Purpose: This study aimed to evaluate the performance of the PANArray human papilloma virus (HPV) test, a PCR-based DNA microarray assay, in detecting INV from patient samples and its concordance with the cobas 4800 HPV and Hybrid Capture 2 (HC2) tests. Materials and Methods: The PANArray HPV, cobas 4800 HPV, and HC2 tests were performed on 504 cervical swab samples from patients with atypical cells of undetermined significance at five hospitals. The samples that were interpreted as 'HPV-other' type positive in the PANArray HPV test were confirmed by direct sequencing. Results: 'the concordance rates were 80.8% between the cobas 4800 HPV and PANArray HPV tests [kappa=0.59, 95% confidence interval (CI) 0.52-0.66] and 80.2% (kappa=0.6, 95% CI 0.55-0.68) between the HC2 and PANArray HPV tests. Among the 62 patients negative on PANArray HPV (defined as the absence of high risk HPV), but positive on both cobas 4800 HPV and HC2 tests, 42 (67.7%) tested positive for HPV-other' types on the PANArray I I PV test, and 31(50.0%) had gray zone results [relative light unit/control (RLU/CO), 1.4-9.25] in the HC2 test Of the patients deemed positive by the PANArray HPV test, 43 tested positive for high-risk (HR) HPV in cobas 4800 HPV and HC 2 tests. Among them, 58.2% showed HR HPV, including HPV 16, by direct sequencing, of which 25% had gray results. Conclusion: Results classified as 'HPV-other' type by the PANArray HPV test, or gray one results by HC2 (RLU/CO ratio level 1-10) should be carefully interpreted using comprehensive clinical information.
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Human papilloma virus (HPV),atypical squamous cells of undetermined significance (ASCUS),HPV test,concordance