Carolyn M Rutter, Pedro Nascimento de Lima, Jeffrey K Lee, Jonathan Ozik
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We examined how well the model predicted outcomes measured over a three-year follow-up period, including the number of adenomas detected, the size of the largest adenoma detected, and incident colorectal cancer.</p><p><strong>Results: </strong>Using standard sensitivity assumptions, the model predicted adenoma prevalence that was too low (42.5% versus 48.9% observed, with 95% confidence interval 45.3%-50.7%) and detection of too few large adenomas (5.1% versus 14.% observed, with 95% confidence interval 11.8%-17.4%). Predictions were close to targets when we set sensitivities to 0.20 for diminutive adenomas, 0.60 for small adenomas, 0.80 for 10- to 20-mm adenomas, and 0.98 for adenomas 20 mm and larger.</p><p><strong>Conclusions: </strong>Colonoscopy may be less accurate than currently assumed, especially for diminutive adenomas. Alternatively, the CRC-SPIN model may not accurately simulate onset and progression of adenomas in higher-risk populations.</p><p><strong>Impact: </strong>Misspecification of either colonoscopy sensitivity or disease progression in high-risk populations may affect the predicted effectiveness of colorectal cancer screening. When possible, decision analyses used to inform policy should address these uncertainties.See related commentary by Etzioni and Lange, p. 702.</p>","PeriodicalId":520580,"journal":{"name":"Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology","volume":" ","pages":"775-782"},"PeriodicalIF":0.0000,"publicationDate":"2022-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8983491/pdf/nihms-1762910.pdf","citationCount":"2","resultStr":"{\"title\":\"Too Good to Be True? 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We examined how well the model predicted outcomes measured over a three-year follow-up period, including the number of adenomas detected, the size of the largest adenoma detected, and incident colorectal cancer.</p><p><strong>Results: </strong>Using standard sensitivity assumptions, the model predicted adenoma prevalence that was too low (42.5% versus 48.9% observed, with 95% confidence interval 45.3%-50.7%) and detection of too few large adenomas (5.1% versus 14.% observed, with 95% confidence interval 11.8%-17.4%). Predictions were close to targets when we set sensitivities to 0.20 for diminutive adenomas, 0.60 for small adenomas, 0.80 for 10- to 20-mm adenomas, and 0.98 for adenomas 20 mm and larger.</p><p><strong>Conclusions: </strong>Colonoscopy may be less accurate than currently assumed, especially for diminutive adenomas. Alternatively, the CRC-SPIN model may not accurately simulate onset and progression of adenomas in higher-risk populations.</p><p><strong>Impact: </strong>Misspecification of either colonoscopy sensitivity or disease progression in high-risk populations may affect the predicted effectiveness of colorectal cancer screening. 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引用次数: 2
摘要
背景:模型可以帮助指导结直肠癌筛查政策。尽管模型经过仔细校准和验证,但对测试性能的假设审查较少。方法:我们检验了CRC-SPIN模型和结肠镜敏感性假设的有效性。标准敏感性假设与已发表的决策分析一致,假设小型腺瘤的敏感性为0.75(结果:使用标准敏感性假设,该模型预测腺瘤的患病率过低(42.5% vs 48.9%观察值,95%置信区间为45.3%-50.7%)和检测到的大型腺瘤太少(5.1% vs 14)。%, 95%可信区间为11.8% ~ 17.4%)。当我们将敏感性设置为小腺瘤0.20,小腺瘤0.60,10- 20毫米腺瘤0.80,20毫米及以上腺瘤0.98时,预测接近目标。结论:结肠镜检查的准确性可能低于目前所认为的,特别是对于小腺瘤。另外,CRC-SPIN模型可能无法准确模拟高危人群中腺瘤的发生和进展。影响:在高危人群中,结肠镜敏感性或疾病进展的错误描述可能会影响结肠直肠癌筛查的预期效果。在可能的情况下,用于为政策提供信息的决策分析应解决这些不确定性。参见Etzioni和Lange的相关评论,第702页。
Too Good to Be True? Evaluation of Colonoscopy Sensitivity Assumptions Used in Policy Models.
Background: Models can help guide colorectal cancer screening policy. Although models are carefully calibrated and validated, there is less scrutiny of assumptions about test performance.
Methods: We examined the validity of the CRC-SPIN model and colonoscopy sensitivity assumptions. Standard sensitivity assumptions, consistent with published decision analyses, assume sensitivity equal to 0.75 for diminutive adenomas (<6 mm), 0.85 for small adenomas (6-10 mm), 0.95 for large adenomas (≥10 mm), and 0.95 for preclinical cancer. We also selected adenoma sensitivity that resulted in more accurate predictions. Targets were drawn from the Wheat Bran Fiber study. We examined how well the model predicted outcomes measured over a three-year follow-up period, including the number of adenomas detected, the size of the largest adenoma detected, and incident colorectal cancer.
Results: Using standard sensitivity assumptions, the model predicted adenoma prevalence that was too low (42.5% versus 48.9% observed, with 95% confidence interval 45.3%-50.7%) and detection of too few large adenomas (5.1% versus 14.% observed, with 95% confidence interval 11.8%-17.4%). Predictions were close to targets when we set sensitivities to 0.20 for diminutive adenomas, 0.60 for small adenomas, 0.80 for 10- to 20-mm adenomas, and 0.98 for adenomas 20 mm and larger.
Conclusions: Colonoscopy may be less accurate than currently assumed, especially for diminutive adenomas. Alternatively, the CRC-SPIN model may not accurately simulate onset and progression of adenomas in higher-risk populations.
Impact: Misspecification of either colonoscopy sensitivity or disease progression in high-risk populations may affect the predicted effectiveness of colorectal cancer screening. When possible, decision analyses used to inform policy should address these uncertainties.See related commentary by Etzioni and Lange, p. 702.