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Prognostic value of p16-INK4A protein in women with negative or CIN1 histology result: a follow-up study.

Authors :
Pacchiarotti A
Ferrari F
Bellardini P
Chini F
Collina G
Dalla Palma P
Ghiringhello B
Maccallini V
Musolino F
Negri G
Pisa R
Sabatucci I
Giorgi Rossi P
Source :
International journal of cancer [Int J Cancer] 2014 Feb 15; Vol. 134 (4), pp. 897-904. Date of Electronic Publication: 2013 Aug 29.
Publication Year :
2014

Abstract

P16-INK4A overexpression has been proposed as a prognostic marker to manage the follow up of women with positive cytology and/or HPV test but without high-grade cervical intraepithelial neoplasia (CIN2+). This study measures the relative risk (RR) of CIN2+ of p16 positive versus negative in these women. All the women referred to colposcopy from October 2008 to September 2010 with negative or CIN1 colposcopy-guided biopsy were included in the study; women surgically treated or having a CIN2-3 were excluded. All baseline biopsies were dyed with hematoxylin and eosin and p16. Women were followed up according to screening protocols, with cytology or colposcopy at 6 or 12 months. CIN2/3 RRs and 95% confidence intervals (95%CI) were computed. Of 442 eligible women, 369 (83.5%) had at least one follow-up episode. At baseline, 113 (30.6%) were CIN1, 248 (67.2%) negative, and 8 (2.2%) inadequate histology; 293 (79.4%) were p16-negative, 64 (17.3%) p16 positive and 12 (3.2%) not valid. During follow up, we found ten CIN2 and three CIN3; of these, six were p16 positive (sensitivity 46%, 95% CI 19-75). The absolute risk among p16 positives was 9.4/100 compared to 1.7/100 of the p16 negatives (RR 5.5; 95% CI 1.7-17.4). The risk was also higher for CIN1 than for histologically negative women (RR 4.4; 95% CI 1.3-14.3). The RR for p16 in CIN1 did not change (RR 5.2; 95% CI 0.6-47.5). P16 overexpression is a good candidate for modulating follow-up intensity after a negative colposcopy but is limited by its low prospective sensitivity.<br /> (© 2013 UICC.)

Details

Language :
English
ISSN :
1097-0215
Volume :
134
Issue :
4
Database :
MEDLINE
Journal :
International journal of cancer
Publication Type :
Academic Journal
Accession number :
23913416
Full Text :
https://doi.org/10.1002/ijc.28407