发展,可以比较接受不同剂量HDMTX的患者以及接受和不接受利妥昔单抗治疗的患者。本研究的目的是描述基于治疗模式改变的结果。方法:这项在MSKCC进行的单中心、回顾性、irb批准的研究纳入了年龄≥18岁、诊断于1983年1月至2017年12月期间的免疫功能正常的PCNSL患者。总生存期(OS)从最后一次HDMTX的日期开始建模,以分析HDMTX和OS之间的关系。多变量Cox回归模型估计了风险比(HR)和相应的95%置信区间(CI)。结果:新诊断PCNSL患者546例。整个人群的中位总生存期(mOS)为4.7年(95% CI: 3.8-5.7年);2006年以前诊断的患者为3.3年(95% CI: 2.7-3.9年),2006年以后诊断的患者为8.1年(95% CI: 6.6-11.1年)。与接受HDMTX治疗的患者相比,接受≥6剂HDMTX治疗的患者的生存期提高了4.3年;P = 0.001)。与未接受利妥昔单抗的患者相比,接受诱导性利妥昔单抗的患者OS得到改善(mOS: 10.5 vs. 3.2年;结论:在过去的几十年里,PCNSL的操作系统有了显著的改进。患者似乎受益于≥6剂量的HDMTX和利妥昔单抗的加入,这种效果与治疗时间、年龄和KPS无关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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