Lee Eun-Gyeong, Lee Dong-Eun, Jung So-Youn, Han Jai Hong, Kim Seok-Ki, Chae Heejung, Sim Sung Hoon, Lee Keun Seok, Lee Seeyoun
Department of Surgery, Center for Breast Cancer, National Cancer Center, Goyang-si, Gyeonggi-do, Republic of Korea.
Biostatics Collaboration Team, Research Core Center, Research Institute of National Cancer Center, Goyang, Republic of Korea.
Ann Surg Oncol. 2025 Jun 30. doi: 10.1245/s10434-025-17740-9.
Neoadjuvant chemotherapy (NAC) leads to a nodal pathologic complete response (pCR) in approximately 70% of breast cancer patients, especially in human epidermal growth factor receptor 2 (HER2)-positive and triple-negative subtypes. However, sentinel lymph node (SLN)-mapping after NAC remains challenging due to lower identification and higher false-negative rates compared with early-stage breast cancer. This study aimed to evaluate the efficacy of a multimodal SLN-mapping approach after NAC.
This prospective, single-center, randomized controlled trial enrolled 270 patients with breast cancer receiving NAC between May 2021 and July 2024 and randomized them (1:1:1) to arm A (radioisotope [RI] + indocyanine green fluorescence [ICG-F]), arm B (RI + vital dye [indigo carmine]), and arm C (ICG-F + vital dye). The primary outcome of SLN-identification rate and the secondary outcome of SLN-operation time were analyzed.
Interim results showed SLN-identification rates of 95% in arm A, 92% in arm B, and 79% in arm C, with a significant difference between arms A and C (0.1597; p = 0.0055). The final analysis comparing only arms A and B showed SLN-identification rates of 92.6% (100/108) and 90.6% (96/106), respectively (p = 0.2967), with a significantly shorter mean time to first SLN detection in arm B than in arm A (7 vs. 8 min; p = 0.0046). The intra-arm detection rates differed significantly: arm A (RI, 96.0%; ICG-F, 92.0%; p = 0.232) versus arm B (RI, 97.9%; vital dye, 72.9%; p < 0.0001).
Multimodal SLN-mapping demonstrated high post-NAC identification rates without significant intra-arm differences in the SLN-identification rates, whereas SLN-detection rates differed by the method for each arm. For patients with breast cancer, RI + ICG-F SLN-mapping is an effective dual-method post-NAC approach.
新辅助化疗(NAC)可使约70%的乳腺癌患者实现腋窝淋巴结病理完全缓解(pCR),尤其是人表皮生长因子受体2(HER2)阳性和三阴性亚型患者。然而,与早期乳腺癌相比,NAC后的前哨淋巴结(SLN)定位仍然具有挑战性,原因在于识别率较低且假阴性率较高。本研究旨在评估NAC后多模式SLN定位方法的疗效。
本前瞻性、单中心、随机对照试验纳入了2021年5月至2024年7月期间接受NAC的270例乳腺癌患者,并将其按1:1:1随机分为A组(放射性同位素[RI]+吲哚菁绿荧光[ICG-F])、B组(RI+活性染料[靛胭脂])和C组(ICG-F+活性染料)。分析SLN识别率的主要结局和SLN手术时间的次要结局。
中期结果显示,A组的SLN识别率为95%,B组为92%,C组为79%,A组和C组之间存在显著差异(0.1597;p = 0.0055)。仅比较A组和B组的最终分析显示,SLN识别率分别为92.6%(100/108)和90.6%(96/106)(p = 0.2967),B组首次检测到SLN的平均时间显著短于A组(7分钟对8分钟;p = 0.0046)。组内检测率存在显著差异:A组(RI,96.0%;ICG-F,92.0%;p = 0.232)与B组(RI,97.9%;活性染料,72.9%;p < 0.0001)。
多模式SLN定位显示NAC后的识别率较高,且组内SLN识别率无显著差异,而各臂的SLN检测率因方法而异。对于乳腺癌患者,RI + ICG-F SLN定位是一种有效的NAC后双方法。