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高级别宫颈上皮内瘤变的临床进展:从双 censored 国家登记数据估算临床前宫颈癌的时间。

Clinical progression of high-grade cervical intraepithelial neoplasia: estimating the time to preclinical cervical cancer from doubly censored national registry data.

出版信息

Am J Epidemiol. 2013 Oct 1;178(7):1161-9. doi: 10.1093/aje/kwt077. Epub 2013 Jul 28.

DOI:10.1093/aje/kwt077
PMID:23897645
Abstract

Little is known about the time span of progression from high-grade cervical intraepithelial neoplasia (CIN2/3) to invasive cervical cancer. Estimation of this duration from longitudinal studies is not permitted, as CIN2/3 should be treated when detected. Cross-sectional data on the age-specific incidence of detected CIN2/3 and cervical cancer cases are readily available in national registries, but these data are difficult to interpret because neither the moment of lesion development nor the onset of invasive cancer is observed. We developed a statistical model for estimating the duration of time between CIN2/3 and preclinical cancer using Dutch national registries for the years 2000-2005. Human papillomavirus (HPV) genotype data were used to separate CIN2/3 and cancer incidences to obtain estimates for HPV-16-positive and HPV-16-negative lesions. The median time from CIN2/3 to cancer was estimated to be 23.5 years (95% confidence interval: 20.8, 26.6), and 1.6% of the lesions progressed to cancer within 10 years. The median duration for HPV-16-positive lesions was similar, but 2.4% of the HPV-16-positive lesions progressed to cancer within 10 years, as compared with 0.6% for HPV-16-negative lesions. Estimated durations of time to cancer are essential for reassessment of the optimal screening interval in light of vaccination and novel screening tests.

摘要

目前对于高级别宫颈上皮内瘤变(CIN2/3)进展为浸润性宫颈癌的时间跨度知之甚少。由于 CIN2/3 一经发现就应进行治疗,因此无法通过纵向研究来估计这段时间。国家登记处有关于特定年龄段已发现的 CIN2/3 和宫颈癌病例的年龄特异性发病率的横断面数据,但这些数据难以解释,因为既无法观察到病变发展的时刻,也无法观察到浸润性癌的发生。我们使用荷兰国家登记处 2000-2005 年的数据,开发了一种用于估计从 CIN2/3 到临床前癌症的时间跨度的统计模型。使用人乳头瘤病毒(HPV)基因型数据将 CIN2/3 和癌症发病率分开,以获得 HPV-16 阳性和 HPV-16 阴性病变的估计值。从 CIN2/3 到癌症的中位时间估计为 23.5 年(95%置信区间:20.8,26.6),10 年内有 1.6%的病变进展为癌症。HPV-16 阳性病变的中位持续时间相似,但在 10 年内,2.4%的 HPV-16 阳性病变进展为癌症,而 HPV-16 阴性病变为 0.6%。癌症发生的时间估计对于根据疫苗接种和新型筛查试验重新评估最佳筛查间隔至关重要。

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