Department of Internal Medicine, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea
Department of Internal Medicine, Inha University College of Medicine, Incheon, Republic of Korea.
Oncologist. 2019 Aug;24(8):e653-e661. doi: 10.1634/theoncologist.2018-0370. Epub 2019 Jan 24.
Unlike tamoxifen, the relationship between aromatase inhibitor use in postmenopausal patients with breast cancer and nonalcoholic fatty liver disease (NAFLD) has not been delineated.
A retrospective analysis of 253 patients with early breast cancer without baseline NAFLD and treated with nonsteroidal aromatase inhibitors was performed. Among them, 220 patients were matched for sex, age, and menstruation status with healthy patients, and the prevalence of NAFLD was compared. NAFLD was determined by hepatic steatosis index in the absence of other known liver diseases. The presence of significant liver fibrosis in patients with NAFLD was determined noninvasively by AST-platelet ratio index, FIB-4 score, and NAFLD fibrosis score (NFS).
Postmenopausal patients with breast cancer undergoing treatment with aromatase inhibitors had higher prevalence of NAFLD independent of body mass index (BMI) and underlying diabetes mellitus (DM). Although the aromatase inhibitor group showed higher fibrotic burden by NFS, independent of BMI and DM, the proportion of advanced fibrosis did not show statistically significant differences between AI-treated patients and the healthy patients. Those with abnormal baseline fasting glucose levels are suggested to have increased risk of NAFLD development after aromatase inhibitor treatment. In addition, patients with NAFLD developed after aromatase inhibitor use had significantly lower disease-free survival than those without NAFLD, although there was no significant difference in overall survival.
Results of this study suggest that inhibition of estrogen synthesis in postmenopausal women undergoing treatment with aromatase inhibitors could increase the risk of NAFLD, which might have some influence on the prognosis of patients with breast cancer.
Unlike tamoxifen, the role of aromatase inhibitor treatment use in postmenopausal patients with breast cancer in development of fatty liver is not well known. In this propensity-matched cohort study, postmenopausal patients with breast cancer treated with aromatase inhibitors had increased risk of nonalcoholic fatty liver disease compared with healthy women after menopause, independent of obesity and diabetes mellitus. The results show possible adverse influence of the newly developed fatty liver on breast cancer disease-free survival and suggest a necessity for further validation. Fatty liver may need to be considered as an adverse event for aromatase inhibitor treatment.
与他莫昔芬不同,芳香化酶抑制剂在绝经后乳腺癌患者中的应用与非酒精性脂肪性肝病(NAFLD)之间的关系尚未明确。
对 253 例无基线非酒精性脂肪性肝病且接受非甾体类芳香化酶抑制剂治疗的早期乳腺癌患者进行回顾性分析。其中,220 例患者按性别、年龄和月经状态与健康患者相匹配,并比较了非酒精性脂肪性肝病的患病率。在没有其他已知肝病的情况下,通过肝脂肪变性指数来确定非酒精性脂肪性肝病。通过 AST-血小板比值指数、FIB-4 评分和 NAFLD 纤维化评分(NFS)来无创性地确定非酒精性脂肪性肝病患者中存在显著的肝纤维化。
接受芳香化酶抑制剂治疗的绝经后乳腺癌患者,不论体重指数(BMI)和潜在的糖尿病(DM)如何,NAFLD 的患病率均较高。尽管芳香化酶抑制剂组的 NFS 显示纤维化负担更高,但与 BMI 和 DM 无关,AI 治疗患者与健康患者之间的晚期纤维化比例并无统计学显著差异。基线空腹血糖水平异常者,提示在接受芳香化酶抑制剂治疗后发生非酒精性脂肪性肝病的风险增加。此外,与未发生非酒精性脂肪性肝病的患者相比,在接受芳香化酶抑制剂治疗后发生非酒精性脂肪性肝病的患者无病生存率显著降低,尽管总生存率无显著差异。
本研究结果表明,绝经后女性接受芳香化酶抑制剂治疗时抑制雌激素合成可能会增加非酒精性脂肪性肝病的风险,这可能对乳腺癌患者的预后产生一定影响。
与他莫昔芬不同,芳香化酶抑制剂在绝经后乳腺癌患者中的应用在脂肪性肝病的发展中的作用尚不清楚。在这项倾向匹配队列研究中,与绝经后健康女性相比,接受芳香化酶抑制剂治疗的绝经后乳腺癌患者发生非酒精性脂肪性肝病的风险增加,这与肥胖和糖尿病无关。结果表明,新发生的脂肪肝可能对乳腺癌无病生存率产生不利影响,并提示需要进一步验证。脂肪肝可能需要被视为芳香化酶抑制剂治疗的不良事件。