Department of Nuclear Medicine, College of Medicine, Korea University Guro Hospital, South Korea.
Eur J Cardiothorac Surg. 2010 Jun;37(6):1450-6. doi: 10.1016/j.ejcts.2010.01.012. Epub 2010 Mar 28.
In the previous report, to simplify the synthesis and labelling procedures and to improve the biological properties, we developed a novel mannose receptor-binding agent, technetium-99m human serum albumin (99mTc-MSA), for sentinel lymph node detection. This study is the first clinical trial designed to test the reliability and feasibility of sentinel node detection using this new radioactive agent in patients with stage I non-small cell lung cancer.
Forty-two patients (30 men, 12 women; mean age 63.3 + or - 8.9 years) that were candidates for lobectomy with mediastinal lymph node dissection for stage I non-small cell lung cancer were enrolled. A total dose of 1mCi of 99mTc-MSA in 0.2 ml was administered in one shot at the peritumoural region approximately 3h before surgery. The radioactivity in the lymph nodes was counted before (in vivo) and after (ex vivo) dissection with a hand-held gamma probe. A sentinel lymph node was defined as any node for which the radioactivity count was 5 times that of the resected lung tissue with the lowest count for the ex vivo counts. All harvested lymph nodes were cut into 2-mm slices and ultimately diagnosed by using formalin-fixed and paraffin-embedded sections with haematoxylin and eosin staining.
99mTc-MSA was taken up by the lymph nodes and its detection did not change until 21 h after the injection. The number of dissected lymph nodes per patient was 22.1 + or - 11.6 (range 4-57). Among 42 patients, the sentinel lymph nodes could be identified in 40 patients (95.2%). The number of sentinel lymph nodes identified was 2.3 + or - 1.1 stations (range 1-5) per patient. Ten out of 40 patients (25.0%) had metastases in 11 sentinel lymph nodes. Three of these 11 sentinel lymph nodes (27.3%) had skip metastases. No false-negative sentinel lymph nodes were detected in any of the 10 patients with N1 or N2 disease (0%). The relationship between in vivo and ex vivo results for mediastinal sentinel lymph nodes showed concurrence in 29 out of 40 patients (72.5%).
Intra-operative sentinel lymph node identification using 99mTc-MSA appears to be feasible and reliable in stage I non-small cell lung cancer.
在之前的报告中,为了简化合成和标记程序并提高生物特性,我们开发了一种新型的甘露糖受体结合剂,即锝 99m 人血清白蛋白(99mTc-MSA),用于前哨淋巴结检测。本研究是首次设计用于测试使用这种新型放射性药物在 I 期非小细胞肺癌患者中进行前哨淋巴结检测的可靠性和可行性的临床试验。
42 名患者(30 名男性,12 名女性;平均年龄 63.3±8.9 岁)入选,这些患者均适合行肺叶切除术和纵隔淋巴结清扫术治疗 I 期非小细胞肺癌。手术前约 3 小时,在肿瘤周围区域一次性给予 1mCi 的 99mTc-MSA,总量为 0.2ml。在手术前(体内)和手术后(体外)使用手持式伽马探针对淋巴结中的放射性进行计数。前哨淋巴结定义为任何淋巴结的放射性计数是切除肺组织中放射性最低的 5 倍。所有采集的淋巴结均切成 2mm 切片,最终通过使用福尔马林固定和石蜡包埋切片进行苏木精和伊红染色进行正式诊断。
99mTc-MSA 被淋巴结摄取,其检测结果在注射后 21 小时内没有变化。每位患者的淋巴结清扫数量为 22.1±11.6(范围 4-57)。在 42 名患者中,40 名患者(95.2%)可识别前哨淋巴结。每位患者识别的前哨淋巴结数量为 2.3±1.1 站(范围 1-5)。40 名患者中有 10 名(25.0%)在 11 个前哨淋巴结中发现转移。这 11 个前哨淋巴结中有 3 个(27.3%)发生跳跃转移。在 10 名 N1 或 N2 疾病(0%)患者中均未发现假阴性前哨淋巴结。40 名患者中,29 名(72.5%)患者的体内和体外纵隔前哨淋巴结结果一致。
在 I 期非小细胞肺癌中,术中使用 99mTc-MSA 识别前哨淋巴结似乎是可行且可靠的。