Title
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DOI
Article Type
Special Issue
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Evaluation of p16/Ki67 dual staining compared with high-risk HPV testing to assess liquid-based cytology with atypical squamous cells of unknown significance
1,Department of Obstetrics and Gynecology
2Department of Pathology, The Second Affiliated Hospital of Jiaxing Medical College, Jiaxing, Zhejiang Province, China
DOI: 10.12892/ejgo4277.2019 Vol.40,Issue 2,April 2019 pp.249-253
Accepted: 26 June 2017
Published: 10 April 2019
*Corresponding Author(s): F. Liu E-mail: jxliufang@hotmail.com
Objective: To compare the clinical performance of p16/Ki67 dual staining and high risk-human papilloma virus (HR-HPV) testing as an auxiliary monitoring index to triage atypical squamous cells of undetermined significance (ASCUS). Materials and Methods: Fifty-four patients diagnosed with ASCUS by liquid-based cytology were inspected by colposcopy-guided biopsy and cervical histopathological examination. The cytological samples were tested for HR-HPV with Cervista HPV assays, and the cell morphology was evaluated with dual staining using the CINtec PLUS kit. ROC curves were used to evaluate the diagnostic value of p16/Ki67 dual staining and HR-HPV assays to detect underlying CIN2+ in ASCUS patients. The kappa value assessed the reliability of p16/Ki67 dual staining and HR-HPV, and the diagnostic advantages of the two tests were analyzed using logistic regression analysis. Results: Twenty-two of the 54 ASCUS cases were diagnosed as CIN2+ by histopathology. The area under the ROC curve was 0.776 (95%CI 0.647-0.904) and 0.689 (95%CI 0.548-0.830) for CIN2+ detection using p16/Ki67 dual-staining cytology and HR-HPV, respectively. P16/Ki67 dual staining demonstrated a sensitivity and negative predictive value similar to that of HR-HPV for detecting underlying CIN2+ in ASCUS (86.36% vs. 90.91%, 88.00% vs. 88.24%). There was a certain degree of concordance between the p16/Ki67 dual staining cytological assay and the HR-HPV test (kappa = 0.315, p = 0.015). The accuracy of CIN2+ diagnosis using p16/Ki67 dual staining cytology was higher than that of HR-HPV (OR=11.025 vs. OR=6.026, p = 0.001). Conclusions: P16/Ki67 dual staining and HR-HPV can be used as an auxiliary monitoring index to triage ASCUS. The diagnostic value of p16/Ki67 dual staining was superior to that of HR-HPV for detecting underlying CIN2+ in ASCUS.
Human papillomavirus (HPV); Atypical squamous cell of undetermined significance(ASCUS); P16/Ki67 dual staining; Cervical intraepithelial neoplasia (CIN)
F. Liu,D.H. Hu,M.J. Fei,Y.F. Zhang,B. Wang,C.Y. Wang,K. Huang. Evaluation of p16/Ki67 dual staining compared with high-risk HPV testing to assess liquid-based cytology with atypical squamous cells of unknown significance. European Journal of Gynaecological Oncology. 2019. 40(2);249-253.
[1] Jones H.W. 3rd.: “Clinical treatment of women with atypical squamous cells of undetermined significance or atypical glandular cells of undetermined significance cervical cytology”. Clin. Obstet. Gynecol., 2000, 43, 381.
[2] Li N., Franceschi S., Howell-Jones R., Snijders P.J., Clifford G.M.: “Human papillomavirus type distribution in 30,848 invasive cervical cancers worldwide: Variation by geographical region, histological type and year of publication”. Int. J. Cancer., 2011, 128, 927.
[3] Fakhreldin M., Elmasry K.: “Improving the performance of reflex Human Papilloma Virus (HPV) testing in triaging women with atypical squamous cells of undetermined significance (ASCUS): A restrospective study in a tertiary hospital in United Arab Emirates (UAE)”. Vaccine, 2016, 34, 823.
[4] Karimi-Zarchi M., Tabatabaie A., Dehghani-Firoozabadi A., Shamsi F., Baghianimoghaddam M., Dargahi M., et al.: “The Most Common Type of HPV in Women with Atypical Squamous Cell of Undetermined Significance (ASCUS) in Pap Smear in Iran-Yazd”. Int. J. Biomed. Sci., 2015, 11, 173.
[5] Cuzick J., Clavel C., Petry K.U., Meijer C.J., Hoyer H., Ratnam S., et al.: “Overview of the European and North American studies on HPV testing in primary cervical cancer screening”. Int. J. Cancer, 2006, 119, 1095.
[6] Alonso I., Torne A., Puig-Tintore L.M., Esteve R., Quinto L., Campo E., et al.: “Pre- and post-conization high-risk HPV testing predicts residual/recurrent disease in patients treated for CIN 2-3”. Gynecol. Oncol., 2006, 103, 631.
[7] Solomon D., Schiffman M., Tarone R.: “Comparison of three management strategies for patients with atypical squamous cells of undetermined significance: baseline results from a randomized trial”. J. Natl. Cancer, 2001, 93, 293.
[8] Cuzick J., Mayrand M.H., Ronco G., Snijders P., Wardle J.: “Chapter 10: New dimensions in cervical cancer screening”. Vaccine, 2006, 24, S3/90.
[9] Wentzensen N., Bergeron C., Cas F., Vinokurova S., von Knebel Doeberitz M.: “Triage of women with ASCUS and LSIL cytology: use of qualitative assessment of p16INK4a positive cells to identify patients with high-grade cervical intraepithelial neoplasia”. Cancer, 2007, 111, 58.
[10] Khan A.M., Singer A.: “Biomarkers in cervical precancer management: the new frontiers”. Future. Oncol., 2008, 4, 515.
[11] Petry K.U., Schmidt D., Scherbring S., Luyten A., Reinecke-Luthge A., Bergeron C., et al.: “Triaging Pap cytology negative, HPV positive cervical cancer screening results with p16/Ki-67 Dual-stained cytology”. Gynecol. Oncol., 2011, 121, 505.
[12] Ikenberg H., Bergeron C., Schmidt D., Griesser H., Alameda F., Angeloni C., et al.: “Screening for cervical cancer precursors with p16/Ki-67 dual-stained cytology: results of the PALMS study”. J. Natl. Cancer. Inst., 2013, 105, 1550.
[13] Uijterwaal M.H., Polman N.J., Witte B.I., van Kemenade F.J., Rijkaart D., Berkhof J., et al.: “Triaging HPV-positive women with normal cytology by p16/Ki-67 dual-stained cytology testing: baseline and longitudinal data”. Int. J. Cancer, 2015, 136, 2361.
[14] Wentzensen N., Fetterman B., Castle P.E., Schiffman M., Wood S.N., Stiemerling E., et al.: “p16/Ki-67 Dual Stain Cytology for Detection of Cervical Precancer in HPV-Positive Women”. J. Natl. Cancer Inst., 2015, 107, djv257.
[15] Wentzensen N., Schwartz L., Zuna R.E., Smith K., Mathews C., Gold M.A., et al.: “Performance of p16/Ki-67 immunostaining to detect cervical cancer precursors in a colposcopy referral population”. Clin. Cancer. Res., 2012, 18, 4154.
[16] Einstein M.H., Martens M.G., Garcia F.A., Ferris D.G., Mitchell A.L., Day S.P. et al.: “Clinical validation of the Cervista HPV HR and 16/18 genotyping tests for use in women with ASC-US cytology”. Gynecol. Oncol., 2010, 118, 116.
[17] Cuschieri K., Wentzensen N.: “Human papillomavirus mRNA and p16 detection as biomarkers for the improved diagnosis of cervical neoplasia”. Cancer. Epidemiol. Biomarkers. Prev., 2008, 17, 2536.
[18] Tsoumpou I., Arbyn M., Kyrgiou M., Wentzensen N., Koliopoulos G., Martin-Hirsch P., et al.: “p16(INK4a) immunostaining in cytological and histological specimens from the uterine cervix: a systematic review and meta-analysis”. Cancer Treat. Rev., 2009, 35, 210.
[19] Kanthiya K., Khunnarong J., Tangjitgamol S., Puripat N. Tanvanich S.: “Expression of the p16 and Ki67 in Cervical Squamous Intraepithelial Lesions and Cancer”. Asian Pac. J. Cancer Prev., 2016, 17, 3201.
[20] Schmidt D., Bergeron C., Denton K.J. Ridder R.: “p16/ki-67 dualstain cytology in the triage of ASCUS and LSIL papanicolaou cytology: results from the European equivocal or mildly abnormal Papanicolaou cytology study”. Cancer Cytopathol., 2011, 119, 158.
[21] Arbyn M., Ronco G., Meijer C.J. Naucler P.: “Trials comparing cytology with human papillomavirus screening”. Lancet. Oncol., 2009, 10, 935.
[22] Mayrand M.H., Duarte-Franco E., Rodrigues I., Walter S.D., Hanley J., Ferenczy A., et al.: “Human papillomavirus DNA versus Papanicolaou screening tests for cervical cancer”. N. Engl. J. Med., 2007, 357, 1579.
[23] Wright T.C. Jr., Schiffman M., Solomon D., Cox J.T., Garcia F., Goldie S., et al.: “Interim guidance for the use of human papillomavirus DNA testing as an adjunct to cervical cytology for screening”. Obstet. Gynecol., 2004, 103, 304.
[24] Ekalaksananan T., Pientong C., Sriamporn S., Kongyingyoes B., Pengsa P., Kleebkaow P., et al.: “Usefulness of combining testing for p16 protein and human papillomavirus (HPV) in cervical carcinoma screening”. Gynecol. Oncol., 2006, 103, 62.
[25] Waldstrom M., Christensen R.K., Ornskov D.: “Evaluation of p16(INK4a)/Ki-67 dual stain in comparison with an mRNA human papillomavirus test on liquid-based cytology samples with low-grade squamous intraepithelial lesion”. Cancer Cytopathol., 2013, 121, 136.
[26] Dona M.G., Vocaturo A., Giuliani M., Ronchetti L., Rollo F., Pescarmona E., et al.: “p16/Ki-67 dual staining in cervico-vaginal cytology: correlation with histology, Human Papillomavirus detection and genotyping in women undergoing colposcopy”. Gynecol. Oncol., 2012, 126, 198.
[27] Denton K.J., Bergeron C., Klement P., Trunk M.J., Keller T., Ridder R.: “The sensitivity and specificity of p16(INK4a) cytology vs HPV testing for detecting high-grade cervical disease in the triage of ASC-US and LSIL pap cytology results”. Am. J. Clin. Pathol., 2010, 134, 12.
[28] Samarawardana P., Dehn D.L., Singh M., Franquemont D., Thompson C., Gaido L., et al.: “p16(INK4a) is superior to high-risk human papillomavirus testing in cervical cytology for the prediction of underlying high-grade dysplasia”. Cancer Cytopathol., 2010, 118, 146.
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