Yerram Prakirthi, Reiss Samantha N, Modelevsky Lisa, Schaff Lauren, Reiner Anne S, Panageas Katherine S, Grommes Christian
Department of Pharmacy, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Department of Neurology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Ann Lymphoma. 2023 Feb 28;7. doi: 10.21037/aol-22-19.
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.
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).
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 4.3 years; P=0.001). Patients receiving induction rituximab had improved OS compared to those who did not receive rituximab (mOS: 10.5 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).
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.
原发性中枢神经系统淋巴瘤(PCNSL)是一种罕见且侵袭性强的原发性脑肿瘤。虽然高剂量甲氨蝶呤(HDMTX)方案仍是标准治疗方法,但HDMTX剂量的优化以及联合使用利妥昔单抗是否能带来临床益处仍不明确。在过去30年中,纪念斯隆凯特琳癌症中心(MSKCC)的标准治疗方法不断演变,这使得我们能够比较接受不同剂量HDMTX治疗的患者以及接受或未接受利妥昔单抗治疗的患者。本研究的目的是根据治疗模式的变化描述治疗结果。
这项在MSKCC进行的单中心、回顾性、经机构审查委员会(IRB)批准的研究纳入了年龄≥18岁、在1983年1月至2017年12月期间确诊的免疫功能正常的PCNSL患者。总生存期(OS)从最后一次HDMTX治疗日期开始建模,用于分析HDMTX与OS之间的关系。多变量Cox回归模型估计风险比(HR)和相应的95%置信区间(CI)。
共确定546例新诊断的PCNSL患者。整个人群的中位总生存期(mOS)为4.7年(95%CI:3.8 - 5.7年);2006年前确诊的患者为3.3年(95%CI:2.7 - 3.9年),2006年及以后确诊的患者为8.1年(95%CI:6.6 - 11.1年)。接受≥6剂HDMTX治疗的患者与接受<6剂HDMTX治疗的患者相比,生存期有所改善(mOS:7.8对4.3年;P = 0.001)。接受诱导性利妥昔单抗治疗的患者与未接受利妥昔单抗治疗的患者相比,OS有所改善(mOS:10.5对3.2年;P < 0.0001)。接受≥6剂HDMTX和利妥昔单抗治疗的患者mOS最长,为13年,校正治疗时代、性别以及包含年龄和卡诺夫斯基性能评分(KPS)的递归分区分析(RPA)类别后,死亡风险降低70%(HR = 0.30;95%CI:0.19 - 0.47)。
在过去几十年中,PCNSL的OS有了显著改善。患者似乎从≥6剂HDMTX治疗以及联合使用利妥昔单抗中获益,这种效果与治疗时代、年龄和KPS无关。