Department of Diagnostic Imaging and Nuclear Medicine, Kyoto University Hospital, 54 Shogoin-Kawaharacho, Sakyo-ku, Kyoto City, Kyoto, 606-8507, Japan.
Department of Medical Oncology, School of Medicine, Fukushima Medical University, 1 Hikarigaoka, Fukushima City, Fukushima, 960-1295, Japan.
Breast Cancer Res Treat. 2018 Jun;169(3):437-446. doi: 10.1007/s10549-018-4711-4. Epub 2018 Feb 8.
Premenopausal physiologic steroid levels change cyclically, in contrast to steady state low levels seen in postmenopausal patients. The purpose of this study was to evaluate whether F-fluorodeoxyglucose (F-FDG) uptake in breast cancer is influenced by physiological hormonal fluctuations.
A total of 160 primary invasive breast cancers from 155 females (54 premenopausal, 101 postmenopausal) who underwent F-FDG positron emission tomography/computed tomography before therapy were retrospectively analyzed. The maximal standardized uptake values (SUVmax) of tumors were compared with menstrual phases and menopausal status according to the following subgroups: 'luminal A-like,' 'luminal B-like,' and 'non-luminal.' Additionally, the effect of estradiol (E2) on F-FDG uptake in breast cancer cells was evaluated in vitro.
Among premenopausal patients, SUVmax during the periovulatory-luteal phase was significantly higher than that during the follicular phase in luminal A-like tumors (n = 25, p = 0.004), while it did not differ between the follicular phase and the periovulatory-luteal phase in luminal B-like (n = 24) and non-luminal tumors (n = 7). Multiple regression analysis showed menstrual phase, tumor size, and Ki-67 index are independent predictors for SUVmax in premenopausal luminal A-like tumors. There were no significant differences in SUVmax between pre- and postmenopausal patients in any of the subgroups. In in vitro studies, uptake in estrogen receptor-positive cells was significantly augmented when E2 concentration was increased from 0.01 to ≥ 1 nM.
Our data suggest that F-FDG uptake may be impacted by physiological hormonal fluctuations during menstrual cycle in luminal A-like cancers, and that E2 could be partly responsible for these events.
与绝经后患者所见的稳定低水平相比,绝经前生理性甾体激素水平呈周期性变化。本研究旨在评估氟-18-氟代脱氧葡萄糖(F-FDG)摄取是否受生理激素波动的影响。
回顾性分析了 155 例女性(54 例绝经前,101 例绝经后)160 例原发性浸润性乳腺癌患者,这些患者在治疗前均接受了 F-FDG 正电子发射断层扫描/计算机断层扫描。根据以下亚组(“管腔 A 样”、“管腔 B 样”和“非管腔”)比较肿瘤的最大标准化摄取值(SUVmax)与月经周期和绝经状态的关系。此外,还在体外评估了雌二醇(E2)对乳腺癌细胞 F-FDG 摄取的影响。
在绝经前患者中,管腔 A 样肿瘤在排卵-黄体期的 SUVmax 明显高于卵泡期(n=25,p=0.004),而管腔 B 样(n=24)和非管腔肿瘤(n=7)的卵泡期和排卵-黄体期之间的 SUVmax 无差异。多因素回归分析显示,月经周期、肿瘤大小和 Ki-67 指数是绝经前管腔 A 样肿瘤 SUVmax 的独立预测因子。在任何亚组中,绝经前和绝经后患者的 SUVmax 均无显著差异。在体外研究中,当 E2 浓度从 0.01 增加到≥1 nM 时,雌激素受体阳性细胞的摄取显著增加。
我们的数据表明,F-FDG 摄取可能受到月经周期中管腔 A 样癌生理激素波动的影响,而 E2 可能是这些事件的部分原因。