Gherghe M, Bordea C, Blidaru A
Department of Nuclear Medicine, "Prof. Dr. Al. Trestioreanu" Institute of Oncology, Bucharest, Romania.
"Carol Davila" University of Medicine and Pharmacy, Bucharest, Romania; Department of Oncologic Surgery II, "Prof. Dr. Al. Trestioreanu" Institute of Oncology, Bucharest, Romania.
J Med Life. 2015 Apr-Jun;8(2):176-80.
The identification and biopsy of the sentinel lymph node has become a standard method of treatment for stage I and II breast cancer in the last decades, taking into account the fact that the management of the axilla in patients with breast cancer has evolved from the routine lymphadenectomy to a selective attitude, based on the histopathological evaluation of the sentinel lymph node, as well as on the tumor and on the patients' characteristics. Since the introduction of the method into clinical practice, in 1994, different methods of identification have been used (radioisotope injection, vital blue dye, or, more recently, lipophilic contrast agent for ultrasound visualization or paramagnetic nanoparticles (NPs) or the method of indocyanine green fluorescence), each presenting certain limits, but the radioisotopic method proving the most accurate. Moreover, during the development of the method, beside the standard indications specific for T1 or T2 breast tumor, without clinical or imagistic axillary adenopathies, their extension to a series of other particular situations such as the following, has been tried: ductal carcinoma in situ, multicentre tumors, after excisional biopsy or tumors preoperatively treated by neoadjuvant chemotherapy. The aim of the paper is to present the progress made regarding the current stage in the use of sentinel lymph node technique in breast cancer, while mentioning the established indications, as well as the ones that are still debating and need further studies. Likewise, the cases in which the axillary lymph node dissection remains the major indication for treatment of the axilla, in patients with early stage breast cancer, will be discussed.
在过去几十年中,前哨淋巴结的识别与活检已成为I期和II期乳腺癌的标准治疗方法,这是考虑到乳腺癌患者腋窝的处理已从常规淋巴结清扫演变为基于前哨淋巴结的组织病理学评估、肿瘤情况及患者特征的选择性处理方式。自1994年该方法引入临床实践以来,已采用了不同的识别方法(放射性同位素注射、活性蓝色染料,或最近用于超声可视化的亲脂性造影剂、顺磁性纳米颗粒或吲哚菁绿荧光法),每种方法都有一定局限性,但放射性同位素方法最为准确。此外,在该方法的发展过程中,除了适用于T1或T2期乳腺肿瘤且无临床或影像学腋窝淋巴结肿大的标准适应证外,还尝试将其扩展到一系列其他特殊情况,如下:导管原位癌、多中心肿瘤、切除活检后或新辅助化疗术前治疗的肿瘤。本文的目的是介绍乳腺癌前哨淋巴结技术当前应用阶段所取得的进展,同时提及既定的适应证以及仍在争论且需要进一步研究的适应证。同样,还将讨论早期乳腺癌患者中腋窝淋巴结清扫仍是腋窝治疗主要适应证的情况。