Cancer Research and Biostatistics, Seattle, WA.
Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
J Natl Cancer Inst. 2020 Mar 1;112(3):238-246. doi: 10.1093/jnci/djz137.
Cancer screening is a complex process encompassing risk assessment, the initial screening examination, diagnostic evaluation, and treatment of cancer precursors or early cancers. Metrics that enable comparisons across different screening targets are needed. We present population-based screening metrics for breast, cervical, and colorectal cancers for nine sites participating in the Population-based Research Optimizing Screening through Personalized Regimens consortium.
We describe how selected metrics map to a trans-organ conceptual model of the screening process. For each cancer type, we calculated calendar year 2013 metrics for the screen-eligible target population (breast: ages 40-74 years; cervical: ages 21-64 years; colorectal: ages 50-75 years). Metrics for screening participation, timely diagnostic evaluation, and diagnosed cancers in the screened and total populations are presented for the total eligible population and stratified by age group and cancer type.
The overall screening-eligible populations in 2013 were 305 568 participants for breast, 3 160 128 for cervical, and 2 363 922 for colorectal cancer screening. Being up-to-date for testing was common for all three cancer types: breast (63.5%), cervical (84.6%), and colorectal (77.5%). The percentage of abnormal screens ranged from 10.7% for breast, 4.4% for cervical, and 4.5% for colorectal cancer screening. Abnormal breast screens were followed up diagnostically in almost all (96.8%) cases, and cervical and colorectal were similar (76.2% and 76.3%, respectively). Cancer rates per 1000 screens were 5.66, 0.17, and 1.46 for breast, cervical, and colorectal cancer, respectively.
Comprehensive assessment of metrics by the Population-based Research Optimizing Screening through Personalized Regimens consortium enabled systematic identification of screening process steps in need of improvement. We encourage widespread use of common metrics to allow interventions to be tested across cancer types and health-care settings.
癌症筛查是一个复杂的过程,包括风险评估、初始筛查检查、诊断评估以及癌症前体或早期癌症的治疗。需要能够比较不同筛查目标的指标。我们为参与基于人群的研究优化个性化治疗方案通过个人化方案联盟的 9 个地点的乳腺癌、宫颈癌和结直肠癌展示基于人群的筛查指标。
我们描述了选定的指标如何映射到筛查过程的跨器官概念模型。对于每种癌症类型,我们计算了 2013 年筛查合格目标人群(乳腺癌:40-74 岁;宫颈癌:21-64 岁;结直肠癌:50-75 岁)的历年指标。我们为筛查参与、及时诊断评估以及筛查和总人群中诊断出的癌症呈现了筛查合格总人群以及按年龄组和癌症类型分层的指标。
2013 年,总体筛查合格人群分别为乳腺癌 305568 人、宫颈癌 3160128 人和结直肠癌 2363922 人。三种癌症类型的检测更新率都很高:乳腺癌(63.5%)、宫颈癌(84.6%)和结直肠癌(77.5%)。异常筛查的比例分别为乳腺癌 10.7%、宫颈癌 4.4%和结直肠癌 4.5%。异常的乳房筛查几乎都进行了诊断性随访(96.8%),而宫颈癌和结直肠癌类似(分别为 76.2%和 76.3%)。每 1000 次筛查的癌症发生率分别为乳腺癌 5.66、宫颈癌 0.17 和结直肠癌 1.46。
基于人群的研究优化个性化治疗方案联盟对指标进行全面评估,使我们能够系统地确定需要改进的筛查过程步骤。我们鼓励广泛使用通用指标,以便在癌症类型和医疗保健环境中测试干预措施。