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NAUTILUS试验中腋窝淋巴结评估的成像方案及标准

Imaging Protocol and Criteria for Evaluation of Axillary Lymph Nodes in the NAUTILUS Trial.

作者信息

Chang Jung Min, Shin Hee Jung, Choi Ji Soo, Shin Sung Ui, Choi Bo Hwa, Kim Min Jung, Yoon Jung Hyun, Chung Jin, Kim Tae Hee, Han Boo-Kyung, Kim Hak Hee, Moon Woo Kyung

机构信息

Department of Radiology, Seoul National University Hospital, Seoul, Korea.

Department of Radiology and Research Institute of Radiology, Asan Medical Center, Seoul, Korea.

出版信息

J Breast Cancer. 2021 Dec;24(6):554-560. doi: 10.4048/jbc.2021.24.e47. Epub 2021 Nov 24.

Abstract

Axillary ultrasonography (US) is the most commonly used imaging modality for nodal evaluation in patients with breast cancer. No Axillary Surgical Treatment in Clinically Lymph Node-Negative Patients after Ultrasonography (NAUTILUS) is a prospective, multicenter, randomized controlled trial investigating whether sentinel lymph node biopsy (SLNB) can be safely omitted in patients with clinically and sonographically node-negative T1-2 breast cancer treated with breast-conserving therapy. In this trial, a standardized imaging protocol and criteria were established for the evaluation of axillary lymph nodes. Women lacking palpable lymph nodes underwent axillary US to dismiss suspicious nodal involvement. Patients with a round hypoechoic node with effaced hilum or indistinct margins were excluded. Patients with T1 tumors and a single node with a cortical thickness ≥ 3 mm underwent US-guided biopsy. Finally, patients with negative axillary US findings were included. The NAUTILUS axillary US nodal assessment criteria facilitate the proper selection of candidates who can omit SLNB. Trial Registration: ClinicalTrials.gov Identifier: NCT04303715.

摘要

腋窝超声检查(US)是乳腺癌患者淋巴结评估中最常用的影像学检查方法。超声检查后临床淋巴结阴性患者不进行腋窝手术治疗(NAUTILUS)是一项前瞻性、多中心、随机对照试验,旨在研究对于接受保乳治疗的临床及超声检查淋巴结阴性的T1-2期乳腺癌患者,是否可以安全地省略前哨淋巴结活检(SLNB)。在该试验中,建立了标准化的影像学检查方案和标准用于腋窝淋巴结评估。未触及淋巴结的女性接受腋窝超声检查以排除可疑的淋巴结受累。圆形低回声结节且门部消失或边缘不清的患者被排除。T1期肿瘤且单个淋巴结皮质厚度≥3 mm的患者接受超声引导下活检。最后,纳入腋窝超声检查结果为阴性的患者。NAUTILUS腋窝超声淋巴结评估标准有助于正确选择可以省略SLNB的候选者。试验注册:ClinicalTrials.gov标识符:NCT04303715。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a76/8724375/d2677a9fedf0/jbc-24-554-g001.jpg

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