Woman's Health Sciences Department, Gynecologic Section, Polytechnic University of Marche, Ancona, Italy.
Servizio di epidemiologia, Azienda USL-IRCCS di Reggio Emilia, Reggio Emilia, Emilia-Romagna, Italy.
Gynecol Oncol. 2021 Jun;161(3):741-747. doi: 10.1016/j.ygyno.2021.03.025. Epub 2021 Mar 29.
Cervical cancer prevention guidelines include Human Papillomavirus (HPV) test, cytology, and HPV-16/18 typing for triage to determine the risk of cervical intraepithelial neoplasia (CIN) grade 3 as the best proxy of cervical cancer risk. In doing that, they do not consider how age can modify the type-specific risk of CIN3. The present study aimed to evaluate the age-related distribution of HPV genotypes affecting the risk-assessment in cervical cancer screening programs: non-screening-type-HPV and non-HPV-16/18 in unvaccinated women with CIN3.
Retrospective multi-institutional study, including HPV genotyped women with CIN3 on cone histology treated between 2014 and 2019. The sample was divided into three categories of age: <30, 30-44, ≥45. HPV genotypes were grouped in non-screening-type-HPV (not-including genotypes 16/18/31/33/35/39/45/51/52/56/58/59/66/68) and non-HPV-16/18. Associations and trends between different age-groups and HPV genotypes were measured.
1332 women were analyzed. Non-screening-type-HPV CIN3 were 73 (5.5%). Non-HPV-16/18 were found in 417 participants (31.3%). Women over 45 associated with non-screening-type HPV [odds ratio (OR) = 1.87, 95% confidence interval (CI) 1.07-3.25; p = 0.027]. Non-screening-type-HPV prevalence increased significantly with age (3.9% vs 5.1% vs 9.0%, p = 0.016). Women under 30 showed a lower rate of non-HPV-16/18 (OR = 0.65, 95% CI 0.47-0.89; p = 0.007). There was a positive trend with age of non-HPV-16/18 CIN3 (23.6% vs 32.1% vs 38.0%, p = 0.0004).
The proportion of CIN3 lesions unrelated to genotypes detected by primary screening tests increased with age. This implies that age probably modifies the risk of CIN3 and possibly of cancer associated with HPV types. The risk-based recommendation should take into consideration age to define the management of HPV positive women.
宫颈癌预防指南包括人乳头瘤病毒(HPV)检测、细胞学检查和 HPV-16/18 型检测,以进行分流,确定宫颈癌前病变(CIN)3 级的风险,作为宫颈癌风险的最佳替代指标。在这样做的过程中,它们没有考虑年龄如何改变 CIN3 的特定类型风险。本研究旨在评估 HPV 基因型与宫颈癌筛查计划中 CIN3 风险评估相关的年龄分布:未接种疫苗的 CIN3 妇女中的非筛查型 HPV 和非 HPV-16/18。
回顾性多机构研究,包括 2014 年至 2019 年接受锥形组织学治疗的 CIN3 女性的 HPV 基因分型。样本分为 3 个年龄组:<30 岁、30-44 岁和≥45 岁。HPV 基因型分为非筛查型 HPV(不包括基因型 16/18/31/33/35/39/45/51/52/56/58/59/66/68)和非 HPV-16/18。测量不同年龄组与 HPV 基因型之间的关联和趋势。
分析了 1332 名女性。非筛查型 HPV CIN3 为 73 例(5.5%)。417 名参与者发现非 HPV-16/18(31.3%)。45 岁以上的女性与非筛查型 HPV 相关[比值比(OR)=1.87,95%置信区间(CI)1.07-3.25;p=0.027]。非筛查型 HPV 患病率随年龄显著增加(3.9%比 5.1%比 9.0%,p=0.016)。30 岁以下的女性非 HPV-16/18 率较低(OR=0.65,95%CI 0.47-0.89;p=0.007)。非 HPV-16/18 CIN3 年龄呈阳性趋势(23.6%比 32.1%比 38.0%,p=0.0004)。
与初级筛查试验检测到的基因型无关的 CIN3 病变比例随年龄增长而增加。这意味着年龄可能改变 HPV 相关 CIN3 和癌症的风险。基于风险的推荐应考虑年龄,以确定 HPV 阳性女性的管理。