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Population-Based Assessment of HPV Genotype-Specific Cervical Cancer Survival: CDC Cancer Registry Sentinel Surveillance System.
Hallowell, Benjamin D; Saraiya, Mona; Thompson, Trevor D; Unger, Elizabeth R; Lynch, Charles F; Tucker, Tom; Copeland, Glenn; Hernandez, Brenda Y; Peters, Edward S; Wilkinson, Edward; Goodman, Marc T.
Afiliação
  • Hallowell BD; Centers for Disease Control and Prevention, Atlanta, GA.
  • Saraiya M; Centers for Disease Control and Prevention, Atlanta, GA.
  • Thompson TD; Centers for Disease Control and Prevention, Atlanta, GA.
  • Unger ER; Centers for Disease Control and Prevention, Atlanta, GA.
  • Lynch CF; University of Iowa, Iowa City, IA.
  • Tucker T; University of Kentucky College of Public Health, Lexington, KY.
  • Copeland G; Michigan Department of Community Health, Lansing, MI.
  • Hernandez BY; University of Hawaii, Honolulu, HI.
  • Peters ES; Health Science Center School of Public Health, Lousiania State University, New Orleans, LA.
  • Wilkinson E; Department of Pathology, University of Florida College of Medicine, Gainesville, FL.
  • Goodman MT; Cedars Sinai Medical Center, Los Angeles, CA.
JNCI Cancer Spectr ; 2(3)2018 07.
Article em En | MEDLINE | ID: mdl-30596199
ABSTRACT

Background:

Human papillomavirus (HPV) genotype influences the development of invasive cervical cancer (ICC); however, there is uncertainty regarding the association of HPV genotype with survival among ICC patients.

Methods:

Follow-up data were collected from 693 previously selected and HPV-typed ICC cases that were part of the Centers for Disease Control and Prevention Cancer Registry Surveillance System. Cases were diagnosed between 1994 and 2005. The Kaplan-Meier method was used to estimate five-year all-cause survival. A multivariable Cox proportional hazards model was used to estimate the effect of HPV genotype on survival after adjusting for demographic, tumor, and treatment characteristics.

Results:

Five-year all-cause survival rates varied by HPV status (HPV 16 66.9%, HPV 18 65.7%, HPV 31/33/45/52/58 70.8%, other oncogenic HPV genotypes 79.0%, nononcogenic HPV 69.3%, HPV-negative 54.0%). Following multivariable adjustment, no statistically significant survival differences were found for ICC patients with HPV 16-positive tumors compared with women with tumors positive for HPV 18, other oncogenic HPV types, or HPV-negative tumors. Women with detectable HPV 31/33/33/45/52/58 had a statistically significant 40% reduced hazard of death at five years (95% confidence interval [CI] = 0.38 to 0.95), and women who tested positive for nononcogenic HPV genotypes had a statistically significant 57% reduced hazard of death at five years (95% CI = 0.19 to 0.96) compared with women with HPV 16 tumors. Few statistically significant differences in HPV positivity, tumor characteristics, treatment, or survival were found by race/ethnicity.

Conclusions:

HPV genotype statistically significantly influenced five-year survival rates among women with ICC; however, screening and HPV vaccination remain the most important factors to improve patient prognosis and prevent future cases.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Screening_studies Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Screening_studies Idioma: En Ano de publicação: 2018 Tipo de documento: Article