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HPV16 variant lineage, clinical stage, and survival in women with invasive cervical cancer
BACKGROUND: HPV16 variants are associated with different risks for development of CIN3 and invasive cancer, although all are carcinogenic. The relationship of HPV 16 variants to cancer survival has not been studied. METHODS: 155 HPV16-positive cervical cancers were categorized according to European...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3226431/ https://www.ncbi.nlm.nih.gov/pubmed/22035468 http://dx.doi.org/10.1186/1750-9378-6-19 |
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author | Zuna, Rosemary E Tuller, Erin Wentzensen, Nicolas Mathews, Cara Allen, Richard A Shanesmith, Rebecca Dunn, S Terence Gold, Michael A Wang, Sophia S Walker, Joan Schiffman, Mark |
author_facet | Zuna, Rosemary E Tuller, Erin Wentzensen, Nicolas Mathews, Cara Allen, Richard A Shanesmith, Rebecca Dunn, S Terence Gold, Michael A Wang, Sophia S Walker, Joan Schiffman, Mark |
author_sort | Zuna, Rosemary E |
collection | PubMed |
description | BACKGROUND: HPV16 variants are associated with different risks for development of CIN3 and invasive cancer, although all are carcinogenic. The relationship of HPV 16 variants to cancer survival has not been studied. METHODS: 155 HPV16-positive cervical cancers were categorized according to European and non-European variant patterns by DNA sequencing of the E6 open reading frame. Clinico-pathologic parameters and clinical outcome were collected by chart review and death registry data. RESULTS: Of the 155 women (mean age 44.7 years; median follow-up 26.7 months), 85.2% harbored European variants while 14.8% had non-European sequences. HPV16 variants differed by histologic cell type (p = 0.03) and stage (1 vs. 2+; p = 0.03). Overall, 107 women (68.0%) were alive with no evidence of cancer, 42 (27.1%) died from cervical cancer, 2 (1.3%) were alive with cervical cancer, and 4 (2.6%) died of other causes. Death due to cervical cancer was associated with European variant status (p < 0.01). While 31% of women harboring tumors with European variants died from cervical cancer during follow-up, only 1 of 23 (4.4%) non-European cases died of cancer. The better survival for non-European cases was partly mediated by lower stage at diagnosis. CONCLUSIONS: Overall, invasive cervical cancers with non-European variants showed a less aggressive behavior than those with European variants. These findings should be replicated in a population with more non-European cases. |
format | Online Article Text |
id | pubmed-3226431 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-32264312011-11-30 HPV16 variant lineage, clinical stage, and survival in women with invasive cervical cancer Zuna, Rosemary E Tuller, Erin Wentzensen, Nicolas Mathews, Cara Allen, Richard A Shanesmith, Rebecca Dunn, S Terence Gold, Michael A Wang, Sophia S Walker, Joan Schiffman, Mark Infect Agent Cancer Research Article BACKGROUND: HPV16 variants are associated with different risks for development of CIN3 and invasive cancer, although all are carcinogenic. The relationship of HPV 16 variants to cancer survival has not been studied. METHODS: 155 HPV16-positive cervical cancers were categorized according to European and non-European variant patterns by DNA sequencing of the E6 open reading frame. Clinico-pathologic parameters and clinical outcome were collected by chart review and death registry data. RESULTS: Of the 155 women (mean age 44.7 years; median follow-up 26.7 months), 85.2% harbored European variants while 14.8% had non-European sequences. HPV16 variants differed by histologic cell type (p = 0.03) and stage (1 vs. 2+; p = 0.03). Overall, 107 women (68.0%) were alive with no evidence of cancer, 42 (27.1%) died from cervical cancer, 2 (1.3%) were alive with cervical cancer, and 4 (2.6%) died of other causes. Death due to cervical cancer was associated with European variant status (p < 0.01). While 31% of women harboring tumors with European variants died from cervical cancer during follow-up, only 1 of 23 (4.4%) non-European cases died of cancer. The better survival for non-European cases was partly mediated by lower stage at diagnosis. CONCLUSIONS: Overall, invasive cervical cancers with non-European variants showed a less aggressive behavior than those with European variants. These findings should be replicated in a population with more non-European cases. BioMed Central 2011-10-28 /pmc/articles/PMC3226431/ /pubmed/22035468 http://dx.doi.org/10.1186/1750-9378-6-19 Text en Copyright ©2011 Zuna et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Zuna, Rosemary E Tuller, Erin Wentzensen, Nicolas Mathews, Cara Allen, Richard A Shanesmith, Rebecca Dunn, S Terence Gold, Michael A Wang, Sophia S Walker, Joan Schiffman, Mark HPV16 variant lineage, clinical stage, and survival in women with invasive cervical cancer |
title | HPV16 variant lineage, clinical stage, and survival in women with invasive cervical cancer |
title_full | HPV16 variant lineage, clinical stage, and survival in women with invasive cervical cancer |
title_fullStr | HPV16 variant lineage, clinical stage, and survival in women with invasive cervical cancer |
title_full_unstemmed | HPV16 variant lineage, clinical stage, and survival in women with invasive cervical cancer |
title_short | HPV16 variant lineage, clinical stage, and survival in women with invasive cervical cancer |
title_sort | hpv16 variant lineage, clinical stage, and survival in women with invasive cervical cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3226431/ https://www.ncbi.nlm.nih.gov/pubmed/22035468 http://dx.doi.org/10.1186/1750-9378-6-19 |
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