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Age‐specific 3‐year cumulative risk of cervical cancer and high‐grade dysplasia on biopsy in 9434 women who underwent HPV cytology cotesting
Author(s) -
Ge Yimin,
Christensen Paul A.,
Luna Eric,
Armylagos Donna,
Xu Jiaqiong,
Hsu Jim W.,
Zhou Haijun,
Schwartz Mary R.,
Mody Dina R.
Publication year - 2019
Publication title -
cancer cytopathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.29
H-Index - 57
eISSN - 1934-6638
pISSN - 1934-662X
DOI - 10.1002/cncy.22192
Subject(s) - medicine , dysplasia , biopsy , cytology , cumulative risk , cancer , gynecology , obstetrics , pathology
Background High‐risk human papillomavirus (HPV)–Papanicolaou (Pap) cotesting is recommended for cervical cancer screening in women aged ≥30 years. The current study analyzed the effectiveness of cotesting on risk management in different age groups. Methods A retrospective review of a 5‐year cytology database identified 9434 women with HPV‐Pap cotesting and follow‐up cervical biopsy. The 3‐year cumulative risk of developing high‐grade cervical lesions (≥high‐grade squamous intraepithelial lesion [HSIL]) was analyzed using age stratification. Results The 3‐year cumulative risk of developing ≥HSIL was found to be significantly different in women with baseline cotesting HPV‐positive and Pap‐positive results (HPV+/Pap+; defined as ≥atypical squamous cells of undetermined significance), HPV+ and Pap‐negative results, and HPV‐negative and Pap+ results at 19.2%, 7.9%, and 3.1%, respectively ( P  < .001). The risk of ≥HSIL peaked at ages 30 to 39 years and significantly decreased at ages 50 to 59 years (16.6% vs 6.7%; P  < .001). Women aged <30 years shared a high risk similar to that of women aged 30 to 39 years (17.3% vs 16.6%; P  = .52), and risk stratification by cotesting was found to be equally effective in the younger age group (HPV+ and Pap+: 19.6%; HPV+ and Pap‐negative: 7.2%; and HPV‐negative and Pap+: 4.4% [ P  < .001]). Conclusions High‐risk HPV–Pap cotesting appears to be extremely sensitive for the prediction of the risk of developing ≥HSIL and is an effective tool for risk stratification. In the current study, the 3‐year cumulative risk of developing ≥HSIL varied significantly with age, with the highest risk noted among women aged <40 years and the lowest risk observed in women aged 50 to 59 years. Pap testing significantly impacted risk stratification in the HPV+ positive group, especially in women aged <60 years. Women aged <30 years were found to have a risk profile and cotesting efficacy similar to those of women aged 30 to 39 years. Modification of the current recommendation to offer cotesting to women aged ≥30 years might be considered to include those patients aged <30 years.

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