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