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用于受体闪烁显像和放射性核素治疗的新型放射性药物。

New radiopharmaceuticals for receptor scintigraphy and radionuclide therapy.

作者信息

Virgolini I, Traub T, Leimer M, Novotny C, Pangerl T, Ofluoglu S, Halvadjieva E, Smith-Jones P, Flores J, Li S R, Angelberger P, Havlik E, Andreae F, Raderer M, Kurtaran A, Niederle B, Dudczak R

机构信息

Department of Nuclear Medicine, University of Vienna, Austria.

出版信息

Q J Nucl Med. 2000 Mar;44(1):50-8.

Abstract

In vitro data have demonstrated a high amount of receptors for various hormones and peptides on malignant cells of neuroendocrine origin. Among these, binding sites for members of the SST-family (hSSTR1-5) are frequently found, and their expression has led to therapeutic and diagnostic attempts to specifically target these receptors. Receptor scintigraphy using radiolabeled peptide ligands has proven its effectiveness in clinical practice. In addition, initial results have indicated a clinical potential for receptor-targeted radiotherapy. Based on somatostatin (SST) receptor (R) recognition, the novel radiopharmaceuticals 111In/90Y-DOTA-lanreotide developed at the University of Vienna as well as 111In/90Y-DOTA-DPhe1-Tyr3-octreotide (NOVARTIS) both have provided promising data for diagnosis and treatment of hSSTR-positive tumors. SSTR scintigraphy using 111In-DTPA-DPhe1-octreotide has a high positive predictive value for the vast majority of neuroendocrine tumors and has gained its place in the diagnostic work-up as well as follow-up of patients. We have used 111In-DOTA-lanreotide scintigraphy in 166 patients since 1997 and have seen positive results in 93% of patients. In 42 patients with neuroendocrine tumors comparative data were obtained. As opposed to 111In-DTPA-DPhe1-octreotide and 111In-DOTA-DPhe1-Tyr3-octreotide, discrepancies in the scintigraphic results were seen in about one third of patients concerning both the tumor uptake as well as tumor lesion detection. Initial results both with 90Y-DOTA-lanreotide as well as 90Y-DOTA-DPhe1-Tyr3-octreotide has pointed out the clinical potential of radionuclide receptor-targeted radiotherapy. This new therapy could offer palliation and disease control at a reduced cost. The final peptide therapy strategy is most probably cheaper than conventional radiotherapies or prolonged chemotherapies. Overall, receptor-mediated radiotherapy with 90Y-DOTA-lanreotide/90Y-DOTA-DPhe1-Tyr3-octre otide might also be effective in patients refractory to conventional strategies.

摘要

体外数据表明,神经内分泌起源的恶性细胞上存在大量针对各种激素和肽的受体。其中,经常发现SST家族成员(hSSTR1 - 5)的结合位点,其表达促使人们尝试针对这些受体进行治疗和诊断。使用放射性标记肽配体的受体闪烁显像已在临床实践中证明了其有效性。此外,初步结果表明受体靶向放疗具有临床应用潜力。基于生长抑素(SST)受体(R)识别,维也纳大学研发的新型放射性药物111In/90Y - DOTA - 兰瑞肽以及111In/90Y - DOTA - D - Phe1 - Tyr3 - 奥曲肽(诺华公司)在hSSTR阳性肿瘤的诊断和治疗方面均提供了有前景的数据。使用111In - DTPA - D - Phe1 - 奥曲肽的SSTR闪烁显像对绝大多数神经内分泌肿瘤具有较高的阳性预测价值,并在患者的诊断检查和随访中占据了一席之地。自1997年以来,我们对166例患者使用了111In - DOTA - 兰瑞肽闪烁显像,93%的患者取得了阳性结果。对42例神经内分泌肿瘤患者获取了对比数据。与111In - DTPA - D - Phe1 - 奥曲肽和111In - DOTA - D - Phe1 - Tyr3 - 奥曲肽不同,在大约三分之一的患者中,肿瘤摄取以及肿瘤病灶检测方面的闪烁显像结果存在差异。90Y - DOTA - 兰瑞肽以及90Y - DOTA - D - Phe1 - Tyr3 - 奥曲肽的初步结果均指出了放射性核素受体靶向放疗的临床应用潜力。这种新疗法可以以较低成本提供姑息治疗和疾病控制。最终的肽治疗策略可能比传统放疗或延长化疗更便宜。总体而言,90Y - DOTA - 兰瑞肽/90Y - DOTA - D - Phe1 - Tyr3 - 奥曲肽的受体介导放疗对传统治疗策略难治的患者可能也有效。

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