Friedman-Eldar Orli, Ozmen Tolga, El Haddi Salah James, Goel Neha, Tjendra Youley, Kesmodel Susan B, Moller Mecker G, Franceschi Dido, Layton Christina, Avisar Eli
Department of Surgical Oncology, Jackson Memorial Hospital, Miami, FL, USA.
Division of Surgical Oncology, DeWitt Daughtry Family Department of Surgery, University of Miami Miller School of Medicine, Miami, FL, USA.
Ann Surg Oncol. 2022 Mar 18. doi: 10.1245/s10434-022-11473-9.
One potential benefit of neoadjuvant therapy (NAT) in node-positive, estrogen receptor-positive (ER+), human epidermal growth factor receptor 2-negative (HER2-) patients is axillary downstaging to avoid axillary dissection.
The aim of this study was to evaluate axillary response to NAT with chemotherapy (NCT) or endocrine therapy (NET) and identify potential predictors of response.
A prospectively collected database was queried for node-positive, ER+, HER2- breast cancer patients treated with NAT and surgery from January 2011 to September 2020. Axillary response was categorized into pathologic complete response (pCR) versus no pCR, and was correlated to demographic and clinicopathologic parameters in a logistic regression model.
A cohort of 176 eligible patients was identified and 178 breast cancers were included in the study. The overall axillary pCR rate was 12.3% (22/178). NCT and NET achieved response rates of 13.9% (19/137) and 7.3% (3/41), respectively (p = 0.232). A significantly higher axillary pCR rate was identified in patients with clinical stage II at diagnosis (12/60, 20%) compared with stage III (10/118, 8.4%; p = 0.03). NET patients with ypN0 were younger and were treated for a longer period of time (>6 months). Completion axillary dissection was omitted in the majority (73.7%) of NCT patients achieving axillary pCR.
For patients with node-positive, ER+, HER2- breast cancer, a lower burden of disease at the time of diagnosis (stage II) is associated with a significantly higher axillary pCR, enabling those patients to be spared axillary dissection. Further studies are necessary to define the role of genomic profiling in predicting axillary response.
新辅助治疗(NAT)对于淋巴结阳性、雌激素受体阳性(ER+)、人表皮生长因子受体2阴性(HER2-)的患者而言,一个潜在益处是腋窝降期,从而避免腋窝淋巴结清扫术。
本研究旨在评估化疗新辅助治疗(NCT)或内分泌新辅助治疗(NET)对腋窝的反应,并确定反应的潜在预测因素。
查询一个前瞻性收集的数据库,纳入2011年1月至2020年9月期间接受NAT和手术治疗的淋巴结阳性、ER+、HER2-乳腺癌患者。腋窝反应分为病理完全缓解(pCR)和非pCR,并在逻辑回归模型中与人口统计学和临床病理参数相关联。
确定了一组176例符合条件的患者,共178例乳腺癌纳入研究。总体腋窝pCR率为12.3%(22/178)。NCT和NET的反应率分别为13.9%(19/137)和7.3%(3/41)(p = 0.232)。诊断时临床分期为II期的患者腋窝pCR率显著高于III期患者(12/60,20%对比10/118,8.4%;p = 0.03)。达到ypN0的NET患者更年轻,且治疗时间更长(>6个月)。大多数达到腋窝pCR的NCT患者(7