在芬兰宫癌查计划中,高风险的人类乳头瘤病毒与细胞学查两轮:基于人口的队列研究
Iiris Juulia Turunen1,2, Ilkka Kalliala1,3, Maiju Pankakoski2
1Department of Obstetrics and Gynaecology, Helsinki University Hospital, Helsinki, Finland.
BMJ medicine
|October 10, 2025
概括
高风险人乳头瘤病毒 (hrHPV) 查比细胞学查更有效,可以更早地检测宫癌前病变. hrHPV查是安全有效的,在特定子组中可能需要更长的查间隔.
科学领域:
- 妇科瘤学 妇科瘤学
- 公共卫生 公共卫生
- 查计划 查计划
背景情况:
- 子宫癌查计划旨在早期检测癌前病变.
- 细胞学查 (巴氏涂抹) 是标准的,但高危人乳头瘤病毒 (hrHPV) 测试提供了潜在的改善.
- 在例行计划中比较hrHPV和细胞学查对于优化宫癌预防至关重要.
研究的目的:
- 为了比较常规高风险人类乳头瘤病毒 (hrHPV) 查与细胞学查在宫癌预防中的有效性.
- 评估2级或更高 (CIN2+) 的宫内皮质瘤的检测率和两轮查中的结肠镜转诊率.
- 评估hrHPV查的安全性和有效性,在一个成熟的国家查计划中进行查.
主要方法:
- 基于人口的队列研究使用芬兰大规模查注册表 (2012-2022) 的数据进行.
- 1,180,491名妇女参加了细胞学或基于HRHPV的宫癌查.
- 结果包括出席率,阳性测试结果,肠镜转诊和因人口因素而调整后的CIN2+发病率.
主要成果:
- 与细胞学查 (0.98%和0.35%分别) 相比,hrHPV查导致显著更高的肠镜转诊率 (3.37%) 和CIN2+检测率 (0.92%) .
- 与第一轮 (3.54%和0.98%) 相比,第二轮 hrHPV 查显示了转诊率 (2.42%) 和 CIN2+ 检测率 (0.38%) 的降低.
- 细胞学查没有显示转诊或CIN2+发现在轮次之间减少. 在第一轮的负 hrHPV 测试与第二轮的 CIN2+ 风险非常低 (0.2%).
结论:
- 常规的hrHPV查是有效和安全的,比细胞学查更早地识别癌前病变.
- 该研究表明,每隔五年对 hrHPV 的查间隔是适当的.
- 对于特定的子组,可以考虑较长的查间隔,例如具有负 hrHPV 测试的女性或50岁及以上的女性,以优化资源配置和患者管理.
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