The Burden of Rare Cancers in North America.

Q4 Medicine Journal of registry management Pub Date : 2023-01-01
Brenda M Hofer, Hannah K Weir, Angela Eckstrand, Keisha Musonda, Recinda Sherman
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Abstract

Background: Rare cancers are difficult to study owing to their infrequent diagnosis. Using aggregate incidence data from population-based cancer registries in Europe, the Surveillance of Rare Cancers in Europe project compiled a list of clinically relevant, topography and morphology defined rare cancers operationally defined as having a crude annual incidence rate of <6 per 100,000 persons. In 2020, this list of rare cancers was updated. The objective of this study was to assess the utility of a rare cancer recode variable for use in the Cancer in North America (CiNA) dataset and to provide a first look at the burden of rare cancers in Canada and the United States.

Methods: Data were obtained from 62 registries in Canada and the United States that met North American Association of Central Cancer Registries (NAACCR) high-quality data standards. The list of rare cancers was programmed as a Rare Cancer Classification variable within SEER*Stat. SEER*Stat was used to estimate case counts and crude and age-specific incidence rates per 100,000 for cancers diagnosed 2015-2019 by age at diagnosis, country, and country-specific geographic regions in Canada and the United States, and by race/ethnicity in the United States.

Results: In Canada and the United States, 21% and 22% of all invasive cancers were classified as rare, respectively. The percentage of rare cancers ranged between 18% to 21% across geographic regions in Canada and the United States. Children (aged 0-14 years) had the highest percentage and lowest incidence rates of rare cancers. The percentage of rare cancers decreased, and incidence increased with increasing age. In the United States, Hispanics had the highest percentage (27%) and non-Hispanic Whites and non-Hispanic Blacks the lowest percentage (21%) of rare cancers.

Conclusions: While individual rare cancers are infrequently diagnosed, in aggregate, they account for a substantial percentage of all cancers diagnosed in the population and pose a substantial public health burden. We report variations in percentage of rare cancers by age, and race/ethnicity (United States only). Such variations in the burden of these cancers may suggest possible areas for public health research.

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北美罕见癌症的负担。
背景:由于罕见癌症很少被诊断出来,因此很难对其进行研究。欧洲罕见癌症监测项目利用欧洲基于人口的癌症登记处提供的总发病率数据,编制了一份与临床相关的、从地形和形态学角度界定的罕见癌症清单,该清单在操作上被定义为粗略年发病率为方法:数据来自加拿大和美国符合北美中央癌症登记处协会 (NAACCR) 高质量数据标准的 62 个登记处。罕见癌症列表被编程为 SEER*Stat 中的罕见癌症分类变量。SEER*Stat用于估算2015-2019年加拿大和美国按诊断年龄、国家和国家特定地理区域,以及美国按种族/族裔分列的每10万人中确诊癌症的病例数、粗发病率和特定年龄发病率:在加拿大和美国,分别有21%和22%的侵袭性癌症被归类为罕见癌症。在加拿大和美国的不同地区,罕见癌症的比例介于18%和21%之间。儿童(0-14 岁)患罕见癌症的比例最高,发病率最低。随着年龄的增长,罕见癌症的比例下降,发病率上升。在美国,西班牙裔患罕见癌症的比例最高(27%),非西班牙裔白人和非西班牙裔黑人患罕见癌症的比例最低(21%):虽然个别罕见癌症很少被诊断出来,但总体而言,它们在人口中诊断出的所有癌症中占了相当大的比例,并对公共健康造成了巨大负担。我们报告了不同年龄和种族/人种(仅美国)罕见癌症比例的差异。这些癌症负担的这种差异可能为公共卫生研究提供了可能的领域。
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来源期刊
Journal of registry management
Journal of registry management Medicine-Medicine (all)
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