Developmental trends in targeted radionuclide therapy of neuroendocrine tumors
محل انتشار: مجله پزشکی هسته ای ایران، دوره: 17، شماره: 2
سال انتشار: 1388
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 287
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شناسه ملی سند علمی:
JR_IRJNM-17-2_001
تاریخ نمایه سازی: 27 فروردین 1399
چکیده مقاله:
Neuroendocrine tumors (NETs) constitute a heterogeneous group of neoplasms including carcinoids, pancreatic neuroendocrine tumors, pituitary tumors, medullary thyroid carcinoma and phaeochromocytomas. The symptoms and the outcome of NETs differ considerably between patients depending on several factors. By labelling tracers with a radioisotope, the tracer acts as a carrier to deliver the radioactivity to tissues expressing somatostatin receptors (SSTRs) and may be used for diagnosis and treatment. Several factors influence the selection of an appropriate therapeutic radioisotope. A longer physical half-life and low dose rate may be more effective for relatively indolent malignancies such as NETs. Radiolabelled targeted therapy is a fairly recent and promising modality for the management of patients with inoperable or disseminated NETs when conventional therapies fail.
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نویسندگان
Mohamadreza Nouri Mahdavi
Department of Biomedical Radiation Sciences, Rudbeck Laboratory, Uppsala University, Uppsala, Sweden