Department of Surgery, BreastCare Center, Beth Israel Deaconess Medical Center/Harvard Medical School, Boston, MA, USA.
Ann Surg Oncol. 2021 Mar;28(3):1320-1325. doi: 10.1245/s10434-020-09382-w. Epub 2021 Jan 3.
Oncotype DX recurrence score (RS) is well-recognized for guiding decision making in adjuvant chemotherapy; however, the predictive capability of this genomic assay in determining axillary response to neoadjuvant chemotherapy (NCT) has not been established.
Using the National Cancer Data Base (NCDB), we identified patients diagnosed with T1-T2, clinically N1/N2, estrogen receptor-positive/human epidermal growth factor receptor 2-negative (ER +/HER2 -) invasive ductal carcinoma of the breast between 2010 and 2015. Patients with an Oncotype DX RS who received NCT were included. RS was defined as low (< 18), intermediate (18-30), or high (> 30). Unadjusted and adjusted analyses were performed to determine the association between axillary pathologic complete response (pCR) and RS.
This study included a total of 158 women. RS was low in 56 (35.4%) patients, intermediate in 62 (39.2%) patients, and high in 40 (25.3%) patients. The majority of patients presented with clinical N1 disease (89.2%). Axillary pCR was achieved in 23 (14.6%) patients. When stratifying patients with axillary pCR by RS, 11 (47.8%) patients had a high RS, 6 (26.1%) patients had an intermediate RS, and 6 (26.1%) patients had a low RS. Comparing cohorts by RS, 27.5% of patients with high RS tumors had an axillary pCR, compared with only 9.7% in the intermediate RS group, and 10.7% in the low RS group (p = 0.0268).
Our findings demonstrate that Oncotype DX RS is an independent predictor of axillary pCR in patients with ER +/HER2 - breast cancers receiving NCT. A greater proportion of patients with a high RS achieved axillary pCR. These results support Oncotype DX as a tool to improve clinical decision making in axillary management.
Oncotype DX 复发评分 (RS) 广泛用于指导辅助化疗决策;然而,该基因组检测在确定新辅助化疗 (NCT) 对腋窝的反应方面的预测能力尚未得到证实。
利用国家癌症数据库 (NCDB),我们确定了 2010 年至 2015 年间诊断为 T1-T2、临床 N1/N2、雌激素受体阳性/人表皮生长因子受体 2 阴性 (ER+/HER2-) 浸润性导管乳腺癌的患者。纳入接受 NCT 且有 Oncotype DX RS 的患者。RS 定义为低 (<18)、中 (18-30) 或高 (>30)。进行了未经调整和调整后的分析,以确定腋窝病理完全缓解 (pCR) 与 RS 之间的关系。
本研究共纳入 158 例患者。56 例 (35.4%) 患者 RS 低,62 例 (39.2%) 患者 RS 中,40 例 (25.3%) 患者 RS 高。大多数患者表现为临床 N1 疾病 (89.2%)。23 例 (14.6%) 患者达到腋窝 pCR。当根据 RS 对腋窝 pCR 患者进行分层时,11 例 (47.8%) 高 RS 患者,6 例 (26.1%) 中 RS 患者,6 例 (26.1%) 低 RS 患者。比较 RS 分组的患者,高 RS 肿瘤患者中 27.5% 有腋窝 pCR,而中 RS 组仅为 9.7%,低 RS 组为 10.7% (p=0.0268)。
我们的研究结果表明,在接受 NCT 的 ER+/HER2-乳腺癌患者中,Oncotype DX RS 是腋窝 pCR 的独立预测因素。高 RS 患者中更多的患者达到腋窝 pCR。这些结果支持 Oncotype DX 作为一种工具,可改善腋窝管理中的临床决策。