Affiliations of authors: Virus, Lifestyle and Genes (BB-F, CM, SKK) and Statistics, Bioinformatics and Registry (CD), Danish Cancer Society Research Center, Copenhagen, Denmark; Gynaecological Clinic, Juliane Marie Centre, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark (SKK).
J Natl Cancer Inst. 2014 Mar;106(3):djt460. doi: 10.1093/jnci/djt460. Epub 2014 Feb 19.
In clinical trials, vaccines against human papillomavirus (HPV) have been highly effective against HPV16- or HPV18-associated cervical lesions. The quadrivalent HPV vaccine was licensed in 2006 and subsequently implemented in the Danish vaccination program. The study aim was to use individual information on HPV vaccination status to assess subsequent risk of cervical lesions.
Using a cohort study design, we identified all girls and women born in Denmark in the period from 1989 to 1999 and obtained information on individual HPV vaccination status in the period from 2006 to 2012 from nationwide registries. Incident cases of cervical lesions were identified by linkage to the nationwide Pathology Data Bank. We compared vaccinated and unvaccinated girls and women stratified by birth cohort in Cox proportional hazards models.
Risk of atypia or worse (atypia+) and of cervical intraepithelial neoplasia grade 2 or 3 (CIN2/3) were statistically significantly reduced among vaccinated women in birth cohorts 1991 to 1994 (1991-1992atypia+: hazard ratio [HR] = 0.46, two-sided 95% confidence interval [CI] = 0.39 to 0.56; 1991-1992CIN2/3: HR = 0.56, 95% CI = 0.37 to 0.84; 1993-1994atypia+: HR = 0.40, 95% CI = 0.29 to 0.56; 1993-1994 CIN2/3: HR = 0.27, 95% CI = 0.10 to 0.67). The birth cohort 1989 to 1990 had a statistically significantly reduced risk of atypia+ (HR = 0.75; 95% CI = 0.65 to 0.86); the risk of CIN2/3 was also decreased but not statistically significant. No events occurred among girls in the birth cohort 1997 to 1999, whereas for the birth cohort 1995 to 1996 a hazard ratio could be calculated only for atypia+.
Six years after licensure of the quadrivalent HPV vaccine in Denmark, a reduced risk of cervical lesions is observed at the population level.
在临床试验中,针对人乳头瘤病毒(HPV)的疫苗对 HPV16 或 HPV18 相关的宫颈病变具有高度有效性。四价 HPV 疫苗于 2006 年获得许可,并随后在丹麦接种计划中实施。本研究的目的是利用 HPV 接种状态的个体信息来评估宫颈病变的后续风险。
我们使用队列研究设计,确定了 1989 年至 1999 年期间在丹麦出生的所有女孩和妇女,并从全国性登记处获得了 2006 年至 2012 年期间 HPV 接种状态的个体信息。通过与全国性病理学数据库的链接,确定了宫颈病变的发病病例。我们将接种疫苗和未接种疫苗的女孩和妇女按出生队列分层,并在 Cox 比例风险模型中进行比较。
在 1991 年至 1994 年出生队列中,接种疫苗的女性发生异常或更严重病变(异常+)和宫颈上皮内瘤变 2 级或 3 级(CIN2/3)的风险统计学上显著降低(1991-1992 年异常+:风险比[HR] = 0.46,双侧 95%置信区间[CI] = 0.39 至 0.56;1991-1992 年 CIN2/3:HR = 0.56,95%CI = 0.37 至 0.84;1993-1994 年异常+:HR = 0.40,95%CI = 0.29 至 0.56;1993-1994 年 CIN2/3:HR = 0.27,95%CI = 0.10 至 0.67)。1989 年至 1990 年出生队列的异常+风险统计学上显著降低(HR = 0.75;95%CI = 0.65 至 0.86);CIN2/3 的风险也降低了,但无统计学意义。1997 年至 1999 年出生的女孩中未发生任何事件,而对于 1995 年至 1996 年出生的女孩,只能计算异常+的风险比。
在丹麦四价 HPV 疫苗获得许可六年后,在人群水平上观察到宫颈病变风险降低。