Suppr超能文献

十年间使用间碘苄胍(MIBG)的经验以及新型放射性标记肽的潜力:个人概述与总结

Ten years of experience with MIBG applications and the potential of new radiolabeled peptides: a personal overview and concluding remarks.

作者信息

Shapiro B

机构信息

Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor 48109-0028, USA.

出版信息

Q J Nucl Med. 1995 Dec;39(4 Suppl 1):150-5.

PMID:9002776
Abstract

The international workshop on metaiodobenzylguanidine (MIBG) and radiolabeled somatostatin analogs held in Rome in June, 1994 addressed a wide range of topics which might be classified into five broad general themes: Theme 1. The role of MIBG for the location of neuroendocrine tumors. A) The range of tumors in which MIBG scintigraphy is effective (pheochromocytomas, neuroblastoma, chemodectoma and other APUDomas). B) The increasing popularity of 123I as a radiolabel for MIBG (potential advantages in planar and SPECT imaging). C) MIBG as the prototype of a family of radiopharmaceuticals exploiting the biogenic amine uptake and storage mechanisms. (Other radiohalides 124I, 125I, 87Br, 211At, 18F; other PET radiopharmaceuticals such as 11C-epinephrine, 11C-hydroxyephedrine). Theme 2. The role of MIBG as an in vivo scintigraphic probe of the sympathetic nervous system. A) Cardiac sympathetic innervation (in cardiomyopathy, myocardial infarction, and as a prognostic index for cardiac transplantation). B) Pulmonary MIBG uptake as index of pulmonary endothelial/sympathetic function (MIBG by both the intravenous and inhaled routes of administration). Theme 3. MIBG for the radiopharmaceutical therapy of neuroendocrine tumors. A) Treatment of neuroblastoma early in the natural history of the disease (MIBG therapy as initial management, MIBG therapy combined with other modalities--e.g., chemotherapy and bone marrow transplantation). Theme 4. The role of radiolabeled somatostatin analogs for the location of neuroendocrine and other tumors. A) The range of tumors in which somatostatin receptor radiopharmaceutical scintigraphy is effective (pituitary tumors, central nervous system tumors, carcinoids, islet cell tumors, medullary thyroid carcinoma, small cell lung cancer, APUDomas). B) The superiority of 111In over 123I as a radiolabel (the future of potential 99mTc and other labels). C) Somatostatin receptor scintigraphy in autoimmune and other disorders. D) Pentetreotide as the prototype of a wide range of radiolabeled peptides as radiopharmaceuticals for the in vivo depiction of the receptors for peptide hormones, lymphokines, paracrine and other information transmitting molecules (the general concepts include the use of long-acting, slowly degraded analogs and the development of generally applicable labeling techniques. Examples include 123I-ANF, labeled interleukins and other lymphokines). Theme 5. Comparisons of MIBG and pentetreotide scintigraphy for the location of neuroendocrine tumors. A) The range of neuroendocrine and other tumors (e.g., pheochromocytomas, neuroblastomas, carcinoids, islet cell tumors and other APUDomas).

摘要

1994年6月在罗马召开的关于间碘苄胍(MIBG)和放射性标记生长抑素类似物的国际研讨会探讨了广泛的主题,这些主题可大致分为五个宽泛的总体主题:主题1. MIBG在神经内分泌肿瘤定位中的作用。A)MIBG闪烁扫描有效的肿瘤范围(嗜铬细胞瘤、神经母细胞瘤、化学感受器瘤和其他APUD瘤)。B)123I作为MIBG放射性标记物的日益普及(在平面和SPECT成像中的潜在优势)。C)MIBG作为利用生物胺摄取和储存机制的一类放射性药物的原型。(其他放射性卤化物124I、125I、87Br、211At、18F;其他PET放射性药物,如11C - 肾上腺素、11C - 羟基麻黄碱)。主题2. MIBG作为交感神经系统体内闪烁扫描探针的作用。A)心脏交感神经支配(在心肌病、心肌梗死中,以及作为心脏移植的预后指标)。B)肺MIBG摄取作为肺内皮/交感神经功能指标(通过静脉和吸入给药途径的MIBG)。主题3. MIBG用于神经内分泌肿瘤的放射性药物治疗。A)在疾病自然史早期治疗神经母细胞瘤(MIBG治疗作为初始治疗,MIBG治疗与其他方式联合——例如化疗和骨髓移植)。主题4. 放射性标记生长抑素类似物在神经内分泌和其他肿瘤定位中的作用。A)生长抑素受体放射性药物闪烁扫描有效的肿瘤范围(垂体肿瘤、中枢神经系统肿瘤、类癌、胰岛细胞瘤、甲状腺髓样癌、小细胞肺癌、APUD瘤)。B)111In作为放射性标记物优于123I(潜在的99mTc和其他标记物的未来)。C)自身免疫和其他疾病中的生长抑素受体闪烁扫描。D)喷替肽作为一类广泛的放射性标记肽的原型,作为放射性药物用于体内描绘肽激素、淋巴因子、旁分泌和其他信息传递分子的受体(一般概念包括使用长效、缓慢降解的类似物以及开发普遍适用的标记技术。例子包括123I - 心钠素、标记的白细胞介素和其他淋巴因子)。主题5. MIBG和喷替肽闪烁扫描在神经内分泌肿瘤定位中的比较。A)神经内分泌和其他肿瘤的范围(例如嗜铬细胞瘤、神经母细胞瘤、类癌、胰岛细胞瘤和其他APUD瘤)。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验