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Immunogenicity of 2 doses of HPV vaccine in younger adolescents vs 3 doses in young women: A randomized clinical trial

机译:青春期2剂HPV疫苗与年轻女性3剂的免疫原性:一项随机临床试验

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Importance: Global use of human papillomavirus (HPV) vaccines to prevent cervical cancer is impeded by cost. A 2-dose schedule for girls may be possible. Objective: To determine whether mean antibody levels to HPV-16 and HPV-18 among girls receiving 2 doses was noninferior to women receiving 3 doses. Design, Setting, and Patients: Randomized, phase 3, postlicensure, multicenter, age-stratified, noninferiority immunogenicity study of 830 Canadian females from August 2007 through February 2011. Follow-up blood samples were provided by 675 participants (81%). Intervention: Girls (9-13 years) were randomized 1:1 to receive 3 doses of quadrivalent HPV vaccine at 0, 2, and 6 months (n = 261) or 2 doses at 0 and 6 months (n = 259). Young women (16-26 years) received 3 doses at 0, 2, and 6 months (n = 310). Antibody levels were measured at 0, 7, 18, 24, and 36 months. Main Outcomes and Measures: Primary outcome was noninferiority (95% CI, lower bound >0.5) of geometric mean titer (GMT) ratios for HPV-16 and HPV-18 for girls (2 doses) compared with young women (3 doses) 1 month after last dose. Secondary outcomes were noninferiority of GMT ratios of girls receiving 2 vs 3 doses of vaccine; and durability of noninferiority to 36 months. Results: The GMT ratios were noninferior for girls (2 doses) to women (3 doses): 2.07 (95% CI, 1.62-2.65) for HPV-16 and 1.76 (95% CI, 1.41-2.19) for HPV-18. Girls (3 doses) had GMT responses 1 month after last vaccination for HPV-16 of 7736 milli-Merck units per mL (mMU/mL) (95% CI, 6651-8999) and HPV-18 of 1730 mMU/mL (95% CI, 1512-1980). The GMT ratios were noninferior for girls (2 doses) to girls (3 doses): 0.95 (95% CI, 0.73-1.23) for HPV-16 and 0.68 (95% CI, 0.54-0.85) for HPV-18. The GMT ratios for girls (2 doses) to women (3 doses) remained noninferior for all genotypes to 36 months. Antibody responses in girls were noninferior after 2 doses vs 3 doses for all 4 vaccine genotypes at month 7, but not for HPV-18 by month 24 or HPV-6 by month 36. Conclusions and Relevance: Among girls who received 2 doses of HPV vaccine 6 months apart, responses to HPV-16 and HPV-18 one month after the last dose were noninferior to those among young women who received 3 doses of the vaccine within 6 months. Because of the loss of noninferiority to some genotypes at 24 to 36 months in girls given 2 doses vs 3 doses, more data on the duration of protection are needed before reduced-dose schedules can be recommended. Trial Registration: clinicaltrials.gov Identifier: NCT00501137.
机译:重要性:成本阻碍了全球使用人乳头瘤病毒(HPV)疫苗预防子宫颈癌。可能有2剂供女孩服用的时间表。目的:确定接受2剂治疗的女孩中HPV-16和HPV-18的平均抗体水平是否不低于接受3剂治疗的女性。设计,地点和患者:2007年8月至2011年2月,对830名加拿大女性进行的随机,3期,许可后,多中心,年龄分层,非劣效性免疫原性研究。随访的血液样本由675名参与者提供(81%)。干预:女孩(9-13岁)以1:1的比例随机分配,分别在0、2和6个月(n = 261)接受3剂四价HPV疫苗或在0和6个月(n = 259)接受2剂。年轻妇女(16-26岁)分别在0、2和6个月接受3剂(n = 310)。在0、7、18、24和36个月时测量抗体水平。主要结果和措施:主要结果是女孩(2剂)与女性(3剂)相比,女孩(2剂)的HPV-16和HPV-18的几何平均滴度(GMT)比率为劣等(95%CI,下界> 0.5)1最后一剂后一个月。次要结果是接受2剂和3剂疫苗的女孩的GMT比率非劣;和非劣质性的持久性至36个月。结果:女孩(2剂)对女性(3剂)的GMT比率不亚于:HPV-16为2.07(95%CI,1.62-2.65),HPV-18为1.76(95%CI,1.41-2.19)。上次接种疫苗后1个月,女孩(3剂)对HPV-16的GMT反应为7736毫默克/ mL(mMU / mL)(95%CI,6651-8999),HPV-18为1730 mMU / mL(95 CI(1512-1980)。 GMT比率在女孩(2剂)与女孩(3剂)之间不亚于:HPV-16为0.95(95%CI,0.73-1.23),HPV-18为0.68(95%CI,0.54-0.85)。在所有基因型至36个月内,女孩(2剂)对妇女(3剂)的GMT比率均不逊色。 2剂后女孩的抗体反应不劣于7个月时所有4种疫苗基因型的3剂,但在24个月时对HPV-18或36个月时对HPV-6并非如此。结论和相关性:在接受2剂HPV的女孩中疫苗相距6个月,在最后一次注射后1个月对HPV-16和HPV-18的反应不逊于在6个月内接受3剂疫苗的年轻女性。由于在给予2剂vs 3剂的女孩中,某些基因型在24至36个月时不会丧失自卑性,因此在建议减少剂量方案之前,需要更多有关保护期的数据。试用注册:clinicaltrials.gov标识符:NCT00501137。

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