Yang Wuyang, Garzon-Muvdi Tomas, Braileanu Maria, Porras Jose L, Caplan Justin M, Rong Xiaoming, Huang Judy, Jallo George I
Department of Neurosurgery, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Georgetown University Hospital/Washington Hospital Center Internal Medicine Residency Program, Medstar Georgetown University Hospital, Washington DC, USA.
Neuro Oncol. 2017 Mar 1;19(3):414-421. doi: 10.1093/neuonc/now178.
Primary intramedullary spinal cord lymphoma (PISCL) is a rare diagnosis with poorly understood disease progression. Clarification of the factors associated with survival in PISCL patients is warranted.
We conducted a population-based cohort study utilizing prospectively collected data from the Surveillance, Epidemiology, and End Results (SEER) database. Patients with histological diagnosis of primary lymphoma in spinal cord (C72.0) from 1973 to 2012 in the SEER database were included. Multivariable survival analysis between patient, lesion characteristics, and PISCL-related death was performed to adjust for confounding factors.
We included 346 PISCL patients in our study. Average age was 56.5 ± 17.8 years, with 62.7% being male. Racial distribution of these patients was white (87.6%), black (8.0%), and other (4.3%). More than half (55.8%) of patients were married. The most prevalent histology of PISCL was diffuse B-cell (46.2%), and the majority (55.2%) were low stage (Ann Arbor stage I/II). Most patients (67.9%) received radiation therapy. Average survival interval of patients with PISCL-related death (n=135, 39.0%) was 27.8 months. General cumulative survival probability at 1 year, 2 years, and 5 years was 73.8%, 67.9%, and 63.1%, respectively. Multivariable accelerated failure time (AFT) regression showed follicular lymphoma (HR:0.25, P=.008) and more recent diagnosis (HR:0.96, P<.001) was positively associated with PISCL-related survival. Conversely, nonwhite race (HR:1.69, P=.046), older age (HR:1.02, P<.001), unmarried status (HR:2.14, P<.001), and higher stage (HR:1.54, P=.022) were negatively associated with survival.
Age, race, marital status, tumor histology, tumor stage, and year of diagnosis were associated with survival of PISCL. While most PISCL-related deaths occur within a 1-year period, subsequent slow progression was observed after the first year of survival.
原发性脊髓内淋巴瘤(PISCL)是一种罕见的疾病,其疾病进展情况尚不清楚。有必要明确与PISCL患者生存相关的因素。
我们利用监测、流行病学和最终结果(SEER)数据库中前瞻性收集的数据进行了一项基于人群的队列研究。纳入了1973年至2012年SEER数据库中组织学诊断为脊髓原发性淋巴瘤(C72.0)的患者。对患者、病变特征和PISCL相关死亡之间进行多变量生存分析,以调整混杂因素。
我们的研究纳入了346例PISCL患者。平均年龄为56.5±17.8岁,男性占62.7%。这些患者的种族分布为白人(87.6%)、黑人(8.0%)和其他(4.3%)。超过一半(55.8%)的患者已婚。PISCL最常见的组织学类型是弥漫性B细胞(46.2%),大多数(55.2%)为低分期(Ann Arbor分期I/II)。大多数患者(67.9%)接受了放射治疗。PISCL相关死亡患者(n = 135,39.0%)的平均生存间隔为27.8个月。1年、2年和5年的总体累积生存概率分别为73.8%、67.9%和63.1%。多变量加速失效时间(AFT)回归显示滤泡性淋巴瘤(HR:0.25,P = 0.008)和更近的诊断时间(HR:0.96,P < 0.001)与PISCL相关生存呈正相关。相反,非白人种族(HR:1.69,P = 0.046)、年龄较大(HR:1.02,P <