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Evaluation of Type Replacement Following HPV16/18 Vaccination: Pooled Analysis of Two Randomized Trials.
- Source :
-
Journal of the National Cancer Institute [J Natl Cancer Inst] 2017 Jan 28; Vol. 109 (7). Date of Electronic Publication: 2017 Jan 28 (Print Publication: 2017). - Publication Year :
- 2017
-
Abstract
- Background: Current HPV vaccines do not protect against all oncogenic HPV types. Following vaccination, type replacement may occur, especially if different HPV types competitively interact during natural infection. Because of their common route of transmission, it is difficult to assess type interactions in observational studies. Our aim was to evaluate type replacement in the setting of HPV vaccine randomized controlled trials (RCTs).<br />Methods: Data were pooled from the Costa Rica Vaccine Trial (CVT; NCT00128661) and PATRICIA trial (NCT001226810)-two large-scale, double-blind RCTs of the HPV-16/18 AS04-adjuvanted vaccine-to compare cumulative incidence of nonprotected HPV infections across trial arms after four years. Negative rate difference estimates (rate in control minus vaccine arm) were interpreted as evidence of replacement if the associated 95% confidence interval excluded zero. All statistical tests were two-sided.<br />Results: After applying relevant exclusion criteria, 21 596 women were included in our analysis (HPV arm = 10 750; control arm = 10 846). Incidence rates (per 1000 infection-years) were lower in the HPV arm than in the control arm for grouped nonprotected oncogenic types (rate difference = 1.6, 95% confidence interval [CI] = 0.9 to 2.3) and oncogenic/nononcogenic types (rate difference = 0.2, 95% CI = -0.3 to 0.7). Focusing on individual HPV types separately, no deleterious effect was observed. In contrast, a statistically significant protective effect (positive rate difference and 95% CI excluded zero) was observed against oncogenic HPV types 35, 52, 58, and 68/73, as well as nononcogenic types 6 and 70.<br />Conclusion: HPV type replacement does not occur among vaccinated individuals within four years and is unlikely to occur in vaccinated populations.<br /> (Published by Oxford University Press 2016. This work is written by US Government employees and is in the public domain in the US.)
- Subjects :
- Adolescent
Adult
Costa Rica
Double-Blind Method
Female
Follow-Up Studies
Humans
Papillomavirus Infections immunology
Papillomavirus Infections virology
Papillomavirus Vaccines immunology
Treatment Outcome
Uterine Cervical Neoplasms immunology
Uterine Cervical Neoplasms virology
Vaccination methods
Young Adult
Uterine Cervical Dysplasia immunology
Uterine Cervical Dysplasia virology
Human papillomavirus 16 immunology
Human papillomavirus 18 immunology
Papillomavirus Infections prevention & control
Papillomavirus Vaccines therapeutic use
Uterine Cervical Neoplasms prevention & control
Uterine Cervical Dysplasia prevention & control
Subjects
Details
- Language :
- English
- ISSN :
- 1460-2105
- Volume :
- 109
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- Journal of the National Cancer Institute
- Publication Type :
- Academic Journal
- Accession number :
- 28132019
- Full Text :
- https://doi.org/10.1093/jnci/djw300