动态 F-FDG PET 淋巴显影术用于活体鉴定鼠黑色素瘤的淋巴结转移。
Dynamic F-FDG PET Lymphography for In Vivo Identification of Lymph Node Metastases in Murine Melanoma.
机构信息
Molecular Pharmacology Program, Memorial Sloan Kettering Cancer Center, New York, New York.
Department of Radiology, Memorial Sloan Kettering Cancer Center, New York, New York.
出版信息
J Nucl Med. 2018 Feb;59(2):210-215. doi: 10.2967/jnumed.117.196303. Epub 2017 Sep 14.
Positron lymphography using F-FDG followed by Cerenkov-guided resection of lymph nodes in healthy mice has previously been introduced by our group. Our aim in this study was to further assess the technique's potential beyond merely localizing sentinel lymph nodes. We now aimed to evaluate the potential of positron lymphography to characterize the nodes with respect to their tumor status in order to identify metastatic lymph nodes. We explored whether metastatic nodes could be distinguished from normal nodes via dynamic F-FDG lymphography, to then be resected under Cerenkov imaging guidance. A murine melanoma cell line highly metastatic to lymph nodes (B16F10) was implanted subcutaneously on the dorsal hind paw of C57 mice while the tumor-free contralateral leg served as an intraindividual control. A model of reactive lymph nodes after concanavalin A challenge served as an additional control to provide nonmalignant inflammatory lymphadenopathy. Dynamic PET/CT imaging was performed immediately after injection of F-FDG around the tumor or intracutaneously in the contralateral footpad. Furthermore, PET/CT and Cerenkov studies were performed repeatedly over time to follow the course of metastatic spread. In selected mice, popliteal lymph nodes underwent Cerenkov luminescence imaging. Hematoxylin and eosin staining was done to verify the presence of lymphatic melanoma infiltration. Positron lymphography using F-FDG was successfully performed on tumor-bearing and non-tumor-bearing mice, as well as on controls bearing sites of inflammation; the results clearly identified the sentinel lymph node basin and delineated the lymphatic drainage. Significantly prolonged retention of activity was evident in metastatic nodes as compared with controls without tumor. On the basis of these results, the contrast in detection and identification of metastatic lymph nodes was distinct and could be used for guided lymph node resection, such as by using Cerenkov luminescence imaging. However, retention after F-FDG lymphography was also seen in acute inflammatory lymphadenopathy. In a tumor model, significantly longer retention of the radiotracer during F-FDG lymphography was seen in metastatic than nonmetastatic lymph nodes, allowing for differentiation between the two and for selective resection of tumor-bearing nodes using Cerenkov imaging. Inflammation can be better differentiated in a subacute state.
我们小组之前已经介绍过使用 F-FDG 进行正电子淋巴成像,然后使用切伦科夫引导切除健康小鼠的淋巴结。我们在这项研究中的目的是进一步评估该技术的潜力,不仅限于定位前哨淋巴结。我们现在旨在评估正电子淋巴成像在确定转移性淋巴结方面对淋巴结肿瘤状态进行特征描述的潜力。我们探索了转移性淋巴结是否可以通过动态 F-FDG 淋巴成像来与正常淋巴结区分开来,然后在切伦科夫成像引导下切除。
一个高度转移性的鼠黑色素瘤细胞系(B16F10)被植入 C57 小鼠的背部后爪皮下,而肿瘤无的对侧腿部作为个体内对照。刀豆球蛋白 A 挑战后的反应性淋巴结模型作为额外的对照,提供非恶性炎症性淋巴结病。在肿瘤周围或对侧足底皮内注射 F-FDG 后,立即进行动态 PET/CT 成像。此外,随着转移性传播的进程,随时间重复进行 PET/CT 和切伦科夫研究。在选定的小鼠中,腘淋巴结接受切伦科夫发光成像。进行苏木精和伊红染色以验证是否存在淋巴黑色素瘤浸润。
成功地在荷瘤和非荷瘤小鼠以及患有炎症部位的对照小鼠上进行了 F-FDG 的正电子淋巴成像;结果清楚地识别了前哨淋巴结盆地并描绘了淋巴引流。与无肿瘤的对照相比,转移性淋巴结的放射性示踪剂保留时间明显延长。基于这些结果,转移性淋巴结的检测和识别的对比度明显,可以用于引导淋巴结切除,例如使用切伦科夫发光成像。然而,在急性炎症性淋巴结病中也观察到 F-FDG 淋巴成像后的保留。
在肿瘤模型中,在 F-FDG 淋巴成像期间,转移性淋巴结的放射性示踪剂保留时间明显长于非转移性淋巴结,允许对两者进行区分,并使用切伦科夫成像选择性切除肿瘤性淋巴结。在亚急性状态下可以更好地区分炎症。