Infections with oncogenic types of HPV cause virtually all cases of cervical cancer worldwide. Prophylactic vaccination against HPV 16 and 18, two of the most important HPV types, could protect against a large majority of the cases of cervical cancer globally. Vaccines based on the L1 structural protein of HPV that self-assemble intoconformationally-correct virion-like particles (virus-like particles or VLPs) are under study.The immunogenicity and safety of HPV 16 & 18 VLPs have been demonstrated in Phase 1 and Phase 2 human trials. Evidence also suggest high efficacy of VLP-based vaccines in protecting against type-specific persistent HPV infection and associated lesions. Two VLP-based vaccines are being developed; one has recently been approved for use. The second is expected to be approved for use in the near future.A full-scale Phase 3 randomized controlled trial of an HPV16/18 VLP vaccine has been initiated in Costa Rica. Costa Rica was chosen for the Phase 3 trial because of our extensive successful scientific collaborations there,the continued high risk of cervical cancer, the universal medical system providing national linkage, and the likelihood of very high participation over the many needed years of close clinical follow-up. Randomization and 3-dose vaccination of 7,466 women enrolled into the HPV-16/18 Vaccine Trial in Costa Rica has been successfully completed. Four years of active follow-up are planned for each participant. Should the vaccine be proven to be safe and effective, and to provide protection against HPV infection for several years, cross-over vaccination will be offered to trial participants. This cross-over will occur at the end of follow-up or sooner, if recommended by the trial Data and Safety Monitoring Board (DSMB) and approved by the Institutional Review Boards (IRBs) overseeing the trial. Four years of follow-up will be provided to participants regardless of the timing of cross-over vaccination.In support of the vaccine trials, a variety of methodologic and ancillary projects are underway or planned, that willmaximize the yield of the main effort.

Agency
National Institute of Health (NIH)
Institute
Division of Cancer Epidemiology And Genetics (NCI)
Type
Intramural Research (Z01)
Project #
1Z01CP010177-06
Application #
7330839
Study Section
(HREB)
Project Start
Project End
Budget Start
Budget End
Support Year
6
Fiscal Year
2006
Total Cost
Indirect Cost
Name
Cancer Epidemiology and Genetics
Department
Type
DUNS #
City
State
Country
United States
Zip Code
Lowy, Douglas R; Herrero, Rolando; Hildesheim, Allan et al. (2015) Primary endpoints for future prophylactic human papillomavirus vaccine trials: towards infection and immunobridging. Lancet Oncol 16:e226-33
Hildesheim, Allan; Wacholder, Sholom; Catteau, Gregory et al. (2014) Efficacy of the HPV-16/18 vaccine: final according to protocol results from the blinded phase of the randomized Costa Rica HPV-16/18 vaccine trial. Vaccine 32:5087-97
Herrero, Rolando; Wacholder, Sholom; Rodríguez, Ana C et al. (2011) Prevention of persistent human papillomavirus infection by an HPV16/18 vaccine: a community-based randomized clinical trial in Guanacaste, Costa Rica. Cancer Discov 1:408-19
Baker, Rosalyn; Dauner, Joseph G; Rodriguez, Ana Cecilia et al. (2011) Increased plasma levels of adipokines and inflammatory markers in older women with persistent HPV infection. Cytokine 53:282-5
Herrero, Rolando; Hildesheim, Allan; Rodriguez, Ana C et al. (2008) Rationale and design of a community-based double-blind randomized clinical trial of an HPV 16 and 18 vaccine in Guanacaste, Costa Rica. Vaccine 26:4795-808
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