Farrall Alexandra L, Smith Justine R
College of Medicine & Public Health, Flinders University, Bedford Park, SA 5042, Australia.
Cancers (Basel). 2021 Jan 22;13(3):403. doi: 10.3390/cancers13030403.
Primary central nervous system lymphoma (PCNSL) is a rare brain cancer that remains challenging to study. Epidemiology of PCNSL in the Australian population, which is racially and ethnically diverse, has not been examined previously. Using ICD-O-3.1 Morphology and Topography Codes to identify cases, we analyzed complete datasets from the comprehensive Australian Cancer Database (1982-2014, adults aged ≥ 20 years) to establish incidence rates and trends of PCNSL, and to define survival outcomes of individuals diagnosed with PCNSL, including the predominant diffuse large B-cell lymphoma (DLBCL) type. Age-standardized incidence of PCNSL increased by an average annual 6.8% percent over the study period, with current incidence of 0.43 (95% confidence interval, 0.41-0.46) per 100,000 person-years, in comparison to 21.89 (21.41-22.38) per 100,000 person-years for non-CNS lymphoma. Increase in incidence was characterized by an acute rise between 1996 and 1999, was more pronounced with increasing age, and was driven by increasing incidence of DLBCL. Overall survival for persons diagnosed with PCNSL improved significantly across the study period, with 5-year survival probability increasing from 0.21 (95% confidence interval, 0.16-0.26) to 0.33 (0.30-0.36), and median survival increasing from 318 to 600 days, between 1982-1999 and 2000-2014. Increase in survival was significantly higher for persons with DLBCL versus non-DLBCL PCNSL, but substantially lower than that for persons with non-CNS lymphoma, who had a 5-year survival probability of 0.62 (0.62-0.62) and a median survival of 3388 days in 2000-2014. This study links increasing incidence of PCNSL in Australia to increasing incidence of DLCBL, including in younger adults, and highlights the improving, but low, survival outcome of this cancer.
原发性中枢神经系统淋巴瘤(PCNSL)是一种罕见的脑癌,其研究仍具有挑战性。此前尚未对种族和民族多样化的澳大利亚人群中的PCNSL流行病学进行过研究。我们使用国际疾病分类肿瘤学第三版(ICD - O - 3.1)形态学和部位编码来识别病例,分析了来自澳大利亚综合癌症数据库(1982 - 2014年,年龄≥20岁的成年人)的完整数据集,以确定PCNSL的发病率和趋势,并确定被诊断为PCNSL的个体的生存结果,包括主要的弥漫性大B细胞淋巴瘤(DLBCL)类型。在研究期间,PCNSL的年龄标准化发病率平均每年增长6.8%,目前的发病率为每10万人年0.43(95%置信区间,0.41 - 0.46),而非中枢神经系统淋巴瘤的发病率为每10万人年21.89(21.41 - 22.38)。发病率的增加表现为1996年至1999年之间的急剧上升,随着年龄增长更为明显,并且是由DLBCL发病率的增加所驱动。在整个研究期间,被诊断为PCNSL的人的总体生存率有显著提高,5年生存概率从0.21(95%置信区间,0.16 - 0.26)提高到0.33(0.30 - 0.36),中位生存期从1982 - 1999年的318天增加到2000 - 2014年的600天。与非DLBCL型PCNSL患者相比,DLBCL型PCNSL患者的生存率提高更为显著,但远低于非中枢神经系统淋巴瘤患者,2000 - 2014年非中枢神经系统淋巴瘤患者的5年生存概率为0.62(0.62 - 0.62),中位生存期为3388天。这项研究将澳大利亚PCNSL发病率的增加与DLCBL发病率的增加联系起来,包括在年轻成年人中,并强调了这种癌症的生存结果虽在改善但仍较低。