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<metadata xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/"><dc:title>Clinical evaluation of INNO-LiPA HPV Genotyping EXTRA II assay using the VALGENT framework</dc:title><dc:creator>Xu,	Lan	(Avtor)
	</dc:creator><dc:creator>Padalko,	Elizaveta	(Avtor)
	</dc:creator><dc:creator>Oštrbenk Valenčak,	Anja	(Avtor)
	</dc:creator><dc:creator>Poljak,	Mario	(Avtor)
	</dc:creator><dc:creator>Arbyn,	Marc	(Avtor)
	</dc:creator><dc:subject>INNO-LiPA</dc:subject><dc:subject>VALGENT</dc:subject><dc:subject>HPV genotyping</dc:subject><dc:subject>cervical cancer</dc:subject><dc:subject>human papillomavirus</dc:subject><dc:subject>clinical validation</dc:subject><dc:subject>Hybrid Capture 2</dc:subject><dc:subject>Linear Array</dc:subject><dc:subject>HPV</dc:subject><dc:subject>INNO - LiPA HPV genotyping EXTRA II</dc:subject><dc:description>In this diagnostic test validation study, we assessed the clinical accuracy and HPV genotyping performance of the INNO-LiPA HPV Genotyping Extra II (INNO-LiPA) within the VALGENT-3 framework. VALGENT is designed to assess the analytical and clinical performance of HPV tests with genotyping capacity. The VALGENT-3 panel comprised 1300 consecutive cervical cell specimens enriched with 300 samples with abnormal cytology obtained from women attending the Slovenian cervical cancer screening programme. The INNO-LiPA allows type-specific detection of 32 HPV types; however, for the clinical accuracy assessment, we considered it as high-risk (hr)HPV positive when at least one of the following HPV types was present: HPV16, HPV18, HPV31, HPV33, HPV35, HPV39, HPV45, HPV51, HPV52, HPV56, HPV58, HPV59, and HPV68. Clinical accuracy for detection of cervical intraepithelial neoplasia grade 2 or worse (CIN2+) was compared between INNO-LiPA and Hybrid Capture 2 (HC2), which is a standard comparator test for HPV tests used in cervical cancer screening. In addition, hrHPV and type-specific detection HPV types were compared between INNO-LiPA and Linear Array HPV Genotyping Test (Linear Array). The prevalence of hrHPV determined by INNO-LiPA was 17.1% (95% CI, 15.0–19.2%) in the screening population. HrHPV testing with INNO-LiPA had a sensitivity for CIN2+ of 96.9% (95% CI, 92.1–99.1%) which was non-inferior to HC2 (relative sensitivity of 1.01; 95% CI, 0.97–1.04; p$_{n.inf}$ = 0.0002) and a specificity for ≤CIN1 of 85.3% (95% CI, 83.2–87.3%) which was inferior to HC2 (relative specificity of 0.95; 95% CI, 0.93–0.97; p$_{n.inf}$ = 0.9998). Genotyping agreement between INNO-LiPA and Linear Array was excellent for hrHPV, HPV16, HPV18, HPV35, HPV45, HPV58 and HPV59, but good or fair for other HPV types. To conclude, INNO-LiPA demonstrated non-inferior clinical sensitivity but lower specificity compared to HC2 in addition to excellent concordance compared to Linear Array for hrHPV and some genotypes.</dc:description><dc:date>2018</dc:date><dc:date>2021-09-30 11:48:48</dc:date><dc:type>Članek v reviji</dc:type><dc:identifier>131628</dc:identifier><dc:identifier>ISSN pri članku: 1422-0067</dc:identifier><dc:identifier>DOI: 10.3390/ijms19092704</dc:identifier><dc:identifier>COBISS_ID: 129639683</dc:identifier><dc:language>sl</dc:language></metadata>
