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西班牙宫颈癌筛查中配对的自我采集与临床医生采集样本的高危型人乳头瘤病毒检测结果一致性

Agreement Between High-Risk Human Papillomavirus Testing in Paired Self-Collected and Clinician-Collected Samples from Cervical Cancer Screening in Spain.

作者信息

Ibáñez Raquel, Roura Esther, Morey Francisca, Andújar Miguel, Pavón Miquel Ángel, Acera Amelia, Bruni Laia, de Sanjosé Silvia

机构信息

Cancer Epidemiology Research Programme, Catalan Institute of Oncology-Bellvitge Biomedical Research Institute (IDIBELL), L'Hospitalet de Llobregat, 08908 Barcelona, Spain.

Centro de Investigación Biomédica en Red de Epidemiología y Salud Pública (CIBERESP), 28029 Madrid, Spain.

出版信息

Cancers (Basel). 2024 Dec 29;17(1):63. doi: 10.3390/cancers17010063.

Abstract

: Implementing self-sampling (SS) in cervical cancer screening requires comparable results to clinician-collected samples (CCS). Agreement measures are essential for evaluating HPV test performance. Previous studies on non-paired samples have reported higher viral cycle threshold (Ct) values in SS compared to CCS, affecting sensitivity for detecting cervical intraepithelial neoplasia grade 2 or worse (CIN2+). We aimed to evaluate the agreement of high-risk (hr)HPV testing results between SS and CCS using paired samples and to explore differences in Ct values. : Women aged 30 to 65 years attending cervical cancer screening in two regions of Spain were invited to participated in this study. For each woman there was: CCS collected during the screening visit using liquid-based cytology and cytobrush, and a SS using a brush at home one month later. A PCR-based assay was used for hrHPV detection. Agreement in hrHPV results among both samples, Ct value differences, and their association with screening outcomes were analyzed. : This study included 981 women with paired samples. SS had a higher hrHPV prevalence than CCS (overall ratio of 1.3). Positive agreement for all hrHPV genotypes, HPV16, HPV18, and other hrHPV types were 85%, 91.3%, 66.7%, and 83.3%, respectively. Negative agreement was >95% for all results. Median Ct values was slightly higher in SS than in CSS (32.9 vs. 30.6, = 0.02). Seven CIN2+ cases HPV positive were detected by both methods. One CIN3 case was missed by SS. : This study showed a good agreement between SS and CCS for hrHPV testing in a routine screening in Spain. Despite the slightly higher Ct values for SS, no significant impact on sensitivity could be determined due to the low incidence of CIN2+ cases. Further research on larger paired samples is needed to assess the implications of Ct values on test sensitivity.

摘要

在宫颈癌筛查中实施自我采样(SS)需要与临床医生采集的样本(CCS)取得可比的结果。一致性测量对于评估人乳头瘤病毒(HPV)检测性能至关重要。以往对非配对样本的研究报告称,与CCS相比,SS中的病毒循环阈值(Ct)值更高,这影响了检测宫颈上皮内瘤变2级或更严重病变(CIN2+)的敏感性。我们旨在使用配对样本评估SS和CCS之间高危(hr)HPV检测结果的一致性,并探讨Ct值的差异。:邀请西班牙两个地区参加宫颈癌筛查的30至65岁女性参与本研究。对于每位女性,有:在筛查就诊期间使用液基细胞学和细胞刷采集的CCS,以及一个月后在家中使用刷子进行的SS。采用基于聚合酶链反应(PCR)的检测方法进行hrHPV检测。分析了两个样本之间hrHPV结果的一致性、Ct值差异及其与筛查结果的关联。:本研究纳入了981名有配对样本的女性。SS的hrHPV患病率高于CCS(总体比率为1.3)。所有hrHPV基因型、HPV16、HPV18和其他hrHPV类型的阳性一致性分别为85%、91.3%、66.7%和83.3%。所有结果的阴性一致性均>95%。SS中的Ct值中位数略高于CSS(32.9对30.6,P = 0.02)。两种方法均检测到7例HPV阳性的CIN2+病例。SS漏检了1例CIN3病例。:本研究表明,在西班牙的常规筛查中,SS和CCS在hrHPV检测方面具有良好的一致性。尽管SS的Ct值略高,但由于CIN2+病例的低发病率,无法确定对敏感性有显著影响。需要对更大的配对样本进行进一步研究,以评估Ct值对检测敏感性的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d63/11718957/14e4d15857d7/cancers-17-00063-g001.jpg

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