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一种新的荧光靶向示踪剂对比乳腺癌前哨淋巴结活检中的双示踪剂。

A new fluorescenttargeting tracer contrasts dual tracers in sentinel lymph node biopsy of breast cancer.

机构信息

General Surgery, Kailuan General Hospital, Tangshan, Heibei, 063000, China.

Department of Breast Surgery, Yuncheng Central Hospital, Yuncheng, 044000, China.

出版信息

Future Oncol. 2024 May;20(14):951-958. doi: 10.2217/fon-2021-1152. Epub 2023 Nov 29.

Abstract

To explore the clinical application value of indocyanine green (ICG)-rituximab in sentinel lymph node biopsy. This study included 156 patients with primary breast cancer: 50 patients were enrolled in dose-climbing test, and 106 patients were enrolled in verification test. This was to compare the consistency of ICG-rituximab and combined method in the detected lymph nodes. According to the verification test, the imaging rate of ICG-rituximab was 97.3%. Compared with the combined method, the concordance rate of fluorescence method was 0.991 (28 + 78/107; p < 0.001). For ICG-rituximab as a fluorescent targeting tracer, the optimal imaging dose of ICG 93.75 μg/rituximab 375 μg can significantly reduce the imaging of secondary lymph nodes. Compared with the combined method, it has a higher concordance rate.

摘要

探讨吲哚菁绿(ICG)-利妥昔单抗在前哨淋巴结活检中的临床应用价值。本研究纳入了 156 例原发性乳腺癌患者:50 例患者纳入剂量爬坡试验,106 例患者纳入验证试验。旨在比较 ICG-利妥昔单抗与联合方法检测的淋巴结的一致性。根据验证试验,ICG-利妥昔单抗的成像率为 97.3%。与联合方法相比,荧光法的符合率为 0.991(28+78/107;p<0.001)。对于 ICG-利妥昔单抗作为荧光靶向示踪剂,ICG 的最佳成像剂量为 93.75μg/利妥昔单抗 375μg,可显著减少二级淋巴结的成像。与联合方法相比,具有更高的符合率。

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