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二价型人乳头瘤病毒疫苗补种对宫颈癌筛查结果的影响:来自英国 HPV 初级筛查试验的观察性研究。

The impact of catch-up bivalent human papillomavirus vaccination on cervical screening outcomes: an observational study from the English HPV primary screening pilot.

机构信息

Cancer Prevention Group, School of Cancer & Pharmaceutical Sciences, Faculty of Life Sciences & Medicine, King's College London, Great Maze Pond, London, SE1 9RT, UK.

Cancer Prevention Trials Unit, School of Cancer & Pharmaceutical Sciences, Faculty of Life Sciences & Medicine, King's College London, Great Maze Pond, London, SE1 9RT, UK.

出版信息

Br J Cancer. 2022 Jul;127(2):278-287. doi: 10.1038/s41416-022-01791-w. Epub 2022 Mar 26.

DOI:10.1038/s41416-022-01791-w
PMID:35347326
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9296648/
Abstract

BACKGROUND

In England, bivalent vaccination (Cervarix) against high-risk human papillomavirus (HR-HPV) genotypes 16/18 was offered in a population-based catch-up campaign in 2008-2010 to girls aged 14-17 years. These women are now entering the national cervical screening programme. We determined the impact of catch-up bivalent vaccination on their screening outcomes.

METHODS

We studied the overall and genotype-specific screening outcomes in 108,138 women aged 24-25 (offered vaccination) and 26-29 years (not offered vaccination) included in the English HPV screening pilot between 2013 and 2018.

RESULTS

At 24-25 years, the detection of high-grade cervical intraepithelial neoplasia (CIN2+) associated with HPV16/18 decreased from 3 to 1% (p < 0.001), with estimated vaccine effectiveness of 87% (95% CI: 82-91%). The detection of any CIN2+ halved from 6 to 3% (p < 0.001), with an estimated vaccine effectiveness of 72% (95% CI: 66-77%). The positive predictive value of a colposcopy for CIN2+ decreased for both low-grade (p < 0.001) and high-grade (p = 0.02) abnormalities on triage cytology. The decreases in screen-detected abnormalities at age 26-29 were of a substantially smaller magnitude.

CONCLUSIONS

These data confirm high effectiveness of bivalent HPV vaccination delivered through a population-based catch-up campaign in England. These findings add to the rationale for extending screening intervals for vaccinated cohorts.

摘要

背景

2008-2010 年,在英国,针对高危型人乳头瘤病毒(HR-HPV)基因型 16/18 的二价疫苗(Cervarix)在一项基于人群的补种活动中提供给 14-17 岁的女孩。这些女性现在正在进入国家宫颈癌筛查计划。我们确定了补种二价 HPV 疫苗对她们筛查结果的影响。

方法

我们研究了 2013 年至 2018 年间参加英国 HPV 筛查试验的 108138 名 24-25 岁(接种疫苗)和 26-29 岁(未接种疫苗)女性的总体和基因型特异性筛查结果。

结果

在 24-25 岁时,与 HPV16/18 相关的高级别宫颈上皮内瘤变(CIN2+)的检出率从 3%降至 1%(p<0.001),疫苗有效性估计为 87%(95%CI:82-91%)。任何 CIN2+的检出率从 6%降至 3%(p<0.001),疫苗有效性估计为 72%(95%CI:66-77%)。阴道镜检查对细胞学分流中低度(p<0.001)和高度(p=0.02)异常的 CIN2+的阳性预测值降低。在 26-29 岁时,筛查发现的异常情况的减少幅度要小得多。

结论

这些数据证实了在英国通过基于人群的补种活动提供的二价 HPV 疫苗具有很高的有效性。这些发现为延长接种疫苗队列的筛查间隔提供了更多的依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4312/9296648/a66a700037c0/41416_2022_1791_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4312/9296648/7c50a1f50089/41416_2022_1791_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4312/9296648/70b8f356a600/41416_2022_1791_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4312/9296648/1c57f1ce3f18/41416_2022_1791_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4312/9296648/6a541e67f000/41416_2022_1791_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4312/9296648/a66a700037c0/41416_2022_1791_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4312/9296648/7c50a1f50089/41416_2022_1791_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4312/9296648/70b8f356a600/41416_2022_1791_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4312/9296648/1c57f1ce3f18/41416_2022_1791_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4312/9296648/6a541e67f000/41416_2022_1791_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4312/9296648/a66a700037c0/41416_2022_1791_Fig5_HTML.jpg

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