Bairey Osnat, Lebel Eyal, Buxbaum Chen, Porges Tzvika, Taliansky Alisa, Gurion Ronit, Goldschmidt Neta, Shina Tzahala Tzuk, Zektser Miri, Hofstetter Liron, Siegal Tali
Institute of Hematology, Davidoff Cancer Center, Rabin Medical Center, Petach Tikva, Israel.
Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Hematol Oncol. 2023 Dec;41(5):838-847. doi: 10.1002/hon.3198. Epub 2023 Jul 5.
Primary central nervous system lymphoma (PCNSL) is a rare disease with an incidence of 0.4/per 100,000 person-years. As there is a limited number of prospective randomized trials in PCNSL, large retrospective studies on this rare disease may yield information that might prove useful for the future design of randomized clinical trials. We retrospectively analyzed the data of 222 newly diagnosed PCNSL patients treated in five referral centers in Israel between 2001 and 2020. During this period, combination therapy became the treatment of choice, rituximab has been added to the induction therapy, and consolidation with irradiation was largely laid off and was mostly replaced by high-dose chemotherapy with or without autologous stem cell transplantation (HDC-ASCT). Patients older than 60 comprised 67.5% of the study population. First-line treatment included high-dose methotrexate (HD-MTX) in 94% of patients with a median MTX dose of 3.5 g/m (range 1.14-6 g/m ) and a median cycle number of 5 (range 1-16). Rituximab was given to 136 patients (61%) and consolidation treatment to 124 patients (58%). Patients treated after 2012 received significantly more treatment with HD-MTX and rituximab, more consolidation treatments, and autologous stem cell transplantation. The overall response rate was 85% and the complete response (CR)/unconfirmed CR rate was 62.1%. After a median follow-up of 24 months, the median progression-free survival (PFS) and overall survival (OS) were 21.9 and 43.5 months respectively with a significant improvement since 2012 (PFS: 12.5 vs. 34.2 p = 0.006 and OS: 19.9 vs. 77.3 p = 0.0003). A multivariate analysis found that the most important factors related to OS were obtaining a CR followed by rituximab treatment and Eastern Cooperative Oncology Group performance status. The observed improvement in outcomes may be due to multiple components such as an intention to treat all patients regardless of age with HD-MTX-based combination chemotherapy, treatment in dedicated centers, and more aggressive consolidation with the introduction of HDC-ASCT.
原发性中枢神经系统淋巴瘤(PCNSL)是一种罕见疾病,发病率为每10万人年0.4例。由于PCNSL的前瞻性随机试验数量有限,针对这种罕见疾病的大型回顾性研究可能会产生一些信息,这些信息可能对未来随机临床试验的设计有用。我们回顾性分析了2001年至2020年期间在以色列五个转诊中心接受治疗的222例新诊断PCNSL患者的数据。在此期间,联合治疗成为首选治疗方法,利妥昔单抗已被添加到诱导治疗中,放疗巩固治疗基本被放弃,大多被有或无自体干细胞移植(HDC-ASCT)的大剂量化疗所取代。60岁以上患者占研究人群的67.5%。一线治疗包括94%的患者使用大剂量甲氨蝶呤(HD-MTX),甲氨蝶呤中位剂量为3.5g/m²(范围1.14-6g/m²),中位疗程数为5(范围1-16)。136例患者(61%)接受了利妥昔单抗治疗,124例患者(58%)接受了巩固治疗。2012年后接受治疗的患者接受HD-MTX和利妥昔单抗治疗、巩固治疗以及自体干细胞移植的比例显著更高。总缓解率为85%,完全缓解(CR)/未确认CR率为62.1%。中位随访24个月后,中位无进展生存期(PFS)和总生存期(OS)分别为21.9个月和43.5个月,自2012年以来有显著改善(PFS:12.5对34.2,p = 0.006;OS:19.9对77.3,p = 0.0003)。多变量分析发现,与OS相关的最重要因素是获得CR,其次是利妥昔单抗治疗和东部肿瘤协作组体能状态。观察到的预后改善可能归因于多个因素,如使用基于HD-MTX的联合化疗治疗所有患者(无论年龄)的意向、在专门中心进行治疗以及引入HDC-ASCT后更积极的巩固治疗。