Outcomes of targeted axillary radiation therapy with omission of axillary dissection in early breast cancer patients with one or two positive sentinel lymph nodes and extracapsular extension

对于早期乳腺癌患者,若仅有1或2个前哨淋巴结阳性且存在包膜外侵犯,则采用靶向腋窝放射治疗而不行腋窝淋巴结清扫术的疗效如何?

阅读:1

Abstract

PURPOSE: Axillary dissection has been shown to be equivalent to axillary radiotherapy in the AMAROS trial; however, extracapsular invasion of sentinel lymph nodes was not considered among the evaluated variables. The clinical significance of extracapsular extension (ECE) in one or two positive sentinel lymph nodes remains under investigation. This study aims to evaluate the impact of targeted axillary radiation therapy while omitting completion axillary lymph node dissection (ALND) in the presence of extracapsular extension. METHODS: A retrospective study was conducted between 2016 and 2023 involving cT1-2N0 breast cancer patients who did not receive neoadjuvant chemotherapy and underwent either breast-conserving surgery or mastectomy, with extracapsular extension present in one or two positive sentinel lymph nodes. RESULTS: Our study included 213 patients treated between 2016 and 2023, with a median follow-up of 48.07 months (range: 9.07-103.10 months). ECE was ≤ 2 mm in 201 patients (94.4%) and > 2 mm in 12 patients (5.6%). A total of 112 patients (52.6%) underwent completion ALND. Systemic recurrence occurred in 24 patients (11.3%), while local recurrence occurred in one patient (0.5%). The 5-year disease-free survival (DFS) rates were 86% in the completion axillary clearance (AC) group and 89% in the non-AC group. The estimated DFS rates for the entire study at 1, 3, and 5 years were 97%, 89%, and 86%, respectively. CONCLUSIONS: Within this single-institution study of early breast cancer patients with predominantly luminal A subtype and mostly limited ECE (≤ 2 mm) treated with targeted axillary radiation, omission of ALND did not result in inferior DFS compared to completion ALND. However, these findings are preliminary, hypothesis-generating, and limited by the retrospective design, short follow-up, and specific patient population studied. Prospective studies are needed to confirm these observations. TRIAL REGISTRATION: Retrospectively registered after the approval of Baheya Ethical Committee, IRB no. 202,304,030,017.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。