Artigo Acesso aberto Revisado por pares

Uptake of co-testing with HPV and cytology for cervical screening: A population-based evaluation in the United States

2021; Elsevier BV; Volume: 162; Issue: 3 Linguagem: Inglês

10.1016/j.ygyno.2021.06.029

ISSN

1095-6859

Autores

Jack Cuzick, Ruofei Du, Rachael Adcock, Walter Kinney, Nancy E. Joste, Ruth McDonald, Kevin English, Salina Torres, Debbie Saslow, Cosette M. Wheeler, Nancy E. Joste, Walter Kinney, Cosette M. Wheeler, Charles Wiggins, Michael Robertson, Ruth McDonald, Alan D. Waxman, Steven Jenison, Philip E. Castle, Vicki B. Benard, Stephanie C. Melkonian, Jean M. Howe, Debbie Saslow, Jane J. Kim, Mark H. Stoler, Jack Cuzick, Rebecca B. Perkins, Janice L. Gonzales, Salina Torres, Giovanna Rossi, Kevin English,

Tópico(s)

Global Cancer Incidence and Screening

Resumo

ObjectivesHuman papillomavirus (HPV) testing for cervical screening has been shown to increase the yield of precancerous disease and reduce the incidence of cervical cancer more than cytology alone. Here we document the state-wide uptake of co-testing with HPV and cytology in women aged 30–64 years as recommended by national and international bodies.MethodsRegistry-based study of all screening cytology and HPV tests in New Mexico from 2008 to 2019 among women aged 21–64 years, with a focus on cytology negative tests to distinguish co-testing from reflex HPV testing to triage equivocal or mildly abnormal cytology.ResultsA total of 1,704,055 cervical screening tests from 681,440 women aged 21–64 years in the state of New Mexico were identified. The proportion of screening tests which were co-tests rose from 5.6% in 2008 to 84.3% in 2019 among women aged 30–64 years with a marked change from the near exclusive use of the Hybrid Capture II HPV test, (a signal amplified test method) to the use of target amplified HPV tests. The largest increases were seen between 2013 and 2015, reflecting the introduction and adoption of new clinical guidelines. Increases in co-testing were also seen in younger women.ConclusionsCo-testing is now well established in women aged 30–64 years, but smaller increases have also been seen at younger ages, although this is not currently recommended. The impact of co-testing on cervical disease outcomes and number of colposcopies and biopsies in routine population settings remain important, especially in young women.

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