...
首页> 外文期刊>Journal of Cytology >Evaluation of p16/Ki-67 Dual Staining Compared with HPV Genotyping in Anal Cytology with Diagnosis of ASC-US for Detection of High-Grade Anal Intraepithelial Lesions
【24h】

Evaluation of p16/Ki-67 Dual Staining Compared with HPV Genotyping in Anal Cytology with Diagnosis of ASC-US for Detection of High-Grade Anal Intraepithelial Lesions

机译:对P16 / KI-67双染色的评价与肛门细胞学中的HPV基因分型与ASC-US诊断检测高等级肛门上皮内病变

获取原文
获取原文并翻译 | 示例
           

摘要

Introduction: Human Papillomavirus (HPV) infection is the main risk factor for anogenital cancer. The objective of this study was to compare p16/Ki-67 dual staining to HPV genotyping in anal cytology samples with an atypical squamous cell of undetermined significance (ASC-US) for the identification of high-grade squamous intraepithelial lesion (HSIL). Methods: Anal cytology samples with an ASC-US result (n = 111) were collected from patients of a university hospital (Lyon, France) from 2014 to 2015. Cases with remaining squamous cells (n = 82) were stained using p16/Ki-67 dual staining (CINtec-Plus kit) and analyzed for HPV screening (CLART2-PCR kit) using a composite endpoint of biopsy and cytology results on follow-up specimens. Results: Detection of HSIL on follow-up specimens (5/22 biopsies; 1/29 cytology samples) was obtained in two out of six cases with p16/Ki-17 versus. five out of six with HPV genotyping alone. Sensitivity and specificity to detect HSIL for p16/Ki-67 was 33% (95% confidence interval [CI] [4; 77]) and 49% (95% CI [34; 64]) versus. 83% (95% CI [36; 99.6]) and 13% (95% CI [5; 27]) for HPV genotyping. Conclusion: Herein, HPV genotyping was more sensitive but less specific than p16/Ki-67 staining for the detection of subsequent HSIL in ASC-US anal cytology. A larger study is required to evaluate the combination of these biomarkers for triage.
机译:介绍:人乳头瘤病毒(HPV)感染是生物癌症的主要风险因素。本研究的目的是将P16 / KI-67双染色与肛门细胞学样本中的HPV基因分型进行了非典型鳞状细胞(ASC-US),用于鉴定高级鳞状上皮内皮病变(HSIL)。方法:从2014年至2015年从大学医院(Lyon,法国里昂)的患者中收集具有ASC-US结果(N = 111)的肛性细胞学样本。使用p16 / ki染色剩余鳞状细胞(n = 82)的病例-67双染色(Cintec-Plus套件),并使用活组织检查的复合终点分析HPV筛选(CLART2-PCR试剂盒)对随访标本的复合终点。结果:在六种情况下,在P16 / Ki-17与六种情况下检测后续样本上的HSIL(5/22活检; 1/29细胞学样本)。单独使用HPV基因分型五分之一。检测P16 / KI-67的HSIL的敏感性和特异性为33%(95%置信区间[CI] [4; 4; 77])和49%(95%CI [34; 64])与。 83%(95%CI [36; 99.6])和HPV基因分型的13%(95%CI [5; 5; 27])。结论:本文,HPV基因分型更敏感但比P16 / Ki-67染色更敏感,用于检测ASC-US肛门细胞学的后续HSIL。需要更大的研究来评估这些生物标志物进行分类的组合。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号