Evaluation of p16INK4a/Ki-67 dual stain in comparison with an mRNA human papillomavirus test on liquid-based cytology samples with low-grade squamous intraepithelial lesion

被引:61
作者
Waldstrom, Marianne [1 ,2 ]
Christensen, Rikke Kolby [1 ]
Ornskov, Dorthe [3 ]
机构
[1] Vejle Hosp, Dept Clin Pathol, DK-7100 Vejle, Denmark
[2] Univ So Denmark, Inst Reg Hlth Serv Res, Odense, Denmark
[3] Vejle Hosp, Dept Clin Microbiol, DK-7100 Vejle, Denmark
关键词
APTIMA human papillomavirus (HPV) assay; CINtec PLUS test; dual immunocytochemical stain; low-grade squamous intraepithelial lesion (LSIL); triage; FOLLOW-UP; HPV DNA; WOMEN; P16(INK4A); TRIAGE; ASCUS; PERFORMANCE; PREDICTORS; NEOPLASIA; RISK;
D O I
10.1002/cncy.21233
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: The objective of the current study was to investigate the clinical performance of detecting high-grade lesions with the CINtec PLUS p16INK4a/Ki-67 dual stain and the APTIMA human papillomavirus (HPV) Assay in a cohort of women with low-grade squamous intraepithelial lesion (LSIL) cytology. The authors also assessed the reproducibility of the evaluation of immunocytochemical staining. METHODS: The 2 tests were performed on liquid-based residual material from 469 women with LSILs. The samples had at least 5 years of follow-up and the gold standard used was high-grade cervical intraepithelial neoplasia (CIN2+/CIN3+) proven on histology. RESULTS: Approximately 69% of all the women included in the study had a positive test for HPV mRNA and 56% was positive for the dual stain. The 2 tests demonstrated high sensitivities. When examining the specificities, the APTIMA HPV Assay performed with significantly lower values than the CINtec PLUS test. For patients with CIN2+, the APTIMA HPV Assay had a specificity of 36.1% versus 51.3% for the CINtec PLUS test, and for women with CIN3+, the specificity was 33.8% versus 48.2%, respectively. The difference was even more pronounced when analyzing women aged < 30 years separately. The kappa values between the 3 observers in scoring the dual stain ranged from 0.43 to 0.49 and improved in a second evaluation round to values ranging from 0.50 to 0.66. CONCLUSIONS: The CINtec PLUS p16INK4a/Ki-67 dual-staining test in LSIL cytology samples demonstrated high sensitivity that was similar to that of the APTIMA HPV Assay in the detection of underlying high-grade disease but with enhanced specificity, especially among women aged < 30 years. The kappa value for the evaluation of the CINtec PLUS dual-staining test was moderate but could be improved through training. Cancer (Cancer Cytopathol) 2013. (c) 2012 American Cancer Society.
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页码:136 / 145
页数:10
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