Department of Pediatrics, University of British Columbia, Vancouver, Canada.
JAMA. 2013 May 1;309(17):1793-802. doi: 10.1001/jama.2013.1625.
Global use of human papillomavirus (HPV) vaccines to prevent cervical cancer is impeded by cost. A 2-dose schedule for girls may be possible.
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%).
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.
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.
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.
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.
clinicaltrials.gov Identifier: NCT00501137.
全球使用人乳头瘤病毒(HPV)疫苗预防宫颈癌受到成本的阻碍。为女孩接种两剂方案可能是可行的。
确定接受两剂方案的女孩的 HPV-16 和 HPV-18 抗体水平是否与接受三剂方案的女性相当。
设计、地点和患者:2007 年 8 月至 2011 年 2 月,在加拿大进行的一项随机、3 期、上市后、多中心、按年龄分层、非劣效性免疫原性研究,共纳入 830 名女性,随访血样由 675 名参与者(81%)提供。
女孩(9-13 岁)按 1:1 随机分为两组,一组接受四价 HPV 疫苗 0、2 和 6 个月接种(n=261),另一组接受两剂 0 和 6 个月接种(n=259)。年轻女性(16-26 岁)接受 0、2 和 6 个月接种(n=310)。在 0、7、18、24 和 36 个月测量抗体水平。
主要终点为 1 个月时最后一剂后女孩(两剂)与年轻女性(三剂)的 HPV-16 和 HPV-18 几何平均滴度(GMT)比值的非劣效性(95%置信区间,下限>0.5)。次要终点为接受两剂与三剂疫苗的女孩的 GMT 比值的非劣效性;以及 36 个月时非劣效性的持久性。
女孩(两剂)与女性(三剂)的 GMT 比值具有非劣效性:HPV-16 为 2.07(95%置信区间,1.62-2.65),HPV-18 为 1.76(95%置信区间,1.41-2.19)。女孩(三剂)在最后一次接种后 1 个月,HPV-16 的 GMT 反应为 7736 毫梅克单位/毫升(mMU/mL)(95%置信区间,6651-8999),HPV-18 的 GMT 反应为 1730 mMU/mL(95%置信区间,1512-1980)。女孩(两剂)与女孩(三剂)的 GMT 比值具有非劣效性:HPV-16 为 0.95(95%置信区间,0.73-1.23),HPV-18 为 0.68(95%置信区间,0.54-0.85)。在 36 个月时,女孩(两剂)与女性(三剂)的 GMT 比值对所有基因型均具有非劣效性。在 7 个月时,女孩接种两剂与接种三剂后对所有 4 种疫苗基因型的抗体反应均具有非劣效性,但在 24 个月时对 HPV-18 或 36 个月时对 HPV-6 不具有非劣效性。
在接受两剂 HPV 疫苗接种的女孩中,最后一剂后一个月对 HPV-16 和 HPV-18 的反应与接受三剂疫苗接种的年轻女性相当。由于在接种两剂和三剂的女孩中,24 至 36 个月时某些基因型的非劣效性丧失,因此在推荐减少剂量方案之前,需要更多关于保护持续时间的数据。
clinicaltrials.gov 标识符:NCT00501137。