Breast Oncology, Aichi Cancer Center Hospital, 1-1 Kanokoden, Chikusa-ku, Nagoya, 464-8681, Japan.
Kumamoto University Hospital, 1-1-1 Honjo, Chuo-ku, Kumamoto, 860-8556, Japan.
Breast Cancer Res Treat. 2023 Jun;199(2):231-241. doi: 10.1007/s10549-023-06874-7. Epub 2023 Mar 22.
Neoadjuvant endocrine therapy (NET) is a treatment option for estrogen receptor-positive (ER+) postmenopausal early breast cancer (EBC). This phase III trial evaluated the prognosis of EBC patients treated with/without chemotherapy (CT) following NET.
ER+/HER2-, T1c-2, and clinically node-negative EBC patients were enrolled in 2008-2013 and treated with endocrine therapy (ET) in weeks 24-28. All patients, excluding those with progressive disease (PD) during NET or ≥ 4 positive lymph nodes after surgery, were randomized to ET for 4.5-5 years with/without CT. The primary endpoint was disease-free survival (DFS). Secondary endpoints included distant DFS (DDFS), overall survival (OS), and DFS/DDFS/OS according to clinical response to NET.
Of 904 patients, 669 were randomized to CT+ET (n = 333) or ET alone (n = 336). The median follow-up was 7.8 years. DFS (CT+ET, 47 events; ET alone, 70 events) and DDFS did not reach the planned numbers of events. Eight-year DFS/DDFS rates were 86%/93% and 83%/92%, respectively. DFS was significantly better in CT+ET than ET alone in subgroups aged < 60 years (P = 0.016), T2 (P = 0.013), or Ki67 > 20% (P = 0.026). Progesterone receptor and histological grade were predictive markers for clinical responses to NET.
NET may be used as standard treatment for patients with ER+EBC. Although it is difficult to decide whether to administer adjuvant CT based solely on the effect of NET, the response to NET may help to inform this decision.
This study was registered at the UMIN Clinical Trials Registry under UMIN000001090 (registered 20 March 2008).
新辅助内分泌治疗(NET)是雌激素受体阳性(ER+)绝经后早期乳腺癌(EBC)的一种治疗选择。本 III 期试验评估了接受 NET 治疗后联合/不联合化疗(CT)的 EBC 患者的预后。
2008 年至 2013 年,纳入了 ER+/HER2-、T1c-2 和临床淋巴结阴性的 EBC 患者,并在第 24-28 周接受内分泌治疗(ET)。所有患者均接受 NET 治疗,除非 NET 期间疾病进展(PD)或术后淋巴结阳性数≥4。除 NET 期间疾病进展或术后淋巴结阳性数≥4 的患者外,其余患者均随机分为接受 ET 治疗 4.5-5 年联合/不联合 CT。主要终点是无病生存(DFS)。次要终点包括远处无病生存(DDFS)、总生存(OS)以及根据 NET 临床反应的 DFS/DDFS/OS。
904 例患者中,669 例患者被随机分为 CT+ET(n=333)或 ET 单药治疗(n=336)。中位随访时间为 7.8 年。DFS(CT+ET 组 47 例事件;ET 单药组 70 例事件)和 DDFS 未达到计划的事件数。8 年 DFS/DDFS 率分别为 86%/93%和 83%/92%。年龄<60 岁(P=0.016)、T2(P=0.013)或 Ki67>20%(P=0.026)的患者中,CT+ET 组的 DFS 明显优于 ET 单药组。孕激素受体和组织学分级是 NET 临床反应的预测标志物。
NET 可作为 ER+EBC 患者的标准治疗方法。尽管仅根据 NET 的效果决定是否给予辅助 CT 较为困难,但 NET 的反应可能有助于做出这一决定。
本研究在 UMIN 临床试验注册中心注册,注册号为 UMIN000001090(注册日期 2008 年 3 月 20 日)。