Multiple HPV genotype infection impact on invasive cervical cancer presentation and survival.

Invasive cervical cancer (ICC) is the third most common malignant neoplasm affecting Brazilian women. Little is known about the impact of specific HPV genotypes in the prognosis of ICC. We hypothesized that HPV genotype would impact ICC clinical presentation and survival.Women diagnosed with ICC at...

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Main Authors: Maria Luiza Nogueira Dias Genta, Toni Ricardo Martins, Rossana V Mendoza Lopez, José Carlos Sadalla, João Paulo Mancusi de Carvalho, Edmund Chada Baracat, José Eduardo Levi, Jesus Paula Carvalho
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5567480?pdf=render
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author Maria Luiza Nogueira Dias Genta
Toni Ricardo Martins
Rossana V Mendoza Lopez
José Carlos Sadalla
João Paulo Mancusi de Carvalho
Edmund Chada Baracat
José Eduardo Levi
Jesus Paula Carvalho
author_facet Maria Luiza Nogueira Dias Genta
Toni Ricardo Martins
Rossana V Mendoza Lopez
José Carlos Sadalla
João Paulo Mancusi de Carvalho
Edmund Chada Baracat
José Eduardo Levi
Jesus Paula Carvalho
author_sort Maria Luiza Nogueira Dias Genta
collection DOAJ
description Invasive cervical cancer (ICC) is the third most common malignant neoplasm affecting Brazilian women. Little is known about the impact of specific HPV genotypes in the prognosis of ICC. We hypothesized that HPV genotype would impact ICC clinical presentation and survival.Women diagnosed with ICC at the Instituto do Câncer do Estado de São Paulo (ICESP) between May 2008 and June 2012 were included in the study and were followed until December 2015. HPV genotype was detected from formalin-fixed paraffin-embedded (FFPE) tumor tissue samples using Onclarity™ system (BD Viper™ LT automated system).292 patients aged 50±14 years were analyzed. HPVDNA was detected in 84% of patients. The HPV genotypes studied were: HPV16 (64%), HPV18 (10%), HPV33-58 (7%), HPV45 (5%), HPV31 (4%) and other high-risk HPV genotypes (11%). HPV genotypes showed different distributions regarding histological type and clinical stage. Patients were followed for 35±21 months. The overall survival at 5 years after diagnosis of cervical cancer was 54%. Age, clinical staging, histological type and multiple HPV genotypes infection detected in the same tumor specimen were associated with poorer overall survival on multivariate Cox proportional hazard analysis (p<0.05). No specific HPV genotype affected survival.Multiple HPV genotype infection was associated with poorer ICC survival in our study, compared with single genotype infection. HPV genotyping from FFPE tumor tissue using an automated assay such as the Onclarity BD™ assay provides a simpler alternative for routine clinical use.This is the largest study employing an automated HPV genotyping assay using FFPE of ICC. Multiple HPV genotype infection adversely influenced survival.
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spelling doaj.art-49f002d3ea6c4cac85bddec14c1b4a572022-12-22T01:32:03ZengPublic Library of Science (PLoS)PLoS ONE1932-62032017-01-01128e018285410.1371/journal.pone.0182854Multiple HPV genotype infection impact on invasive cervical cancer presentation and survival.Maria Luiza Nogueira Dias GentaToni Ricardo MartinsRossana V Mendoza LopezJosé Carlos SadallaJoão Paulo Mancusi de CarvalhoEdmund Chada BaracatJosé Eduardo LeviJesus Paula CarvalhoInvasive cervical cancer (ICC) is the third most common malignant neoplasm affecting Brazilian women. Little is known about the impact of specific HPV genotypes in the prognosis of ICC. We hypothesized that HPV genotype would impact ICC clinical presentation and survival.Women diagnosed with ICC at the Instituto do Câncer do Estado de São Paulo (ICESP) between May 2008 and June 2012 were included in the study and were followed until December 2015. HPV genotype was detected from formalin-fixed paraffin-embedded (FFPE) tumor tissue samples using Onclarity™ system (BD Viper™ LT automated system).292 patients aged 50±14 years were analyzed. HPVDNA was detected in 84% of patients. The HPV genotypes studied were: HPV16 (64%), HPV18 (10%), HPV33-58 (7%), HPV45 (5%), HPV31 (4%) and other high-risk HPV genotypes (11%). HPV genotypes showed different distributions regarding histological type and clinical stage. Patients were followed for 35±21 months. The overall survival at 5 years after diagnosis of cervical cancer was 54%. Age, clinical staging, histological type and multiple HPV genotypes infection detected in the same tumor specimen were associated with poorer overall survival on multivariate Cox proportional hazard analysis (p<0.05). No specific HPV genotype affected survival.Multiple HPV genotype infection was associated with poorer ICC survival in our study, compared with single genotype infection. HPV genotyping from FFPE tumor tissue using an automated assay such as the Onclarity BD™ assay provides a simpler alternative for routine clinical use.This is the largest study employing an automated HPV genotyping assay using FFPE of ICC. Multiple HPV genotype infection adversely influenced survival.http://europepmc.org/articles/PMC5567480?pdf=render
spellingShingle Maria Luiza Nogueira Dias Genta
Toni Ricardo Martins
Rossana V Mendoza Lopez
José Carlos Sadalla
João Paulo Mancusi de Carvalho
Edmund Chada Baracat
José Eduardo Levi
Jesus Paula Carvalho
Multiple HPV genotype infection impact on invasive cervical cancer presentation and survival.
PLoS ONE
title Multiple HPV genotype infection impact on invasive cervical cancer presentation and survival.
title_full Multiple HPV genotype infection impact on invasive cervical cancer presentation and survival.
title_fullStr Multiple HPV genotype infection impact on invasive cervical cancer presentation and survival.
title_full_unstemmed Multiple HPV genotype infection impact on invasive cervical cancer presentation and survival.
title_short Multiple HPV genotype infection impact on invasive cervical cancer presentation and survival.
title_sort multiple hpv genotype infection impact on invasive cervical cancer presentation and survival
url http://europepmc.org/articles/PMC5567480?pdf=render
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