Adenocarcinoma in situ and associated human papillomavirus type distribution observed in two clinical trials of a quadrivalent human papillomavirus vaccine

The primary objective of this report is to describe the detection of adenocarcinoma in situ (AIS) and associated human papillomavirus (HPV) type distribution that was observed in the context of two phase 3 clinical trials of a quadrivalent HPV6/11/16/18 vaccine. In this intention-to-treat analysis,...

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Autores:
Tipo de recurso:
Fecha de publicación:
2011
Institución:
Universidad del Rosario
Repositorio:
Repositorio EdocUR - U. Rosario
Idioma:
eng
OAI Identifier:
oai:repository.urosario.edu.co:10336/24337
Acceso en línea:
https://doi.org/10.1002/ijc.25723
https://repository.urosario.edu.co/handle/10336/24337
Palabra clave:
Placebo
Wart virus vaccine
Adenocarcinoma in situ
Adolescent
Adult
Article
Carcinoma in situ
Colposcopy
Cytology
Disease association
Double blind procedure
Drug efficacy
Drug safety
Ethnicity
Female
Human
Human papillomavirus type 11
Human papillomavirus type 16
Human papillomavirus type 18
Human papillomavirus type 6
Human tissue
Major clinical study
Multicenter study
Nonhuman
Papillomavirus infection
Phase 3 clinical trial
Polymerase chain reaction
Priority journal
Randomized controlled trial
Uterine cervix biopsy
Uterine cervix carcinoma in situ
Adenocarcinoma
Adolescent
Adult
Cervical intraepithelial neoplasia
Colposcopy
Double-blind method
Female
Follow-up studies
Humans
Papillomaviridae
Papillomavirus infections
Papillomavirus vaccines
Prognosis
Uterine cervical neoplasms
Vaginal smears
Young adult
Adenocarcinoma in situ (ais)
Human papillomavirus (hpv)
Natural history
Vaccine
viral
Dna
Rights
License
Abierto (Texto Completo)
Description
Summary:The primary objective of this report is to describe the detection of adenocarcinoma in situ (AIS) and associated human papillomavirus (HPV) type distribution that was observed in the context of two phase 3 clinical trials of a quadrivalent HPV6/11/16/18 vaccine. In this intention-to-treat analysis, we include all women who had at least one follow-up visit postenrollment. Healthy women (17,622) aged 15-26 with no history of HPV disease and a lifetime number of less than five sex partners (average follow-up of 3.6 years) were randomized (1:1) to receive vaccine or placebo at day 1, months 2, and 6. Women underwent colposcopy and biopsy according to a Papanicolaou triage algorithm. All tissue specimens were tested for 14 HPV types and were adjudicated by a pathology panel. During the trials, 22 women were diagnosed with AIS (six vaccine and 16 placebo). There were 25 AIS lesions in total, with HPV16/18 present in 96% (24 of 25 with 15 of 25 as single infections). Only two of 22 women had concomitant cytology results suggesting glandular abnormality. Colposcopic impressions (25 total) were either negative or indicated squamous lesions only. Of women with AIS, all six in the vaccine cohort and seven of 16 in the placebo cohort were infected at baseline with the same HPV type that was detected in the AIS lesion. Concurrent squamous lesions were detected in 20 of these 22 women. In summary, our findings show that AIS evades colposcopic and cervical cytologic detection. As most AIS lesions were HPV16/18-related, prophylactic HPV vaccination should reduce the incidence of invasive adenocarcinoma. Copyright © 2011 UICC.