Menopausal Hormone Therapy, Hormone Receptor Status, and Lung Cancer in Women

被引:20
作者
Chlebowski, Rowan T. [1 ]
机构
[1] Harbor UCLA Med Ctr, Los Angeles Biomed Res Inst, Torrance, CA 90502 USA
基金
美国国家卫生研究院;
关键词
ESTROGEN PLUS PROGESTIN; HEALTHY POSTMENOPAUSAL WOMEN; REPLACEMENT THERAPY; REPRODUCTIVE FACTORS; SURVIVAL; RISK; BETA; EXPRESSION; SMOKING; ANGIOGENESIS;
D O I
10.1053/j.seminoncol.2009.10.008
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Gender differences in lung cancer incidence and outcome suggest a potential role for reproductive hormones. However, observational studies regarding menopausal hormone therapy use and lung cancer have given mixed results. Some have associated hormone therapy use with increased lung cancer risk, while others have shown no effect or found lower lung cancer risk in hormone therapy users. Against this background the Women's Health Initiative (WHO randomized controlled trial evaluating conjugated equine estrogen (CEE) and medroxyprogesterone acetate (MPA) in postmenopausal women identified an increase in malignancies in the hormone therapy group during the post intervention period. Post hoc analyses identified a statistically significant increase in deaths from lung cancer for women in the hormone group largely related to effects on non-small cell lung cancer (NSCLC). The NSCLCs were more commonly poorly differentiated and were diagnosed at a metastatic stage, suggesting a hormone effect on already established lung cancer growth. Ongoing preclinical and clinical analyses have identified estrogen receptors in the nucleus and cytoplasm of lung tissue and lung cancers. More recently, intriguing associations among estrogen receptor expression, lung cancer histology, clinical prognosis, and epidermal growth factor receptor (EGFR) mutations have been reported. The WHI clinical findings should be integrated into risk-benefit discussion with women considering combined hormone therapy use. In addition, the findings, together with ongoing studies evaluating estrogen receptor status and function, support further efforts to develop lung cancer intervention strategies targeting estrogen receptor expression. Semin Oncol 36:566-571 (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:566 / 571
页数:6
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