School of Health Sciences, University of Tampere, Tampere 33014, Finland.
Sex Transm Infect. 2011 Aug;87(5):372-6. doi: 10.1136/sti.2010.044354. Epub 2011 Apr 6.
High-risk human papillomavirus (hrHPV) is the primary cause of cervical cancer. As Chlamydia trachomatis is also linked to cervical cancer, its role as a potential co-factor in the development of cervical intraepithelial neoplasia (CIN) grade 2 or higher was examined.
The placebo arms of two large, multinational, clinical trials of an HPV6/11/16/18 vaccine were combined. A total of 8441 healthy women aged 15-26 years underwent cervicovaginal cytology (Papanicolaou (Pap) testing) sampling and C trachomatis testing at day 1 and every 12 months thereafter for up to 4 years. Protocol-specified guidelines were used to triage participants with Pap abnormalities to colposcopy and definitive therapy. The main outcome measured was CIN.
At baseline, 2629 (31.1%) tested positive for hrHPV DNA and 354 (4.2%) tested positive for C trachomatis. Among those with HPV16/18 infection (n = 965; 11.4%) or without HPV16/18 infection (n = 7382, 87.5%), the hazard ratios (HRs) associated with development of any CIN grade 2 according to baseline C trachomatis status were 1.82 (95% CI: 1.06 to 3.14) and 1.74 (95% CI 1.05 to 2.90), respectively. The results were comparable when only the 12 most common hrHPV infections were considered, but the excess risk disappeared when the outcome was expanded to include CIN grade 3 or worse.
Further studies based on larger cohorts with longitudinal follow-up in relation to the C trachomatis acquisition and a thorough evaluation of temporal relationships of infections with hrHPV types, C trachomatis and cervical neoplasia are needed to demonstrate whether and how in some situations C trachomatis sets the stage for cervical carcinogenesis. Trial registration NCT00092521 and NCT00092534.
高危型人乳头瘤病毒(hrHPV)是宫颈癌的主要病因。由于沙眼衣原体也与宫颈癌有关,因此研究了其作为宫颈上皮内瘤变(CIN)2 级或更高级别发展的潜在共同因素的作用。
将两项 HPV6/11/16/18 疫苗大型跨国临床试验的安慰剂组进行了合并。共有 8441 名年龄在 15-26 岁的健康女性在第 1 天和此后的每 12 个月进行宫颈阴道细胞学(巴氏涂片(Pap)检测)采样和 C 型沙眼衣原体检测,最长可达 4 年。根据方案规定的准则,对 Pap 异常的参与者进行阴道镜检查和明确治疗。主要测量的结果是 CIN。
基线时,2629 人(31.1%)HPV DNA 检测呈阳性,354 人(4.2%)C 型沙眼衣原体检测呈阳性。在 HPV16/18 感染者(n = 965;11.4%)或无 HPV16/18 感染者(n = 7382,87.5%)中,根据基线 C 型沙眼衣原体状态,与任何 CIN 2 级发展相关的危险比(HR)分别为 1.82(95%CI:1.06 至 3.14)和 1.74(95%CI 1.05 至 2.90)。当仅考虑 12 种最常见的 hrHPV 感染时,结果相似,但当将结果扩展到包括 CIN 3 级或更高级别时,风险增加消失。
需要基于更大队列进行进一步研究,这些队列需要进行纵向随访以了解 C 型沙眼衣原体的获得情况,并彻底评估 hrHPV 类型、C 型沙眼衣原体和宫颈肿瘤之间感染的时间关系,以证明 C 型沙眼衣原体在某些情况下是否以及如何为宫颈癌的发生奠定基础。试验注册 NCT00092521 和 NCT00092534。