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2010年至2015年在加拿大4个省份诊断出的原发性中枢神经系统肿瘤的发病率和生存率。

Incidence and survival of primary central nervous system tumors diagnosed in 4 Canadian provinces from 2010 to 2015.

作者信息

Walker Emily V, Davis Faith G, Yasmin Farzana, Smith Trenton R, Yuan Yan

机构信息

School of Public Health, University of Alberta, Alberta, Canada.

Surveillance and Reporting, Advanced Analytics, Cancer Research and Analytics, Cancer Care Alberta, Alberta Health Services, Alberta, Canada.

出版信息

Neurooncol Pract. 2022 Nov 26;10(2):203-213. doi: 10.1093/nop/npac089. eCollection 2023 Apr.

Abstract

BACKGROUND

The Brain Tumor Registry of Canada was established in 2016 to enhance infrastructure for surveillance and clinical research on Central Nervous System (CNS) tumors. We present information on primary CNS tumors diagnosed among residents of Canada from 2010 to 2015.

METHODS

Data from 4 provincial cancer registries were analyzed representing approximately 67% of the Canadian population. Age-standardized incidence rates (ASIR) and 95% confidence intervals (CI) were calculated using the 2011 Canadian population age distribution. Net survival was estimated using the Pohar-Perme method.

RESULTS

A total of 31 644 primary tumors were identified for an ASIR of 22.8 per 100 000 person-years. Nonmalignant tumors made up 47.1% of all classified tumors, with mixed behaviors present in over half of histology groupings. Unclassified were 19.5% of all tumors. The most common histological subtypes are meningiomas (ASIR = 5.5 per 100 000 person-years); followed by glioblastomas (ASIR 4.0 per 100 000 person-years). The overall 5-year net survival rate for CNS tumors was 65.5%; females 70.2% and males 60.4%. GBMs continue to be the most lethal CNS tumors for all sex and age groups.

CONCLUSIONS

The low annual frequency of most CNS tumor subtypes emphasizes the value of population-based data on all primary CNS tumors diagnosed among Canadians. The large number of histological categories including mixed behaviors and the proportion of unclassified tumors emphasizes the need for complete reporting. Variation in incidence and survival across histological groups by sex and age highlights the need for comprehensive and histology-specific reporting. These data can be used to better inform research and health system planning.

摘要

背景

加拿大脑肿瘤登记处成立于2016年,旨在加强中枢神经系统(CNS)肿瘤监测和临床研究的基础设施。我们提供了2010年至2015年加拿大居民中诊断出的原发性中枢神经系统肿瘤的信息。

方法

分析了来自4个省级癌症登记处的数据,这些数据约占加拿大人口的67%。使用2011年加拿大人口年龄分布计算年龄标准化发病率(ASIR)和95%置信区间(CI)。采用波哈尔-珀梅方法估计净生存率。

结果

共识别出31644例原发性肿瘤,年龄标准化发病率为每10万人年22.8例。非恶性肿瘤占所有分类肿瘤的47.1%,超过一半的组织学分组存在混合行为。未分类的占所有肿瘤的19.5%。最常见的组织学亚型是脑膜瘤(年龄标准化发病率为每10万人年5.5例);其次是胶质母细胞瘤(年龄标准化发病率为每10万人年4.0例)。中枢神经系统肿瘤的总体5年净生存率为65.5%;女性为70.2%,男性为60.4%。胶质母细胞瘤仍然是所有性别和年龄组中最致命的中枢神经系统肿瘤(GBMs)。

结论

大多数中枢神经系统肿瘤亚型的年发病率较低,这凸显了基于人群的加拿大所有原发性中枢神经系统肿瘤诊断数据的价值。大量的组织学类别,包括混合行为和未分类肿瘤的比例,强调了完整报告的必要性。不同组织学组在发病率和生存率上的性别和年龄差异凸显了全面和特定组织学报告的必要性。这些数据可用于更好地为研究和卫生系统规划提供信息。

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