首页> 外文期刊>International Journal of Cancer =: Journal International du Cancer >Long-term HPV type-specific risks of high-grade cervical intraepithelial lesions: A 14-year follow-up of a randomized primary HPV screening trial
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Long-term HPV type-specific risks of high-grade cervical intraepithelial lesions: A 14-year follow-up of a randomized primary HPV screening trial

机译:高级别宫颈上皮内病变的长期HPV类型特异性风险:一项随机原发性HPV筛查试验的14年随访

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摘要

Quantitative knowledge of the long-term human papillomavirus (HPV) type-specific risks for high-grade cervical intraepithelial neoplasias Grades 2 and 3 (CIN2 and CIN3) is useful for estimating the effect of elimination of specific HPV types and clinical benefits of screening for specific HPV types. We estimated HPV type-specific risks for CIN2 and CIN3 using a randomized primary HPV screening trial followed up for 14.6 years using comprehensive, nationwide registers. Poisson regression estimated cumulative incidences, population attributable proportions (PAR) and incidence rate ratios (IRRs) of high-grade lesions by baseline HPV type, with censoring at date of first CIN2/3 or last registered cytology. Multivariate analysis adjusted for coinfections. IRRs were highest during the first screening round, but continued to be high throughout follow-up (IRRs for CIN3 associated with high-risk (HR) HPV positivity were 226.9, 49.3, 17.7 and 10.3 during the first, second and third screening round and for >9 years of follow-up, respectively). Increased long-term risks were found particularly for HPV Types 16, 18 and 31 and for CIN3+ risks. HPV16/18/31/33 had 14-year cumulative incidences for CIN3+ above 28%, HPV35/45/52/58 had 14 year risks between 14% and 18% and HPV39/51/56/59/66/68 had risks <10%. HPV16 contributed to the greatest proportion of CIN2+ (first round PAR 36%), followed by Types 31, 52, 45 and 58 (7-11%). HPV16/18/31/33/45/52/58 together contributed 73.9% of CIN2+ lesions and all HR types contributed 86.9%. In summary, we found substantial differences in risks for CIN2 and CIN3 between different oncogenic HPV types. These differences may be relevant for both clinical management and design of preventive strategies.
机译:对2级和3级高级别宫颈上皮内瘤变(CIN2和CIN3)的长期人类乳头瘤病毒(HPV)类型特异性风险的定量知识可用于评估消除特定HPV类型的效果以及筛查HPV的临床益处特定的HPV类型。我们使用一项随机的,初步的HPV筛查试验,通过使用全国范围内全面的登记册进行了14.6年的随访,估计了CIN2和CIN3的HPV类型特异性风险。 Poisson回归通过基线HPV类型估计了高级别病变的累积发生率,人群归因比例(PAR)和发生率比率(IRR),并在首次CIN2 / 3或最后一次细胞学检查时进行了检查。多变量分析针对合并感染进行了调整。 IRR在第一轮筛选中最高,但在整个随访期间仍很高(在第一轮,第二轮和第三轮筛选中,与高风险(HR)HPV阳性相关的CIN3的IRR为226.9、49.3、17.7和10.3。分别进行了9年以上的随访)。发现长期风险增加,尤其是对于16型,18型和31型HPV和CIN3 +风险。 HPV16 / 18/31/33具有14年的CIN3 +累积发病率超过28%,HPV35 / 45/52/58具有14年和18%之间的14年风险,HPV39 / 51/56/59/66/68具有风险<10%。 HPV16对CIN2 +的贡献最大(第一轮PAR为36%),其次为Type 31、52、45和58(7-11%)。 HPV16 / 18/31/33/45/52/58共同贡献了73.9%的CIN2 +病变,所有HR类型贡献了86.9%。总而言之,我们发现不同致癌型HPV之间CIN2和CIN3的风险存在实质性差异。这些差异可能与临床管理和预防策略的设计有关。

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