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在瑞典有组织的宫颈癌筛查项目中,为长期未参与者自行采集阴道HPV样本。

Self-collected vaginal HPV samples for long-term non-attendees in the Swedish organized cervical cancer screening program.

作者信息

Sundqvist Avalon, Hellsten Caroline, Strander Björn, Lindh Magnus, Borgfeldt Christer

机构信息

Department of Obstetrics and Gynecology, Skåne University Hospital and Lund University, Lund, Sweden.

Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.

出版信息

Acta Obstet Gynecol Scand. 2025 Jun;104(6):1181-1189. doi: 10.1111/aogs.15112. Epub 2025 Apr 7.

Abstract

INTRODUCTION

Most cervical cancer cases in Sweden are diagnosed among women who have failed to attend screening. The objective of this study was to analyze the effectiveness of offering vaginal HPV (human papillomavirus) self-samples to long-term non-attendees as a routine in this screening program, in which non-attendees had already been the targets of several interventions.

MATERIAL AND METHODS

Register data from the organized cervical screening program were used in this population-based study. From January 2016 to December 2019, 33 881 high-risk (hr-) HPV self-sample kits were sent to the homes of long-term screening non-attendees (≥7 years without a registered screening test), aged between 29 and 64 years, in Region Västra Götaland, Sweden. All samples returned to the laboratory were analyzed with the Cobas HPV DNA assay (Roche) for HPV16, HPV18, and for 12 other hr-HPV types. HPV-positive women were referred for colposcopy. Compliance and results of follow-up were assessed 12 months after HPV analysis. Descriptive statistics, trend analysis, and risk ratios were used to compare outcomes across groups.

RESULTS

The median age of invited women was 49 years; 35% had not been screened before. The response rate was 19.4% (6582/33881). The HPV prevalence was 12.0% (788/6582), and 80.2% of HPV-positive women attended follow-up. Women with no previous cervical sample had a lower response rate: 15.7% (RR (Risk ratio) 0.73 (95% CI (Confidence interval) 0.70-0.77)). They also had lower attendance in follow-up when HPV-positive (71.6% RR 0.86 (CI 0.78-0.94)), compared with women who had previous samples. The proportions of high-grade histopathology (HSIL+) among followed-up women were 31.3% for HPV16, 15.2% for HPV18, and 8.8% for HPVnon-16/18. Nine cervical cancer cases were found among 6582 women, corresponding to a rate of 137 cases per 100,000 women.

CONCLUSIONS

Vaginal HPV self-samples increased cervical screening attendance by almost one-fifth among non-attendees who had previously resisted several invitations and interventions. Biopsied women positive for HPV16 or HPV18 had a high prevalence of HSIL or cervical cancer, which strongly supports direct referral to colposcopy. Long-term non-attendees have an exceptionally high risk of cervical cancer and should receive special attention.

摘要

引言

瑞典大多数宫颈癌病例是在未参加筛查的女性中被诊断出来的。本研究的目的是分析在该筛查项目中,向长期未参加者提供阴道人乳头瘤病毒(HPV)自我采样作为常规操作的有效性,在这个筛查项目中,未参加者已经是多项干预措施的目标人群。

材料与方法

在这项基于人群的研究中,使用了来自有组织的宫颈癌筛查项目的登记数据。2016年1月至2019年12月期间,33881份高危(hr-)HPV自我采样试剂盒被送到瑞典韦斯特罗斯地区29至64岁的长期筛查未参加者(≥7年无登记筛查检测)家中。所有返回实验室的样本都采用Cobas HPV DNA检测法(罗氏公司)对HPV16、HPV18以及其他12种hr-HPV类型进行检测。HPV阳性的女性被转诊进行阴道镜检查。在HPV分析12个月后评估依从性和随访结果。使用描述性统计、趋势分析和风险比来比较各组的结果。

结果

受邀女性的中位年龄为49岁;35%的女性之前未接受过筛查。响应率为19.4%(6582/33881)。HPV感染率为12.0%(788/6582),80.2%的HPV阳性女性参加了随访。之前没有宫颈样本的女性响应率较低:为15.7%(风险比(RR)0.73(95%置信区间(CI)0.70 - 0.77))。与有过样本的女性相比,她们在HPV阳性时的随访参与率也较低(71.6%,RR 0.86(CI 0.78 - 0.94))。在接受随访的女性中,HPV16的高级别组织病理学(HSIL+)比例为31.3%,HPV18为15.2%,非HPV16/18为8.8%。在6582名女性中发现了9例宫颈癌病例,相当于每10万名女性中有137例。

结论

阴道HPV自我采样使之前拒绝多次邀请和干预的未参加者的宫颈癌筛查参与率提高了近五分之一。HPV16或HPV18检测呈阳性且接受活检的女性中,HSIL或宫颈癌的患病率很高,这有力地支持了直接转诊进行阴道镜检查。长期未参加者患宫颈癌的风险极高,应给予特别关注。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7d0/12087532/a834e53af969/AOGS-104-1181-g004.jpg

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