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Application and dosimetric requirements for 68Ga-labeled somatostatin analogues in targeted radionuclide therapy for gastroenteropancreatic neuroendocrine tumors

机译:68Ga标记的生长抑素类似物在胃肠道胰腺神经内分泌肿瘤靶向放射性核素治疗中的应用和剂量要求

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摘要

Neuroendocrine tumors (NETs) are associated with variable prognosis, with grade 1 and 2 NETs having a more favorable outcome than G3 ones (also called carcinoma). GEP-NET patients need highly individualized interdisciplinary evaluations and treatment. New treatment options have become available (i.e., sunitinib, mTOR inhibitors) with significant improvements in progression-free survival. Peptide receptor radionuclide therapy (PRRT) using 90Y or 177Lu-labeled somatostatin analogs has also shown promise in the treatment of advanced progressive NETs but randomized clinical trials comparing with other modalities are still lacking. SST-targeting represents the essence of theranostics. 68Ga-DOTA-SSTa can be used as companion imaging agents to assist in such a radionuclide therapy selection. 68Ga-DOTA-SSTa PET/CT might also provide critical information for prognosis, tumor response assessement to PRRT, and internal dosimetry. It is also expected that the development of novel receptor-targeting radiopharmaceuticals will contribute to the development of molecular-based personalized medicine approaches.
机译:神经内分泌肿瘤(NET)与预后的变化有关,其中1级和2级NET的预后要优于G3级(也称为癌)。 GEP-NET患者需要高度个性化的跨学科评估和治疗。已经有了新的治疗选择(即舒尼替尼,mTOR抑制剂),其无进展生存期得到了显着改善。使用 90 Y或 177 Lu标记的生长抑素类似物的肽受体放射性核素治疗(PRRT)在晚期进行性NETs的治疗中也显示出了希望,但与其他方式相比,已有随机临床试验仍然缺乏。以SST为目标代表了诊断学的本质。 68 Ga-DOTA-SSTa可用作伴随成像剂,以协助进行这种放射性核素治疗的选择。 68 Ga-DOTA-SSTa PET / CT还可能为预后,肿瘤对PRRT的反应评估以及内部剂量测定提供重要信息。还期望新型靶向受体的放射性药物的开发将有助于基于分子的个性化医学方法的开发。

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