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首页> 外文期刊>Annals of surgical oncology >The Sentinel Lymph Node Biopsy Using Indocyanine Green Fluorescence Plus Radioisotope Method Compared With the Radioisotope-Only Method for Breast Cancer Patients After Neoadjuvant Chemotherapy: A Prospective, Randomized, Open-Label, Single-Center Phase 2 Trial
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The Sentinel Lymph Node Biopsy Using Indocyanine Green Fluorescence Plus Radioisotope Method Compared With the Radioisotope-Only Method for Breast Cancer Patients After Neoadjuvant Chemotherapy: A Prospective, Randomized, Open-Label, Single-Center Phase 2 Trial

机译:使用吲哚菁绿色荧光加号的Sentinel淋巴结活检与Neoadjuvant化疗后乳腺癌患者的仅限放射性同位素的方法相比:一项前瞻性,随机,开放标签,单中心2阶段试验

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BackgroundThis study aimed to compare the sentinel lymph node (SLN) identification rates for breast cancer patients after neoadjuvant chemotherapy (NAC) between the dual method (DM) of indocyanine green fluorescence (ICG-F) plus a radioisotope (RI) and RI alone.MethodsThis randomized study enrolled 130 patients who received NAC for breast cancer and 122 patients who received SLN biopsy (SLNB) using either DM (n=58) or RI only (n=64). The study compared the identification rate, number of SLNs, and detection time of SLNB.ResultsAmong the 122 patients, 113 (92.6%) were clinically node-positive before NAC. The SLN identification rate was 98.3% in the DM group and 93.8% in the RI group (p=0.14). The DM group and the RI group were similar in the average number of SLNs (2.21.13 vs. 1.9 +/- 1.33; p=0.26) and the time to detection of the first SLN (8.7 +/- 4.98 vs. 8.3 +/- 4.31min; p=0.30). In the DM group, transcutaneous lymphatic drainage was visualized by fluorescence imaging for 65.5% (38 of 58) of the patients. The SLN identification rate was 94.7% using ICG-F and 93% using RI (p=0.79). During and after the operation, no complications, including allergic reactions or skin necrosis, occurred.Conclusions p id=Par4 This study is the first randomized trial to use ICG-F for SLNB in breast cancer patients after NAC. The DM including ICG-F could be a feasible and safe method for SLNB in initially node-positive breast cancer patients with NAC.
机译:背景技术旨在将乳腺癌患者(NAc)与单独的放射性同位素(RI)和Ri之间的乳腺癌化疗(NAC)进行Neoadjuvant化疗(NAC)后的乳腺癌患者的Sentinel淋巴结(SLN)鉴定率。方法旨在研究患有130名接受NAC的130名乳腺癌和使用DM(n = 58)或RI接受SLN活检(SLNB)的122名患者(n = 64)。该研究比较了SLNB的识别率,SLN的数量和检测时间。培养122名患者,113例(92.6%)在NAC之前临床节点阳性。在DM组中,SLN识别率为98.3%,RI组中93.8%(P = 0.14)。 DM组和RI组在平均SLN(2.21.13与1.9 +/- 1.33; p = 0.26)以及检测第一个SLN的时间(8.7 +/- 4.98与8.3 + / - 4.31min; p = 0.30)。在DM组中,通过荧光成像可视化患者的经皮淋巴引流,可视化患者65.5%(38%)。使用ICG-F和93%使用RI(P = 0.79),SLN识别率为94.7%。在手术期间和之后,没有发生任何并发症,包括过敏反应或皮肤坏死。结论P id = PAR4本研究是在NAC后使用ICG-F在NAC后乳腺癌患者的ICG-F用于SLNB的第一个随机试验。包括ICG-F的DM可以是初始NAC初始阳性乳腺癌患者的SLNB可行和安全的方法。

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