Multi-center evaluation of the Alinity m HR HPV assay with liquid-based cytology cervical specimens in the United States.

IF 3.8 2区 生物学 Q2 MICROBIOLOGY Microbiology spectrum Pub Date : 2025-03-04 Epub Date: 2025-01-27 DOI:10.1128/spectrum.01918-24
D Yitzchak Goldstein, Tong Yang, Danijela Lucic, Yan Zhang, Richard Cullum, Joshua Kostera, Anami Patel
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Abstract

Incorporating molecular testing for human papillomavirus (HPV) into the screening of cervical specimens can improve risk stratification and, in turn, patient management. Infection with a high-risk (HR) HPV genotype is associated with greater risk for persistent infection, viral integration, and progression of cervical neoplasia. Current guidelines consider HPV 16 or HPV 18 clinically actionable with referral to colposcopy; however, 12 Other HR HPV genotypes have been associated with cervical cancer risk, suggesting a benefit of extended genotyping. In this multi-center study, we evaluated the performance of the Alinity m HR HPV assay, which reports HPV 16, 18, and 45 individually and aggregates of HPV 31/33/52/58 and HPV 35/39/51/56/59/66, compared with cobas HPV and Aptima HPV assays, across a variety of cytology result categories. A total of 746 de-identified residual cervical specimens, collected as part of routine cervical cancer screening programs, were tested using Alinity m HR HPV and at least one comparator assay. The overall percent agreement was ≥90.7% for results from the Alinity m HR HPV assay and cobas HPV assays and 90.5% for results from the Alinity m HR HPV and Aptima HPV assay. In patients with any abnormal cytology result, Alinity m identified 78 specimens with non-HPV 16/18 results, underscoring the benefit of detecting additional HR HPV genotypes to guide patient management more accurately. Among specimens with normal cytology, Alinity m detected 14 additional specimens with non-HPV 16/18 genotypes. Extended HR HPV testing can provide additional information to triage patients for appropriate testing and follow-up.IMPORTANCEExtended genotyping for high-risk human papillomavirus (HPV) types enhances diagnostic precision by identifying additional oncogenic HPV types beyond 16 and 18 therefore offering a more nuanced risk profile. This more comprehensive detection may aid in identifying persistent infections that are more likely to progress, thereby supporting future risk-based patient management strategies.

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多中心评价Alinity m HR HPV检测液基细胞学宫颈标本在美国。
将人乳头瘤病毒(HPV)分子检测纳入宫颈标本筛查可以改善风险分层,进而改善患者管理。高危(HR) HPV基因型感染与持续感染、病毒整合和宫颈肿瘤进展的风险增加有关。目前的指南认为HPV 16或HPV 18在临床上是可采取阴道镜检查的;然而,其他12种HR HPV基因型与宫颈癌风险相关,这表明扩展基因分型是有益的。在这项多中心研究中,我们评估了Alinity m HR HPV检测的性能,与cobas HPV和Aptima HPV检测相比,Alinity m HR HPV检测分别报告了HPV 16、18和45,以及HPV 31/33/52/58和HPV 35/39/51/56/59/66的聚集,涵盖了各种细胞学结果类别。作为常规宫颈癌筛查计划的一部分,共收集了746例未鉴定的残留宫颈标本,使用Alinity m HR HPV和至少一种比较物试验进行了检测。Alinity m HR HPV检测和cobas HPV检测结果的总体一致性百分比≥90.7%,Alinity m HR HPV检测和Aptima HPV检测结果的总体一致性百分比为90.5%。在任何细胞学结果异常的患者中,Alinity m发现了78例非HPV 16/18结果的标本,强调了检测额外的HR HPV基因型以更准确地指导患者管理的益处。在细胞学正常的标本中,Alinity m检测到另外14例非hpv 16/18基因型标本。扩展的人乳头瘤病毒检测可以提供额外的信息,以分类患者进行适当的检测和随访。重要性:对高危型人乳头瘤病毒(HPV)的扩展基因分型通过识别16和18岁以上的其他致癌型HPV提高了诊断精度,因此提供了更细致的风险概况。这种更全面的检测可能有助于识别更有可能进展的持续性感染,从而支持未来基于风险的患者管理策略。
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来源期刊
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
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