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DOI 10.1093/jnci/djv302

Медицинская библиотека · Journal of the National Cancer Institute · 2015

Multisite HPV16/18 Vaccine Efficacy Against Cervical, Anal, and Oral HPV Infection.

Beachler Daniel C, Kreimer Aimée R, Schiffman Mark, Herrero Rolando, Wacholder Sholom, Rodriguez Ana Cecilia, Lowy Douglas R, Porras Carolina, Schiller John T, Quint Wim, Jimenez Silvia, Safaeian Mahboobeh, Struijk Linda, Schussler John, Hildesheim Allan, Gonzalez Paula, Costa Rica HPV Vaccine Trial (CVT) Group

СтатьяРандомизированное исследованиеПоддержка NIH: внешняя программаПоддержка правительства СШАПеревод пока не подготовлен

Аннотация

BACKGROUND

Previous Costa Rica Vaccine Trial (CVT) reports separately demonstrated vaccine efficacy against HPV16 and HPV18 (HPV16/18) infections at the cervical, anal, and oral regions; however, the combined overall multisite efficacy (protection at all three sites) and vaccine efficacy among women infected with HPV16 or HPV18 prior to vaccination are less known.

METHODS

Women age 18 to 25 years from the CVT were randomly assigned to the HPV16/18 vaccine (Cervarix) or a hepatitis A vaccine. Cervical, oral, and anal specimens were collected at the four-year follow-up visit from 4186 women. Multisite and single-site vaccine efficacies (VEs) and 95% confidence intervals (CIs) were computed for one-time detection of point prevalent HPV16/18 in the cervical, anal, and oral regions four years after vaccination. All statistical tests were two-sided.

RESULTS

The multisite woman-level vaccine efficacy was highest among "naïve" women (HPV16/18 seronegative and cervical HPV high-risk DNA negative at vaccination) (vaccine efficacy = 83.5%, 95% CI = 72.1% to 90.8%). Multisite woman-level vaccine efficacy was also demonstrated among women with evidence of a pre-enrollment HPV16 or HPV18 infection (seropositive for HPV16 and/or HPV18 but cervical HPV16/18 DNA negative at vaccination) (vaccine efficacy = 57.8%, 95% CI = 34.4% to 73.4%), but not in those with cervical HPV16 and/or HPV18 DNA at vaccination (anal/oral HPV16/18 VE = 25.3%, 95% CI = -40.4% to 61.1%). Concordant HPV16/18 infections at two or three sites were also less common in HPV16/18-infected women in the HPV vaccine vs control arm (7.4% vs 30.4%, P < .001).

CONCLUSIONS

This study found high multisite vaccine efficacy among "naïve" women and also suggests the vaccine may provide protection against HPV16/18 infections at one or more anatomic sites among some women infected with these types prior to HPV16/18 vaccination.

Для цитирования: Beachler Daniel C, Kreimer Aimée R, Schiffman Mark, Herrero Rolando, Wacholder Sholom, Rodriguez Ana Cecilia, Lowy Douglas R, Porras Carolina, Schiller John T, Quint Wim, Jimenez Silvia, Safaeian Mahboobeh, Struijk Linda, Schussler John, Hildesheim Allan, Gonzalez Paula, Costa Rica HPV Vaccine Trial (CVT) Group. Multisite HPV16/18 Vaccine Efficacy Against Cervical, Anal, and Oral HPV Infection.. Journal of the National Cancer Institute. 2015. DOI: 10.1093/jnci/djv302.

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