Prevention and Implementation Group, International Agency for Research on Cancer, Lyon, France.
PLoS One. 2013 Jul 17;8(7):e68329. doi: 10.1371/journal.pone.0068329. Print 2013.
Human papillomavirus (HPV) infection, particularly with type 16, causes a growing fraction of oropharyngeal cancers, whose incidence is increasing, mainly in developed countries. In a double-blind controlled trial conducted to investigate vaccine efficacy (VE) of the bivalent HPV 16/18 vaccine against cervical infections and lesions, we estimated VE against prevalent oral HPV infections 4 years after vaccination.
A total of 7,466 women 18-25 years old were randomized (1∶1) to receive the HPV16/18 vaccine or hepatitis A vaccine as control. At the final blinded 4-year study visit, 5,840 participants provided oral specimens (91·9% of eligible women) to evaluate VE against oral infections. Our primary analysis evaluated prevalent oral HPV infection among all vaccinated women with oral and cervical HPV results. Corresponding VE against prevalent cervical HPV16/18 infection was calculated for comparison. Oral prevalence of identifiable mucosal HPV was relatively low (1·7%). Approximately four years after vaccination, there were 15 prevalent HPV16/18 infections in the control group and one in the vaccine group, for an estimated VE of 93·3% (95% CI = 63% to 100%). Corresponding efficacy against prevalent cervical HPV16/18 infection for the same cohort at the same visit was 72·0% (95% CI = 63% to 79%) (p versus oral VE = 0·04). There was no statistically significant protection against other oral HPV infections, though power was limited for these analyses.
HPV prevalence four years after vaccination with the ASO4-adjuvanted HPV16/18 vaccine was much lower among women in the vaccine arm compared to the control arm, suggesting that the vaccine affords strong protection against oral HPV16/18 infection, with potentially important implications for prevention of increasingly common HPV-associated oropharyngeal cancer. ClinicalTrials.gov, Registry number NCT00128661.
人乳头瘤病毒(HPV)感染,尤其是 16 型,导致越来越多的口咽癌病例,其发病率在增加,主要发生在发达国家。在一项针对双价 HPV 16/18 疫苗预防宫颈感染和病变的疫苗效力(VE)进行的双盲对照试验中,我们估计了接种疫苗 4 年后针对流行的口腔 HPV 感染的 VE。
共有 7466 名 18-25 岁的女性被随机分为(1∶1)接受 HPV16/18 疫苗或甲型肝炎疫苗作为对照。在最终的盲法 4 年研究访视时,5840 名参与者提供了口腔标本(合格女性的 91.9%)以评估针对口腔感染的 VE。我们的主要分析评估了所有接种疫苗的女性中口腔和宫颈 HPV 结果的流行口腔 HPV 感染。针对可比的流行宫颈 HPV16/18 感染的相应 VE 进行了计算。可识别的黏膜 HPV 的口腔流行率相对较低(1.7%)。接种疫苗大约四年后,对照组中有 15 例流行的 HPV16/18 感染,疫苗组中有 1 例,估计 VE 为 93.3%(95%CI = 63%至 100%)。同一队列在同一访视时针对流行的宫颈 HPV16/18 感染的相应疗效为 72.0%(95%CI = 63%至 79%)(与口腔 VE 相比 p = 0.04)。虽然这些分析的效力有限,但针对其他口腔 HPV 感染没有统计学意义的保护。
与对照组相比,接种 ASO4 佐剂 HPV16/18 疫苗 4 年后,疫苗组女性中 HPV 的流行率要低得多,这表明疫苗对口腔 HPV16/18 感染提供了强有力的保护,这对预防日益常见的 HPV 相关口咽癌具有重要意义。ClinicalTrials.gov,注册号 NCT00128661。