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. Author manuscript; available in PMC: 2023 Aug 2.
Published in final edited form as: Cancer Epidemiol Biomarkers Prev. 2022 Aug 2;31(8):1517–1520. doi: 10.1158/1055-9965.EPI-22-0232

Table 3.

Hypothetical example of the impact on estimated sensitivity and specificity of using different accuracy assessment interval lengths

Unobserved truth
Cancer No cancer Total
Screen + 8 20 28
Screen − 2 970 972
Total 10 990 1000
Sensitivity 80.0%
Specificity 98.0%
Observed with 6-month accuracy assessment interval
Cancer No cancer Total TP misclassified as FP 2.400
Screen + 5.604 22.396 28 TN misclassified as FN 0.194
Screen − 2.194 969.806 972 FP misclassified as TP 0.004
Total 7.798 992.202 1000 FN misclassified as TN 0
Sensitivity 71.9%
Specificity 97.7%
Observed with 12-month accuracy assessment interval
Total Cancer No cancer Total TP misclassified as FP 0.800
Screen + 7.210 20.790 28 TN misclassified as FN 0.485
Screen − 2.485 969.515 972 FP misclassified as TP 0.010
Total 9.695 990.305 1000 FN misclassified as TN 0
Sensitivity 74.4%
Specificity 97.9%

FP=false positive; FN=false negative; TP=true positive; TN=true negative

1

We assume that during a 6-month accuracy assessment interval, 0.02% of the no-cancer group develops and is diagnosed with cancer and that 70% of the screen-positive group receives a cancer-confirming follow-up test.

2

We assume that during a 12-month accuracy assessment interval 0.05% of the no-cancer group develops and is diagnosed with cancer and that 90% of the screen-positive group receives a cancer-confirming follow-up test.