University Research Clinic for Cancer Screening, Department of Public Health Programmes, Randers Regional Hospital, Randers, Denmark.
Department of Obstetrics and Gynecology, Odense University Hospital, Odense, Denmark.
PLoS Med. 2023 Jul 6;20(7):e1004253. doi: 10.1371/journal.pmed.1004253. eCollection 2023 Jul.
High-risk human papillomavirus (HPV) test is replacing cytology as the primary cervical cancer screening test due to superior sensitivity, but in most countries women ≥65 years have never had an HPV test despite they account for around 50% of cervical cancer deaths. We explored the effect of a catch-up HPV test among 65- to 69-year-old women without previous record of HPV-based screening.
This population-based nonrandomized intervention study (quasi-experimental design) included Danish women aged 65 to 69 with no record of cervical cancer screening in the last ≥5.5 years and no HPV-exit test at age 60 to 64 at the time of study inclusion. Eligible women residing in the Central Denmark Region were invited for HPV screening either by attending clinician-based sampling or requesting a vaginal self-sampling kit (intervention group, n = 11,192). Women residing in the remaining four Danish regions received standard care which was the opportunity to have a cervical cytology collected for whatever reason (reference group, n = 33,387). Main outcome measures were detection of cervical intraepithelial neoplasia (CIN) grade 2 or worse (CIN2+) per 1,000 women eligible for the screening offer and the benefit-harm ratio of the intervention and standard practice measured as the number of colposcopies needed to detect one CIN2+ case. The minimum follow-up time was 13 months for all tested women (range: 13 to 25 months). In the intervention group, 6,965 (62.2%) were screened within 12 months from the date of study inclusion and 743 (2.2%) women had a cervical cytology collected in the reference group. The CIN2+ detection was significantly higher in the intervention group (3.9, 95% confidence interval (CI): [2.9, 5.3]; p < 0.001; n = 44/11,192) as compared to the reference group (0.3, 95% CI: [0.2, 0.6]; n = 11/33,387). For the benefit-harm ratio, 11.6 (95% CI: [8.5, 15.8]; p = 0.69; n = 511/44) colposcopies were performed to detect one CIN2+ in the intervention group as compared to 10.1 (95% CI: [5.4, 18.8]; n = 111/11) colposcopies in the reference group. The study design entails a risk of confounding due to the lack of randomization.
The higher CIN2+ detection per 1,000 eligible women in the intervention group supports that a catch-up HPV test could potentially improve cervical cancer prevention in older women. This study informs the current scientific debate as to whether women aged 65 and above should be offered a catch-up HPV test if they never had an HPV test.
ClinicalTrials.gov NCT04114968.
由于高灵敏度,高危型人乳头瘤病毒(HPV)检测正取代细胞学成为宫颈癌筛查的主要方法,但在大多数国家,≥65 岁的女性从未接受过 HPV 检测,尽管她们约占宫颈癌死亡人数的 50%。我们研究了对 65-69 岁、既往无 HPV 筛查记录且 60-64 岁时无 HPV 退出检测的女性进行 HPV 追赶检测的效果。
这是一项基于人群的非随机干预研究(准实验设计),纳入了丹麦年龄在 65-69 岁之间、过去≥5.5 年无宫颈癌筛查记录且在研究纳入时 60-64 岁时无 HPV 退出检测的女性。居住在丹麦中部地区的符合条件的女性通过就诊时的医生采样或要求阴道自我采样套件接受 HPV 筛查(干预组,n=11192)。居住在丹麦其他四个地区的女性接受标准护理,即有机会出于任何原因采集宫颈细胞学样本(对照组,n=33387)。主要结局测量为每 1000 名有筛查机会的女性中检测到的宫颈上皮内瘤变(CIN)2 级或更高级别(CIN2+)的数量,以及干预和标准实践的获益-危害比,以发现一个 CIN2+病例所需的阴道镜检查数量来衡量。所有接受检测的女性的最低随访时间为 13 个月(范围:13-25 个月)。在干预组中,6965 名(62.2%)女性在研究纳入日期后 12 个月内接受了筛查,743 名(2.2%)女性在对照组中采集了宫颈细胞学样本。与对照组(0.3,95%置信区间[0.2,0.6];n=11/33387)相比,干预组的 CIN2+检出率显著更高(3.9,95%置信区间[2.9,5.3];p<0.001;n=44/11192)。对于获益-危害比,干预组为发现一个 CIN2+需要进行 11.6 次阴道镜检查(95%置信区间[8.5,15.8];p=0.69;n=511/44),而对照组为 10.1 次(95%置信区间[5.4,18.8];n=111/11)。由于缺乏随机化,研究设计存在混杂的风险。
干预组每 1000 名有筛查机会的女性中 CIN2+的检出率更高,这支持了对老年女性进行 HPV 追赶检测可能有助于改善宫颈癌预防。本研究为当前关于是否应向 65 岁及以上的女性提供 HPV 追赶检测的科学辩论提供了信息,如果她们从未接受过 HPV 检测。
ClinicalTrials.gov NCT04114968。