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Samples were considered positive if they attained or exceeded the FDA approved threshold of 1.0 pg HPV DNA/mL.
The US Food and Drug Administration approved threshold of 1 pg of HPV DNA ml−1 of test solution was the positive control.
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Samples were considered positive if they attained or exceeded the FDA-approved threshold of 1.0 pg HPV DNA ml−1, which corresponds to 1.0 relative light units (RLU).
Samples were considered positive if they attained or exceeded the FDA-approved threshold of 1.0 pg HPV DNA/ml, which corresponds to 1.0 relative light unit (RLU).
An HPV-HC2 result was considered positive when it attained or exceeded the FDA-approved threshold of 1.0 pg HPV DNA ml−1, which corresponds to 1.0 RLU.
An HPV sample was considered positive if it attained or exceeded the Federal Drug Administration (FDA -approved threshold oFDA -approvedDNA ml-1, which corresponds thresholdlative light unit (RLU/Cof.
An HPV sample was considered positive if attained or exceeded the FDA-approved threshold of 1.0 pg HPV DNA ml−1, which corresponds to 1.0 relative light unit (RLU/CO).
Although the delineated threshold for survival varies across studies from 3 to 5 CTCs [ 9– 11, 24, 31, 34, 36– 38] in our study the FDA-approved threshold for therapy monitoring of <5 vs. ≥5 CTCs was applicable as a predictor of treatment efficacy in our cohort.
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