Department of Breast and Endocrine Surgery, Okayama University Hospital, 2-5-1 Shikata-cho, Kita-ku, Okayama, 700-8558, Japan.
Department of Breast Oncology, Gunma Prefectural Cancer Center, Gunma, Japan.
Breast Cancer. 2020 Sep;27(5):973-981. doi: 10.1007/s12282-020-01095-y. Epub 2020 May 11.
Second-line endocrine therapy (ET) for estrogen receptor (ER)-positive and human epidermal growth factor 2 (HER2)-negative metastatic breast cancer (MBC) is offered based on the response to first-line ET. However, no clinical trials have evaluated the efficacy and safety of secondary ETs in patients with poor responses to initial ET. This study evaluated the efficacy of second-line ET in ER-positive and HER2-negative postmenopausal MBC patients with low or very low sensitivity to initial ET.
This multicenter prospective observational cohort study evaluated the response of 49 patients to second-line ETs in postmenopausal MBC patients with low or very low sensitivity to initial ET. The primary endpoint was the clinical benefit rate (CBR) for 24 weeks.
Of the 49 patients assessed, 40 (82%) received fulvestrant in the second line, 5 (10%) received selective estrogen receptor modulators, 3 (6%) received aromatase inhibitors (AIs) alone, and 1 received everolimus with a steroidal AI. The overall CBR was 44.9% [90% confidence interval (CI): 34.6-57.6, p = 0.009]; CBR demonstrated similar significance across the progesterone receptor-positive (n = 39, 51.3%, 90% CI: 39.6-65.2, p = 0.002), very low sensitivity (n = 17, 58.8%, 90% CI: 42.0-78.8, p = 0.003), and non-visceral metastases (n = 25, 48.0%, 90% CI: 34.1-65.9, p = 0.018) groups. The median progression-free survival was 7.1 months (95% CI: 5.6-10.6).
Second-line ET might be a viable treatment option for postmenopausal patients with MBC with low and very low sensitivity to initial ET. Future studies based on larger and independent cohorts are needed to validate these findings.
对于雌激素受体(ER)阳性和人表皮生长因子 2(HER2)阴性转移性乳腺癌(MBC)患者,二线内分泌治疗(ET)是基于一线 ET 的反应而提供的。然而,尚无临床试验评估初始 ET 反应不佳的患者接受二线 ET 的疗效和安全性。本研究评估了二线 ET 在初始 ET 敏感性低或非常低的 ER 阳性和 HER2 阴性绝经后 MBC 患者中的疗效。
这项多中心前瞻性观察性队列研究评估了 49 例初始 ET 敏感性低或非常低的绝经后 MBC 患者二线 ET 的反应。主要终点为 24 周的临床获益率(CBR)。
在评估的 49 例患者中,40 例(82%)在二线治疗中接受氟维司群,5 例(10%)接受选择性雌激素受体调节剂,3 例(6%)单独接受芳香化酶抑制剂(AIs),1 例接受依维莫司联合甾体 AI。总 CBR 为 44.9%[90%置信区间(CI):34.6-57.6,p=0.009];孕激素受体阳性(n=39,51.3%,90%CI:39.6-65.2,p=0.002)、非常低敏感性(n=17,58.8%,90%CI:42.0-78.8,p=0.003)和非内脏转移(n=25,48.0%,90%CI:34.1-65.9,p=0.018)患者的 CBR 具有相似的显著意义。中位无进展生存期为 7.1 个月(95%CI:5.6-10.6)。
对于初始 ET 敏感性低或非常低的绝经后 MBC 患者,二线 ET 可能是一种可行的治疗选择。需要基于更大和独立队列的进一步研究来验证这些发现。