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      Worldwide burden of cancer attributable to HPV by site, country and HPV type

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          Abstract

          HPV is the cause of almost all cervical cancer and is responsible for a substantial fraction of other anogenital cancers and oropharyngeal cancers. Understanding the HPV‐attributable cancer burden can boost programs of HPV vaccination and HPV‐based cervical screening. Attributable fractions (AFs) and the relative contributions of different HPV types were derived from published studies reporting on the prevalence of transforming HPV infection in cancer tissue. Maps of age‐standardized incidence rates of HPV‐attributable cancers by country from GLOBOCAN 2012 data are shown separately for the cervix, other anogenital tract and head and neck cancers. The relative contribution of HPV16/18 and HPV6/11/16/18/31/33/45/52/58 was also estimated. 4.5% of all cancers worldwide (630,000 new cancer cases per year) are attributable to HPV: 8.6% in women and 0.8% in men. AF in women ranges from <3% in Australia/New Zealand and the USA to >20% in India and sub‐Saharan Africa. Cervix accounts for 83% of HPV‐attributable cancer, two‐thirds of which occur in less developed countries. Other HPV‐attributable anogenital cancer includes 8,500 vulva; 12,000 vagina; 35,000 anus (half occurring in men) and 13,000 penis. In the head and neck, HPV‐attributable cancers represent 38,000 cases of which 21,000 are oropharyngeal cancers occurring in more developed countries. The relative contributions of HPV16/18 and HPV6/11/16/18/31/33/45/52/58 are 73% and 90%, respectively. Universal access to vaccination is the key to avoiding most cases of HPV‐attributable cancer. The preponderant burden of HPV16/18 and the possibility of cross‐protection emphasize the importance of the introduction of more affordable vaccines in less developed countries.

          Abstract

          What's new?

          Most cervical cancers result from human papillomavirus (HPV) infection and therefore are preventable through screening and vaccination. Nonetheless, efforts toward HPV‐attributable cancer prevention frequently are undermined by limited access to necessary resources. The present study estimates that worldwide as many as 4.5% of new cancer cases, including cancers of the cervix, anogenital tract and head and neck, are associated with HPV infection. Cervical cancer alone accounts for 83% of those cases, most of which affect women in less‐developed countries. The findings emphasize the importance of HPV screening and vaccination and the need for less‐costly vaccines.

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          Most cited references26

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          Human Papillomavirus and Rising Oropharyngeal Cancer Incidence in the United States

          Journal of Clinical Oncology, 29(32), 4294-4301
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            Human papillomavirus and cervical cancer.

            Cervical cancer is caused by human papillomavirus infection. Most human papillomavirus infection is harmless and clears spontaneously but persistent infection with high-risk human papillomavirus (especially type 16) can cause cancer of the cervix, vulva, vagina, anus, penis, and oropharynx. The virus exclusively infects epithelium and produces new viral particles only in fully mature epithelial cells. Human papillomavirus disrupts normal cell-cycle control, promoting uncontrolled cell division and the accumulation of genetic damage. Two effective prophylactic vaccines composed of human papillomavirus type 16 and 18, and human papillomavirus type 16, 18, 6, and 11 virus-like particles have been introduced in many developed countries as a primary prevention strategy. Human papillomavirus testing is clinically valuable for secondary prevention in triaging low-grade cytology and as a test of cure after treatment. More sensitive than cytology, primary screening by human papillomavirus testing could enable screening intervals to be extended. If these prevention strategies can be implemented in developing countries, many thousands of lives could be saved. Copyright © 2013 Elsevier Ltd. All rights reserved.
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              Integrated genomic and molecular characterization of cervical cancer

              (2017)
              Cervical cancer remains one of the leading causes of cancer-related deaths worldwide. Reported here is an extensive molecular characterization of 228 primary cervical cancers, the largest comprehensive genomic study of cervical cancer to date. We observed striking APOBEC mutagenesis patterns and identified SHKBP1, ERBB3, CASP8, HLA-A, and TGFBR2 as novel significantly mutated genes in cervical cancer. We also discovered novel amplifications in immune targets CD274/PD-L1 and PDCD1LG2/PD-L2, and the BCAR4 lncRNA that has been associated with response to lapatinib. HPV integration was observed in all HPV18-related cases and 76% of HPV16-related cases, and was associated with structural aberrations and increased target gene expression. We identified a unique set of endometrial-like cervical cancers, comprised predominantly of HPV-negative tumors with high frequencies of KRAS, ARID1A, and PTEN mutations. Integrative clustering of 178 samples identified Keratin-low Squamous, Keratin-high Squamous, and Adenocarcinoma-rich subgroups. These molecular analyses reveal new potential therapeutic targets for cervical cancers.
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                Author and article information

                Contributors
                deMartelC@iarc.fr
                Journal
                Int J Cancer
                Int. J. Cancer
                10.1002/(ISSN)1097-0215
                IJC
                International Journal of Cancer
                John Wiley and Sons Inc. (Hoboken )
                0020-7136
                1097-0215
                08 June 2017
                15 August 2017
                : 141
                : 4 ( doiID: 10.1002/ijc.v141.4 )
                : 664-670
                Affiliations
                [ 1 ] International Agency for Research on Cancer Lyon France
                Author notes
                [*] [* ] Correspondence to: Dr Catherine de Martel, International Agency for Research on Cancer, 150 cours Albert Thomas, 69372 Lyon Cedex 08, France, E‐mail: deMartelC@ 123456iarc.fr ; Tel: +33 04 72 73 86 58; Fax: +33 (0)4 72 73 83 45
                Author information
                http://orcid.org/0000-0002-3642-277X
                Article
                IJC30716
                10.1002/ijc.30716
                5520228
                28369882
                079bbbff-77bc-46a5-a773-3992a48b6e3b
                © 2017 International Agency for Research on Cancer (IARC/WHO); licensed by UICC

                This is an open access article distributed under the terms of the Creative Commons Attribution IGO License IARC's preferred IGO license is the non‐commercial: https://creativecommons.org/licenses/by-nc/3.0/igo/legalcode which permits non‐commercial unrestricted use, distribution and reproduction in any medium, provided that the original work is properly cited. In any reproduction of this article there should not be any suggestion that IARC/WHO or the article endorse any specific organization or products. The use of the IARC/WHO logo is not permitted. This notice should be preserved along with the article's URL.

                History
                : 21 November 2016
                : 24 March 2017
                Page count
                Figures: 2, Tables: 3, Pages: 7, Words: 4510
                Funding
                Funded by: Fondation de France
                Award ID: 00039621
                Funded by: Bill & Melinda Gates Foundation
                Award ID: OPP1053353
                Categories
                Cancer Epidemiology
                Cancer Epidemiology
                Custom metadata
                2.0
                ijc30716
                15 August 2017
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.1.4 mode:remove_FC converted:21.07.2017

                Oncology & Radiotherapy
                human papillomavirus,cancer,attributable fraction,prevention,vaccine
                Oncology & Radiotherapy
                human papillomavirus, cancer, attributable fraction, prevention, vaccine

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