Pathologic Scoring of PTEN Immunohistochemistry in Endometrial Carcinoma is Highly Reproducible

被引:67
作者
Garg, Karuna [1 ]
Broaddus, Russell R. [4 ]
Soslow, Robert A. [1 ]
Urbauer, Diana L. [5 ]
Levine, Douglas A. [2 ]
Djordjevic, Bojana [3 ,4 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Pathol, New York, NY 10065 USA
[2] Mem Sloan Kettering Canc Ctr, Dept Surg, New York, NY 10065 USA
[3] Univ Ottawa, Ottawa Hosp, Dept Pathol & Lab Med, Ottawa, ON K1N 6N5, Canada
[4] Univ Texas MD Anderson Canc Ctr, Dept Pathol, Houston, TX USA
[5] Univ Texas MD Anderson Canc Ctr, Dept Epidemiol & Biostat, Houston, TX USA
关键词
Endometrial carcinoma; PI3K pathway; PTEN immunohistochemistry; TISSUE MICROARRAY; PTEN(+/-) MICE; CANCER; MUTATIONS; BREAST; EXPRESSION; SENSITIVITY; PRECANCERS; ANTIBODIES; INHIBITORS;
D O I
10.1097/PGP.0b013e3182230d00
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Endometrial carcinomas show frequent PTEN-PI3K pathway abnormalities, and there are currently multiple trials focused on PI3K pathway inhibitors in patients with endometrial carcinoma. PTEN immunohistochemistry may help to select patients with potential for response to targeted therapy, making it important to develop and validate this stain in formalin-fixed, paraffin-embedded tissue. Immunohistochemistry for PTEN was performed and scored independently on 118 cases of endometrial carcinomas from 2 cancer centers using monoclonal DAKO 6H2.1 antibody. Cases were scored as positive, negative, or heterogeneous; reproducibility of PTEN staining and interpretation was assessed. Overall interobserver agreement was good (weighted kappa = 0.80), with 82% concordance, similar for nonendometrioid (81%) and endometrioid carcinomas (85%). Twenty-one of 118 cases showed discrepant results (17%) that resulted from differences in interpretation and not staining. Our study shows that evaluation of PTEN loss by immunohistochemistry is highly reproducible with the application of standard immunohistochemical techniques and simple scoring criteria.
引用
收藏
页码:48 / 56
页数:9
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