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Your browser does not have JavaScript enabled and some parts of this website will not work without it. The site you are about to visit is a site maintained by a third party, which is in complete control of its content. Current practice can involve repeating both Pap cytology and pooled hrHPV DNA testing in 12 months for women with normal cytology and a positive hrHPV DNA result instead of referring them for colposcopy. Since HPV 16 and 18 confer a higher risk of having precancerous lesions and cervical cancer than other genotypes,2 focusing on these genotypes gives the physician useful details upon which to make effective treatment decisions. Today, as is supported by ACOG,3 individual genotyping is a follow-up test subsequent to a normal Pap smear and a positive pooled HPV testing result. Of the 14 oncogenic HPV genotypes, HPV 16 and 18 cause approximately two-thirds of cervical cancers worldwide.
This website contains information on products which is targeted to a wide range of audiences and could contain product details or information otherwise not accessible or valid in your country. The cobas® HPV Test - the only FDA approved and CE-IVD marked HPV test for first-line, primary screening.
The cervical cancer screening and management guidelines outlined below are recommended by professional societies in the United States, including the American Society for Colposcopy and Cervical Pathology (ASCCP), the American Society for Clinical Pathology (ASCP), and the American Cancer Society (ACS).
View all of the ASCCP Updated Consensus Guidelines for the Management of Women with Cervical Cytological Abnormalities algorithms. Download the ASCCP Updated Consensus Guidelines for Managing Abnormal Cervical Cancer Screening Tests and Cancer Precursors App from Google play or the iTunes App Store. In March 2012, new guidelines for the prevention and early detection of cervical cancer were issued jointly by the American Cancer Society (ACS), the American Society for Colposcopy and Cervical Pathology (ASCCP), and the American Society for Clinical Pathology (ASCP).
Using human papillomavirus (HPV) testing in addition to a Pap test (also known as co-testing) is preferable to using a Pap test alone for women ages 30 – 65 years. Individual genotyping for HPV 16 or HPV 16 and 18 recommended as an option for hrHPV+ women with normal cytology. Moreover, the societies now recommend that individual genotyping for HPV 16 or HPV 16 and 18 may be used when women have a negative cytology (Pap test) but have positive results on a test for “pooled” high-risk HPV types.
Roche’s landmark ATHENA study is cited by the professional organizations as a central study providing the evidence for differential patient management based on HPV 16 and 18 DNA genotyping.


Women with a history of CIN2 or a more severe diagnosis should continue routine screening for at least 20 years. Applies to women without a cervix and without a history of CIN2 or a more severe diagnosis in the past 20 years of cervical cancer ever.
Guidelines were developed based on HPV tests that have performance characteristics similar to those of the HPV tests used in the supporting evidence. Testing for low-risk HPV types has no clinical role in cervical cancer screening or the evaluation of women with abnormal cytology. In women 30 years and older the test may be used adjunctively with the Cervista HPV HR test in combination with cervical cytology to assess the presence or absence of specific high-risk HPV types 16 and 18. Can be used adjunctively with the Cervista HPV HR test in patients with ASC-US cervical cytology results, to assess the presence or absence of high-risk types 16 and 18. Laboratory will have extracted DNA from the high-risk test up to 1 month after the high-risk test is performed. El sitio que estara visitando es un sitio mantenido por un tercero, que posee el control completo de su contenido. La practica actual puede abarcar ambas pruebas conjuntamente, la citologia por Pap y la prueba de grupo o (pool) de ADN del hrHPV en 12 meses para mujeres con citologia normal y un resultado positivo de ADN del VPH de alto riesgo (hrHPV), en lugar de enviar a las mujeres a colposcopia.
Incertidumbre y ansiedad de ambas partes, medico y paciente, cuando la paciente tiene citologia normal y resultado de ADN del hrHPV es positivo. Ya que el VPH 16 y 18 confieren un mayor riesgo de tener lesiones precancerosas y cancer cervical que otros genotipos,2 enfocarse a estos genotipos proporciona al medico detalles utiles sobre como tomar las decisiones mas efectivas de tratamiento.
Actualmente, como es apoyado por ACOG,3 la genotipificacion individual es una prueba de seguimiento subsecuente a un pap normal y de un resultado positivo de grupo pool de las pruebas de VPH. De los 14 tipos de VPH oncogenico, el VPH 16 y 18 causan aproximadamente dos tercios de los casos de cancer cervical en todo el mundo.
Las mujeres que tuvieron infeccion persistente por VPH16 tuvieron un 50%   aproximadamente de riesgo ?CIN3 en 12 anos. Esta pagina web contiene informacion de productos que estan dirigidos a una amplia audiencia y podria contener detalles del producto o informacion que no es accesible o valida en su pais. In the skin papilloma virus can cause different types of warts and in the ano-genital region it is associated with condyloma or carcinoma.


Roche Diagnostics does not control, influence, or endorse this site and the opinions, claims, or comments expressed on this site  should not be attributed to Roche Diagnostics. Please be aware that we do not take any responsibility for accessing such information which may not comply with any valid legal process, regulation, registration or usage in the country of your origin.
Roche Molecular Systems does not control, influence, or endorse this site and the opinions, claims, or comments expressed on this site should not be attributed to Roche Molecular Systems.
Human papillomavirus-18 merits special consideration because of its association with cervical adenocarcinomas, which are less efficiently detected by cytology than squamous cancers. Roche Molecular Systems no tiene el control, influencia o avala este sitio y las opiniones, reclamaciones o comentarios expresados en este sitio , los cuales no deben ser atribuidos a Roche Molecular Systems. Por favor tenga en cuenta que no asumimos ninguna responsabilidad por el acceso a tal informacion que pudiera no estar de acuerdo con algun proceso legal, reglamentacion, registro o uso en el pais de su origen. HPV types 1,6 and 11 usually are associated with benign transformations of the tissues, while e.g. The elevated 10-year risk of cervical precancer and cancer in women with human papillomavirus (HPV) type 16 or 18 and the possible utility of type-specific HPV testing in clinical practice. Preferential risk of HPV16 for squamous cell carcinoma and of HPV18 for adenocarcinoma of the cervix compared to women with normal cytology in The Netherlands.
Adenocarcinoma in situ and associated human papillomavirus type distribution observed in two clinical trials of a quadrivalent human papillomavirus vaccine. Human papillomavirus genotype attribution in invasive cervical cancer: a retrospective cross-sectional worldwide study.
Long-term absolute risk of cervical intraepithelial neoplasia grade 3 or worse following human papillomavirus infection: role of persistence.
Clinical Management Guidelines for Obstetrician-Gynecologists: Screening for Cervical Cancer.
HPV types 16, 18 and 31 seem to be responsible for the development of some carcinoma like cervical carcinoma.



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