Persistent high-risk human papillomavirus (HPV) infections as surrogate endpoints of progressive cervical disease. Potential new endpoint for efficacy studies with new-generation (non-HPV16/18) prophylactic HPV vaccines

European Journal of Gynaecological Oncology

Volumn 32, Issue 1, 2011, Pages 17-33

  Syrjanen K ^a  

^a TURKU UNIVERSITY HOSPITAL   (Finland)

Author keywords

6 mo and 12 mo persistence; Efficacy trials; High risk types; HPV vaccines; Human papillomavirus; LAMS study; NIS cohort; Persistent infection; Progressive disease; Study power; Surrogate endpoint

Indexed keywords

VIRUS DNA; WART VIRUS VACCINE;

ARTICLE; CANCER RISK; DISEASE COURSE; DISEASE DURATION; FEMALE; FOLLOW UP; HUMAN; HUMAN PAPILLOMAVIRUS TYPE 16; HUMAN PAPILLOMAVIRUS TYPE 18; HUMAN PAPILLOMAVIRUS TYPE 31; HUMAN PAPILLOMAVIRUS TYPE 33; HUMAN PAPILLOMAVIRUS TYPE 35; META ANALYSIS (TOPIC); PAPANICOLAOU TEST; PAPILLOMAVIRUS INFECTION; PERISTENT HIGH RISK HUMAN PAPILLOMAVIRUS INFECTION; PERSISTENT VIRUS INFECTION; RISK; RISK ASSESSMENT; UTERINE CERVIX CANCER; UTERINE CERVIX DISEASE;

BIOLOGICAL MARKERS; CERVICAL INTRAEPITHELIAL NEOPLASIA; COHORT STUDIES; DISEASE PROGRESSION; FEMALE; HUMANS; PAPILLOMAVIRUS INFECTIONS; PAPILLOMAVIRUS VACCINES; UTERINE CERVICAL NEOPLASMS;

EID: 79952327378     PISSN: 03922936     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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