Enrolment of 22,000 adolescent women to cancer registry follow-up for long-term human papillomavirus vaccine efficacy: guarding against guessing

被引:60
|
作者
Lehtinen, Matti
Apter, Dan
Dubin, Gary
Kosunen, Elise
Isaksson, Rita
Korpivaara, Eeva-Leena
Kyha-Osterlund, Laura
Lunnas, Terhi
Luostarinen, Tapio
Niemi, Lubov
Palmroth, Johanna
Petaja, Tiina
Rekonen, Sirpa
Salmivesi, Susanna
Siitari-Mattila, Mari
Svartsjo, Sofia
Tuomivaara, Leena
Vilkki, Marjo
Pukkala, Eero
Paavonen, Jorma
机构
[1] Univ Helsinki, Dept Obstet & Gynecol, FIN-00290 Helsinki, Finland
[2] Univ Tampere, FIN-33101 Tampere, Finland
[3] Natl Publ Hlth Inst, Oulu, Finland
[4] Family Federat Finland, Helsinki, Finland
[5] Family Federat Finland, Oulu, Finland
[6] GSK Biol, King Of Prussia, PA USA
[7] Municipal Hlth Ctr Mikkeli, Mikkeli, Finland
[8] Municipal Hlth Ctr Turku, Turku, Finland
[9] Finnish Canc Registry, FIN-00170 Helsinki, Finland
[10] Municipal Hlth Ctr Kotka, Kotka, Finland
[11] Univ Kuopio, FIN-70211 Kuopio, Finland
[12] Municipal Hlth Ctr Lahti, Lahti, Finland
关键词
cervical cancer; herd immunity; prevention; vaccination;
D O I
10.1258/095646206778145550
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
carcinoma, the second most common cancer among women. Vaccination of adolescents against HPV16/18 might prevent large proportion of cervical and other anogenital cancers. However, because of ethical reasons this cannot be proven by clinical studies. To determine the long-term vaccine efficacy (VE) of HPV16/18 virus-like-particle (VLP) vaccine against cervical carcinoma in situ (CIS +) and invasive cervical carcinoma, the following three population-based cohorts of adolescent women have been enrolled: (1) women vaccinated with the HPV vaccine; (2) women vaccinated with hepatitis A control vaccine; and (3) unvaccinated control women. These cohorts will be passively followed for cumulative incidence of CIS + endpoints by population-based cancer registry. Overall 24,046 16- to 17-year-old adolescent women from 18 cities in Finland were invited between May 2004 and June 2005 to participate in a phase III trial with bivalent HPV16/18 VLP vaccine. A total of 58,996 18- to 19-year-old women were invited in May 2005 to participate as unvaccinated controls. Women who reported their willingness to participate in an HPV vaccination trial had they been 1-2 years younger were eligible. Cumulative incidence (CI) of CIS + in our cohorts over 15 years is approximately 0.45%. VE of 70% against CIS+ with 80% power requires 3357-3189 HPV16/18 vaccine recipients, 3357-3189 other vaccine recipients, and 6714-9567 unvaccinated controls. We have now enrolled 2404 HPV16/18 vaccine recipients, 2404 hepatitis A-vaccine recipients, and 5130 unvaccinated controls. This enrolment in addition to our earlier enrolment in another phase III trial guarantees enough power so that by 2020 we can ultimately provide data on the efficacy of HPV16/18 vaccination against CIS+.
引用
收藏
页码:517 / 521
页数:5
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