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J Low Genit Tract Dis. 2014 Jul;18(3):203-9. doi: 10.1097/LGT.0b013e3182a1772c.

Postcolposcopy management of women with histologically proven CIN 1: results from TOMBOLA.

Author information

1
1Gynaecological Oncology, University Hospital of Llandough, Wales; and 2University of Aberdeen, Aberdeen, United Kingdom; 3National Cancer Registry Ireland, Cork, Ireland; 4Aberdeen Royal Infirmary, Aberdeen, United Kingdom; 5Department of Epidemiology and Community Medicine, University of Ottawa, Ottawa, Canada; and 6Warwick Medical School, Coventry, United Kingdom.

Abstract

OBJECTIVES:

This study aimed to determine during 36 months of follow-up the (1) clinical outcomes and (2) influence of high-risk human papillomavirus (HPV) status on the risk of progression to cervical intraepithelial neoplasia 2+ (CIN 2+), among women with histologically proven CIN 1.

MATERIALS AND METHODS:

This is an ad hoc analysis of women with CIN 1 within TOMBOLA, a randomized trial of the management of women with low-grade cervical cytology. Women from the colposcopy arm with CIN 1 confirmed on punch biopsies and managed conservatively by cytology every 6 months in primary care were included. Sociodemographic data and a sample for HPV testing were collected at recruitment. Data on the sample women were extracted to calculate the cumulative incidence of CIN 2+ and the performance characteristics of the baseline HPV test. Detection of CIN 2 or worse (CIN 2+) during follow-up or at exit colposcopy was analyzed.

RESULTS:

A total of 171 women were included. Their median age was 29 years. Fifty-two percent were high-risk HPV positive, 17% were HPV-16 positive, and 11% were HPV-18 positive. Overall, 21 women (12%) developed CIN 2+, with a median time to detection of 25 months. Factors associated with progression to CIN 2+ were presence of HPV-18 (relative risk = 3.04; 95% CI = 1.09-8.44) and HPV-16 and/or HPV-18 at recruitment (relative risk = 3.98; 95% CI = 1.60-9.90). The sensitivity and specificity of a combined HPV-16/HPV-18 test for the detection of CIN 2+ during 3 years were 58% and 78%, respectively.

CONCLUSIONS:

Our results suggest that women with confirmed CIN 1 have low rates of progression to high-grade CIN within 3 years. Because the median time to progression was 25 months, conservative management could recommend the next repeat cytology at 2 years.

PMID:
24270198
DOI:
10.1097/LGT.0b013e3182a1772c
[Indexed for MEDLINE]

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