期刊
GYNECOLOGIC ONCOLOGY
卷 141, 期 2, 页码 312-317出版社
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ygyno.2016.03.006
关键词
Endometrial cancer; Biomarker; Estrogen receptor alpha; ESR1; Lymph node metastasis; Survival
资金
- American Cancer Society [IRG-67-003-50]
- Pelotonia Fellowship Program
Background We sought to validate the prognostic significance of estrogen receptor alpha (ER alpha) expression and to investigate the relationship between ESR1 mutation status and outcomes in a large cohort of patients with endometrial cancer. We also investigated the predictive value of ER alpha for lymph node involvement in a large surgically staged cohort. Methods. A tumor microarray (TMA) was constructed including only pure endometrioid adenocarcinomas, stained with ER50 monoclonal antibody, and assessed using digital image analysis. For mutation analysis, somatic DNA. was extracted and sequenced for ESR1 gene hotspot regions. Differences in patient and tumor characteristics, recurrence and survival between ER alpha positive and negative, mutated and wild-type tumors were evaluated. Results. Sixty. (18.6%) tumors were negative for ER alpha. Absence of ER alpha was significantly associated with stage and grade, but not with disease-free or overall survival. ER alpha was a strong predictor of lymph node involvement (RR: 2.37, 95% CI: 1.12-5.02). Nineteen of 1034 tumors (1.8%) had an ESR1 hotspot mutation; twelve in hotspot 537Y, four in 538D and three in 536 L.,Patients with an ESR1 mutation had a significantly lower BMI, but were comparable in age, stage-and grade, and progression-free survival. Conclusion. Patients with ER alpha negative endometrioid endometrial cancer are more often diagnosed with higher grade and advanced stage disease. Lymph node involvement is more common with lack of ER alpha expression, and may be able to help triage which patients should undergo lymphadenectomy. Mutations in ESR1 might explain why some low risk women with low BMI develop endometrial cancer. (C) 2016 Elsevier Inc. All rights reserved.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据