Immunogenicity of 2 Doses of HPV Vaccine in Younger Adolescents vs 3 Doses in Young Women A Randomized Clinical Trial

被引:327
作者
Dobson, Simon R. M. [1 ,6 ]
McNeil, Shelly [7 ]
Dionne, Marc [9 ]
Dawar, Meena [2 ,10 ]
Ogilvie, Gina [2 ,11 ]
Krajden, Mel [3 ,11 ]
Sauvageau, Chantal [9 ]
Scheifele, David W. [1 ,6 ]
Kollmann, Tobias R. [1 ,6 ]
Halperin, Scott A. [8 ]
Langley, Joanne M. [8 ]
Bettinger, Julie A. [1 ,6 ]
Singer, Joel [2 ]
Money, Deborah [4 ]
Miller, Dianne [4 ,12 ]
Naus, Monika [2 ,11 ]
Marra, Fawziah [5 ,11 ]
Young, Eric [13 ]
机构
[1] Univ British Columbia, Dept Pediat, Vancouver, BC V5Z 4H4, Canada
[2] Univ British Columbia, Sch Populat & Publ Hlth, Vancouver, BC V5Z 4H4, Canada
[3] Univ British Columbia, Dept Pathol & Lab Med, Vancouver, BC V5Z 4H4, Canada
[4] Univ British Columbia, Dept Obstet & Gynaecol, Vancouver, BC V5Z 4H4, Canada
[5] Univ British Columbia, Fac Pharmaceut Sci, Vancouver, BC V5Z 4H4, Canada
[6] Vaccine Evaluat Ctr, Vancouver, BC, Canada
[7] Dalhousie Univ, IWK Hlth Ctr & Capital Hlth, Canadian Ctr Vaccinol, Dept Med, Halifax, NS B3H 3J5, Canada
[8] Dalhousie Univ, IWK Hlth Ctr & Capital Hlth, Canadian Ctr Vaccinol, Dept Pediat, Halifax, NS B3H 3J5, Canada
[9] Ctr Hosp Univ Quebec, Quebec City, PQ, Canada
[10] Vancouver Coastal Hlth Author, Vancouver, BC, Canada
[11] British Columbia Ctr Dis Control, Vancouver, BC, Canada
[12] British Columbia Canc Agcy, Vancouver, BC V5Z 4E6, Canada
[13] British Columbia Minist Hlth, Vancouver, BC, Canada
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 2013年 / 309卷 / 17期
关键词
HUMAN-PAPILLOMAVIRUS TYPE-6; PARTICLE VACCINE; NEUTRALIZING EPITOPES; ANTIBODIES; RESPONSES; EFFICACY; SAFETY; 2-DOSE; ASSAY;
D O I
10.1001/jama.2013.1625
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:1793 / 1802
页数:10
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