New radiopharmaceuticals for receptor scintigraphy and radionuclide therapy.

I Virgolini, T Traub, M Leimer, C Novotny, T Pangerl, S Ofluoglu, E Halvadjieva, P Smith-Jones, J Flores, S R Li, P Angelberger, E Havlik, F Andreae, M Raderer, A Kurtaran, B Niederle, R Dudczak
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引用次数: 0

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.

用于受体显像和放射性核素治疗的新型放射性药物。
体外实验数据表明,神经内分泌来源的恶性细胞中存在大量的各种激素和多肽受体。其中,sst家族成员(hSSTR1-5)的结合位点经常被发现,它们的表达导致了特异性靶向这些受体的治疗和诊断尝试。使用放射性标记肽配体的受体闪烁成像已在临床实践中证明其有效性。此外,初步结果显示了受体靶向放疗的临床潜力。基于生长抑素(SST)受体(R)识别,维也纳大学开发的新型放射性药物111In/90Y-DOTA-lanreotide和111In/90Y-DOTA-DPhe1-Tyr3-octreotide (NOVARTIS)都为hsstr阳性肿瘤的诊断和治疗提供了有希望的数据。使用111in - dtpa - dphe1 -奥曲肽的SSTR显像对绝大多数神经内分泌肿瘤具有很高的阳性预测价值,在患者的诊断检查和随访中占有一席之地。自1997年以来,我们对166例患者使用了111In-DOTA-lanreotide显像,93%的患者结果为阳性。对42例神经内分泌肿瘤进行比较分析。与111in - dtpa - dphe1 -奥曲肽和111in - dota - dphe1 - tyr3 -奥曲肽相反,大约三分之一的患者在肿瘤摄取和肿瘤病变检测方面的扫描结果存在差异。90Y-DOTA-lanreotide和90Y-DOTA-DPhe1-Tyr3-octreotide的初步结果都指出了放射性核素受体靶向放疗的临床潜力。这种新疗法可以以较低的成本提供缓解和疾病控制。最终的肽治疗策略很可能比传统的放射治疗或长期化疗更便宜。总的来说,90Y-DOTA-lanreotide/90Y-DOTA-DPhe1-Tyr3-octre otide的受体介导放疗可能对传统策略难治性患者也有效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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