作者
Marco Chinol, Lisa Bodei, Marta Cremonesi, Giovanni Paganelli
发表日期
2002/4/1
来源
Seminars in nuclear medicine
卷号
32
期号
2
页码范围
141-147
出版商
WB Saunders
简介
High concentrations of subtype 2 somatostatin tumor receptors (sst2) are expressed in numerous tumors, enabling primary and metastatic masses to be localized by scintigraphy after injecting 111In-labeled somatostatin analogue octreotide. In addition to neuroendocrine tumors, somatostatin receptors have been identified on cancers of the central nervous system, breast, lung, and lymphatic tissue, and the use of radionuclide-labeled somatostatin analogues appeared promising for therapy as well as for diagnosis of such malignancies. The somatostatin analogue [DOTA-DPhe1-Tyr3] octreotide (DOTATOC) possesses favorable characteristics for its potential therapeutic use in that it shows high affinity for sst2, moderately high affinity for sst5, and intermediate affinity for sst3, high hydrophilicity, stable and facile labeling with 111In and 90Y. We began to investigate the potential therapeutic applications of 90Y …
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