Virgolini I, Patri P, Novotny C, Traub T, Leimer M, Füger B, Li S R, Angelberger P, Raderer M, Wogritsch S, Kurtaran A, Kletter K, Dudczak R
Department of Nuclear Medicine, University of Vienna, Austria.
Ann Oncol. 2001;12 Suppl 2:S41-5. doi: 10.1093/annonc/12.suppl_2.s41.
Based on the high number of somatostatin (SST) receptors expressed by neuroendocrine tumors, long-acting SST analogs have been successfully used for tumor detection. New developments point to the potential use of these types of radioligands for tumor-specific radionuclide therapy.
We have comparatively investigated the diagnostic capacity of the SST analog. 111In-DOTA-lanreotide (LAN), as opposed to 111ln-DOTA-DPhe1-Tyr3-octreotide (TOCT) in tumor patients. This article gives an overview of recent scintigraphic results compared to CT/MRI, 18F-FDG-PET, endoscopy and/or surgery in a threshold of 218 tumor patients.
As opposed to radiology, previously unknown tumor lesions were demonstrable by either SST radioligand in about one third of patients. In carcinoid patients, the SST scan sensitivity was 64% for LAN (18 of 28) and 87% (34 of 39) for TOCT, whereas the sensitivity was 100% in patients with (radioiodine-negative) thyroid cancer (17 of 17) for LAN and 95% for TOCT (20 of 21). Discordant scintigraphic results between LAN and TOCT (higher tumor uptake and/or visualisation of different lesions in the same patient) were also seen in patients with lymphoma, lung cancer and intestinal adenocarcinoma. In a direct comparison of both SST tracers in 38 tumor patients, LAN gave positive results in 35 of 38, TOCT in 36 of 38 and 18F-FDG-PET in 14 of 22 of the same patients. SST scan results obtained by both tracers were equivocal in 23 of 38 patients, but were better in 10 patients withTOCTand in 5 patients with LAN.
We conclude that both SST radioligands are suitable tracers for tumor imaging, but may give significantly different uptake results for different tumor types. Since the uptake is most important for tumor therapy, using either longacting SSTanalogs, and/or 90Y-labeled analogs, careful evaluation should be made prior to therapy.
基于神经内分泌肿瘤表达大量生长抑素(SST)受体,长效SST类似物已成功用于肿瘤检测。新进展表明这些类型的放射性配体在肿瘤特异性放射性核素治疗方面具有潜在用途。
我们比较研究了SST类似物111In-DOTA-兰瑞肽(LAN)与111In-DOTA-DPhe1-Tyr3-奥曲肽(TOCT)在肿瘤患者中的诊断能力。本文概述了218例肿瘤患者中与CT/MRI、18F-FDG-PET、内镜检查和/或手术相比的近期闪烁扫描结果。
与放射学检查不同,两种SST放射性配体在约三分之一的患者中均可显示先前未知的肿瘤病变。在类癌患者中,LAN的SST扫描敏感性为64%(28例中的18例),TOCT为87%(39例中的34例),而在(放射性碘阴性)甲状腺癌患者中,LAN的敏感性为100%(17例中的17例),TOCT为95%(21例中的20例)。在淋巴瘤、肺癌和肠腺癌患者中也观察到LAN和TOCT之间闪烁扫描结果不一致(同一患者中肿瘤摄取更高和/或不同病变的显影)。在38例肿瘤患者中对两种SST示踪剂进行直接比较,LAN在38例中的35例给出阳性结果,TOCT在38例中的36例,18F-FDG-PET在同一患者的22例中的14例。两种示踪剂获得的SST扫描结果在38例患者中的23例中不明确,但在10例使用TOCT的患者和5例使用LAN的患者中结果更好。
我们得出结论,两种SST放射性配体都是适合肿瘤成像的示踪剂,但对于不同肿瘤类型可能给出显著不同的摄取结果。由于摄取对肿瘤治疗最为重要,在使用长效SST类似物和/或90Y标记的类似物进行治疗之前,应进行仔细评估。