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Longitudinal Screening Algorithm That Incorporates Change Over Time in CA125 Levels Identifies Ovarian Cancer Earlier Than a Single-Threshold Rule
Abstract
Purpose Longitudinal
algorithms incorporate change over time in biomarker levels to
individualize screening decision rules. Compared
with a single-threshold (ST) rule, smaller
deviations from baseline biomarker levels are required to signal
disease. We demonstrated
improvement in ovarian cancer early detection by
using a longitudinal algorithm to monitor annual CA125 levels.
Patients and Methods
We retrospectively evaluated serial preclinical serum CA125 values
measured annually in 44 incident ovarian cancer cases
identified from participants in the PLCO
(Prostate Lung Colorectal and Ovarian) Cancer Screening Trial to
determine how frequently
and to what extent the parametric empirical
Bayes (PEB) longitudinal screening algorithm identifies ovarian cancer
earlier
than an ST rule.
Results The PEB
algorithm detected ovarian cancer earlier than an ST rule in a
substantial proportion of cases. At 99% specificity,
which corresponded to the ST-rule CA125 cutoff ≥
35 U/mL that was used in the PLCO trial, 20% of cases were identified
earlier
by using the PEB algorithm. Among these cases,
the PEB signaled abnormal CA125 values, on average, 10 months earlier
and at
a CA125 concentration 42% lower (20 U/mL) than
the ST-rule cutoff. The proportion of cases detected earlier by the PEB
algorithm
and the earliness of detection increased as the
specificity of the screening rule was reduced.
Conclusion The PEB
longitudinal algorithm identifies ovarian cancer earlier and at lower
biomarker concentrations than an ST screening
algorithm adjusted to the same specificity.
Longitudinal biomarker assessment by using the PEB algorithm may have
application
for screening other solid tumors in which
biomarkers are available.
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