p16INK4a immunostaining in cytological and histological specimens from the uterine cervix: A systematic review and meta-analysis

被引:226
|
作者
Tsoumpou, I. [1 ]
Arbyn, M. [2 ]
Kyrgiou, M. [3 ]
Wentzensen, N. [4 ]
Koliopoulos, G. [5 ]
Martin-Hirsch, P. [6 ]
Malamou-Mitsi, V. [7 ]
Paraskevaidis, E. [5 ]
机构
[1] CMMC Univ Hosp, St Marys Hosp, Dept Obstet & Gynaecol, Manchester M13 0JH, Lancs, England
[2] Sci Inst Publ Hlth, B-1050 Brussels, Belgium
[3] W Middlesex Univ Hosp, Dept Obstet & Gynaecol, London, England
[4] Natl Canc Inst, Div Canc Epidemiol & Genet, NIH, DHHS, Bethesda, MD USA
[5] Univ Ioannina, Sch Med, Dept Obstet & Gynaecol, GR-45110 Ioannina, Greece
[6] Cent Lancashire Teaching Hosp, Dept Obstet & Gynaecol, Preston, Lancs, England
[7] Univ Ioannina, Sch Med, Dept Pathol, GR-45110 Ioannina, Greece
关键词
Cancer; Dysplasia; SIL; CIN; Cervix; p16; Cyclin-dependent kinase; LIQUID-BASED CYTOLOGY; HIGH-RISK HPV; IN-SITU HYBRIDIZATION; IMMUNOHISTOCHEMICAL P16 EXPRESSION; GRADE INTRAEPITHELIAL NEOPLASIA; HUMAN-PAPILLOMAVIRUS INFECTION; ATYPICAL SQUAMOUS-CELLS; EQUIVOCAL PAP-SMEARS; FOLLOW-UP; GLANDULAR LESIONS;
D O I
10.1016/j.ctrv.2008.10.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: P16(INK4a) is a biomarker for transforming HPV infections that could act as an adjunct to current cytological and histological assessment of cervical smears and biopsies, allowing the identification of those women with ambiguous results that require referral to colposcopy and potentially treatment. Material and methods: We conducted a systematic review of all studies that evaluated the use of p16(INK4a) in cytological or histological specimens from the uterine cervix. We also estimated the mean proportion of samples that were positive for p16(INK4a) in cytology and histology, stratified by the grade of the lesion. Results: Sixty-one studies were included. The proportion of cervical smears overexpressing p16(INK4a) increased with the severity of cytological abnormality. Among normal smears, only 12% (95% CI: 7-17%) were positive for the biomarker compared to 45% of ASCUS and LSIL (95% CI: 35-54% and 37-57%, respectively) and 89% of HSIL smears (95% CI: 84-95%). Similarly, in histology only 2% of normal biopsies (95% CI: 0.4-30%) and 38% of CIN1 (95% CI: 23-53%) showed diffuse staining for p16(INK4a) compared to 68% of CIN2 (95% CI: 44-92%)and 82% of CIN3 (95% CI: 72-92%). Conclusion: Although there is good evidence that p16(INK4a) immunostaining correlates with the severity of cytological/histological abnormalities, the reproducibility is limited due to insufficiently standardized interpretation of the immunostaining. Therefore, a consensus needs to be reached regarding the evaluation of p16(INK4a) staining and the biomarker needs to be assessed in various clinical settings addressing specific clinical questions. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:210 / 220
页数:11
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