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在常规实践中通过高危型 HPV 检测进行宫颈癌筛查:高危型 HPV 阳性和细胞学阴性女性一年随访的结果。

Cervical cancer screening by high risk HPV testing in routine practice: results at one year recall of high risk HPV-positive and cytology-negative women.

机构信息

Immunology and Molecular Oncology Unit, Veneto Oncology Institute IOV IRCCS, Padova, Italy.

出版信息

J Med Screen. 2014 Mar;21(1):30-7. doi: 10.1177/0969141314522219. Epub 2014 Jan 31.

Abstract

OBJECTIVE

Cervical cancer screening by human papillomavirus (HPV) testing requires the use of additional triage and follow-up analyses. We evaluated women's compliance with and the performance of this strategy in a routine setting.

SETTING

Five cervical service screening programmes in North-East Italy.

METHODS

Eligible women aged 25-64 invited for a new screening episode underwent HPV testing for high risk types (hrHPV by Hybrid Capture 2) and cytology triage. Women with positive HPV and cytology results were referred for colposcopy; women with positive HPV but negative cytology results were referred to 1-year repeat hrHPV testing.

RESULTS

Of 46,694 women screened by HPV testing up to December 2011, 3,211 (6.9%) tested hrHPV positive; 45% of these had a positive triage cytology. Those with negative cytology were invited for 1-yr repeat testing. Compliance with invitation was 61.6% at baseline and 85.3% at 1-yr repeat. Rate of persistent hrHPV positivity was 58% (830/1,435). Colposcopy performed in women with a positive hrHPV test at 1-yr repeat accounted for 36% of all colposcopies performed within the screening programmes. Cumulatively, a histological high-grade lesion was detected in 276 women (5.9‰ detection rate), 234 at baseline (85%), and 42 (15%) at 1-yr repeat.

CONCLUSIONS

Compliance with hrHPV-based screening programmes was high both at baseline and at 1-yr repeat. Compared with the randomized trials, a higher proportion of triage cytology was read as positive, and only a small number of high-grade lesions were detected among the group of hrHPV positive cytology negative women who repeated testing 1-yr after baseline.

摘要

目的

人乳头瘤病毒(HPV)检测的宫颈癌筛查需要额外的分流和随访分析。我们在常规环境中评估了女性对该策略的依从性及其性能。

地点

意大利东北部的 5 个宫颈服务筛查计划。

方法

邀请新筛查的年龄在 25-64 岁之间的合格女性进行高危型 HPV(杂交捕获 2 型的 HPV)和细胞学分流检测。HPV 和细胞学阳性的女性被转诊行阴道镜检查;HPV 阳性而细胞学阴性的女性被转诊行 1 年重复的高危型 HPV 检测。

结果

截至 2011 年 12 月,对 46694 名接受 HPV 检测的女性进行筛查,其中 3211 名(6.9%)检测出高危型 HPV 阳性;其中 45%的细胞学分流检测呈阳性。细胞学阴性的女性被邀请进行 1 年重复检测。基线时的邀请依从率为 61.6%,1 年重复时的依从率为 85.3%。持续 HPV 阳性的发生率为 58%(830/1435)。在 1 年重复时 HPV 检测阳性的女性中,进行阴道镜检查占筛查计划中所有阴道镜检查的 36%。累计发现 276 名(5.9‰检出率)女性有组织学高级别病变,其中 234 名(85%)在基线时发现,42 名(15%)在 1 年重复时发现。

结论

HPV 检测的宫颈癌筛查的基线和 1 年重复的依从率均较高。与随机试验相比,细胞学分流检测的阳性率更高,并且在基线后 1 年重复检测 HPV 阳性而细胞学阴性的女性中,仅发现少数高级别病变。

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