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乳腺癌联合放射性和荧光引导前哨淋巴结活检的临床试验。

Clinical trial of combined radio- and fluorescence-guided sentinel lymph node biopsy in breast cancer.

机构信息

Department of Surgery, Leiden University Medical Centre, Leiden, The Netherlands.

出版信息

Br J Surg. 2013 Jul;100(8):1037-44. doi: 10.1002/bjs.9159. Epub 2013 May 21.

Abstract

BACKGROUND

Combining radioactive colloids and a near-infrared (NIR) fluorophore permits preoperative planning and intraoperative localization of deeply located sentinel lymph nodes (SLNs) with direct optical guidance by a single lymphatic tracer. The aim of this clinical trial was to evaluate and optimize a hybrid NIR fluorescence and radioactive tracer for SLN detection in patients with breast cancer.

METHODS

Patients with breast cancer undergoing SLN biopsy were enrolled. The day before surgery, a periareolar injection of indocyanine green (ICG)-99mTc-radiolabelled nanocolloid was administered and a lymphoscintigram acquired. Blue dye was injected immediately before surgery. Intraoperative SLN localization was performed using a γ probe and the Mini-FLARE™ NIR fluorescence imaging system. Patients were divided into two dose groups, with one group receiving twice the particle density of ICG and nanocolloid, but the same dose of radioactive 99mTc.

RESULTS

Thirty-two patients were enrolled in the trial. At least one SLN was identified before and during operation. All 48 axillary SLNs could be detected by γ tracing and NIR fluorescence imaging, but only 42 of them stained blue. NIR fluorescence imaging permitted detection of lymphatic vessels draining to the SLN up to 29 h after injection. Doubling the particle density did not yield a difference in fluorescence intensity (median 255 (range 98-542) versus 284 (90-921) arbitrary units; P = 0.590) or signal-to-background ratio (median 5·4 (range 3·0-15·4) versus 4·9 (3·5-16·3); P = 1·000) of the SLN.

CONCLUSION

The hybrid NIR fluorescence and radioactive tracer permitted accurate preoperative and intraoperative detection of the SLNs in patients with breast cancer.

REGISTRATION NUMBER

NTR3685 (Netherlands Trial Register; http://www.trialregister.nl).

摘要

背景

放射性胶体与近红外(NIR)荧光染料结合,可通过单个淋巴示踪剂进行直接光学引导,从而对深部前哨淋巴结(SLN)进行术前规划和术中定位。本临床试验旨在评估和优化一种新型的近红外荧光和放射性示踪剂,用于检测乳腺癌患者的 SLN。

方法

入组接受 SLN 活检的乳腺癌患者。手术前一天,在乳晕周围注射吲哚菁绿(ICG)-99mTc 放射性标记纳米胶体,并获取淋巴闪烁图。在手术前立即注射蓝色染料。使用 γ 探头和 Mini-FLARE™近红外荧光成像系统进行术中 SLN 定位。患者分为两组,一组接受两倍的 ICG 和纳米胶体的粒子密度,但放射性 99mTc 的剂量相同。

结果

本试验共入组 32 例患者。在术前和术中至少可识别出一个 SLN。γ 追踪和 NIR 荧光成像可检测到所有 48 个腋窝 SLN,但只有 42 个 SLN 染色为蓝色。NIR 荧光成像可在注射后 29 小时内检测到引流至 SLN 的淋巴管。将粒子密度增加一倍并未导致荧光强度(中位数 255(范围 98-542)与 284(90-921)任意单位;P=0.590)或 SLN 的信号-背景比(中位数 5·4(范围 3·0-15·4)与 4·9(3·5-16·3);P=1·000)有差异。

结论

该新型近红外荧光和放射性示踪剂可准确检测乳腺癌患者的 SLN,无论是术前还是术中。

注册号

NTR3685(荷兰试验注册处;http://www.trialregister.nl)。

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