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A novel metric that quantifies risk stratification for evaluating diagnostic tests: The example of evaluating cervical-cancer screening tests across populations

机译:一种新的度量,量化用于评估诊断试验的风险分层:跨种群评估宫颈癌筛查试验的实施例

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Our work involves assessing whether new biomarkers might be useful for cervical-cancer screening across populations with different disease prevalences and biomarker distributions. When comparing across populations, we show that standard diagnostic accuracy statistics (predictive values, risk-differences, Youden's index and Area Under the Curve (AUC)) can easily be misinterpreted. We introduce an intuitively simple statistic for a 2x2 table, Mean Risk Stratification (MRS): the average change in risk (pre-test vs. post-test) revealed for tested individuals. High MRS implies better risk separation achieved by testing. MRS has 3 key advantages for comparing test performance across populations with different disease prevalences and biomarker distributions. First, MRS demonstrates that conventional predictive values and the risk-difference do not measure risk-stratification because they do not account for test-positivity rates. Second, Youden's index and AUC measure only multiplicative relative gains in risk-stratification: AUC=0.6 achieves only 20% of maximum risk-stratification (AUC= 0.9 achieves 80%). Third, large relative gains in risk-stratification might not imply large absolute gains if disease is rare, demonstrating a "high-bar" to justify population-based screening for rare diseases such as cancer. We illustrate MRS by our experience comparing the performance of cervical-cancer screening tests in China vs. the USA. The test with the worst AUC= 0.72 in China (visual inspection with acetic acid) provides twice the risk-stratification (i.e. MRS) of the test with best AUC= 0.83 in the USA (human papillomavirus and Pap cotesting) because China has three times more cervical precancer/cancer. MRS could be routinely calculated to better understand the clinical/public-health implications of standard diagnostic accuracy statistics.
机译:我们的作品涉及评估新的生物标志物在具有不同疾病患病率和生物标志物分布的群体中可能对宫颈癌筛查有用。在跨人群比较时,我们表明标准诊断准确性统计数据(预测值,风险差异,YENDEN(AUC)下的指数和面积)很容易被误解。我们为2x2表进行了直观的简单统计,均值风险分层(MRS):用于测试个体的风险的平均风险变化(测试前试验前测试)。 High MRS意味着通过测试实现的更好的风险分离。 MRS有3个关键优势,可以在具有不同疾病普遍和生物标志物分布的群体中进行比较。首先,MRS展示了传统的预测值和风险差异不测量风险分层,因为它们不考虑测试积极率。其次,YENDEN的指数和AUC措施只有风险分层的乘法相对增益:AUC = 0.6达到最大风险分层的20%(AUC = 0.9达到80%)。第三,如果疾病罕见,风险分层的风险分层的相对增益可能并不意味着,如果疾病罕见,则证明“高级”,以证明基于人群的筛查诸如癌症等稀有疾病的筛查。我们通过我们的经验说明了MRS,比较了中国宫颈癌筛查试验的表现与美国。中国最差AUC = 0.72的试验(用醋酸的目视检查)提供了两倍于美国(人乳头瘤病毒和PAP COTESTING)的最佳AUC = 0.83的试验的风险分层(即MRS),因为中国有三次更多宫颈癌/癌症。 MRS可以常规地计算以更好地了解标准诊断准确统计的临床/公共健康影响。

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