Department of Nuclear Medicine, School of Medicine, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.
Department of Nuclear Medicine, School of Medicine, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany
J Nucl Med. 2019 Sep;60(Suppl 2):13S-19S. doi: 10.2967/jnumed.118.220566.
Molecular alterations in malignant disease result in the expression or upregulations of various targets that can be used for imaging and treatment with radiopharmaceuticals. This theranostic principle has acquired greater importance in personalized medicine in recent years, particularly in oncology, where advanced tumors can be treated effectively with low side effects. Since the pioneering use of I in differentiated thyroid cancer in the 1940s, remarkable achievements in nuclear medicine endoradiotherapy have been demonstrated, mainly in the treatment of neuroendocrine neoplasms by using Lu-labeled somatostatin analogs or in the treatment of advanced prostate cancer using prostate-specific membrane antigen-directed radionuclide therapy. Besides that, this review focuses on promising novel radiopharmaceuticals and describes their preclinical and clinical status. Radiolabeled antibodies, such as I-omburtamab directed against the B7-H3 protein on the surface of neuroblastoma cells; HuMab-5B1, a Zr/Lu-labeled antibody for the treatment of CA19-9-expressing malignancies; and Lu-lilotomab, a CD37 antibody for the treatment of B-cell lymphomas, are being highlighted. The neurotensin receptor ligand In/Lu-3B-227 has demonstrated high potential in imaging and therapy for several malignancies (e.g., pancreatic adenocarcinomas). Targeting of the fibroblast activation protein is currently being explored for different tumor entities using PET imaging with the fibroblast activation protein inhibitor (FAPI) Ga-FAPI-04, and the first therapeutic applications of Y-FAPI-04 have been applied. After 2 decades of rapid development in theranostics, a variety of new targets are available for further clinical investigation.
恶性肿瘤中的分子改变导致各种靶标的表达或上调,这些靶标可用于放射性药物的成像和治疗。近年来,在个性化医疗中,这种治疗诊断学原理变得更加重要,特别是在肿瘤学中,先进的肿瘤可以通过低副作用的方式得到有效治疗。自 20 世纪 40 年代 I 在分化型甲状腺癌中的开创性应用以来,核医学内照射治疗已经取得了显著的成就,主要是通过使用 Lu 标记的生长抑素类似物治疗神经内分泌肿瘤,或通过使用前列腺特异性膜抗原导向放射性核素治疗治疗晚期前列腺癌。除此之外,本文还重点介绍了有前途的新型放射性药物,并描述了它们的临床前和临床现状。放射性标记的抗体,如针对神经母细胞瘤细胞表面 B7-H3 蛋白的 I-omburtamab;用于治疗表达 CA19-9 的恶性肿瘤的 Zr/Lu 标记抗体 HuMab-5B1;以及用于治疗 B 细胞淋巴瘤的 Lu-lilotomab,都是 CD37 抗体,都具有很大的治疗潜力。神经降压素受体配体 In/Lu-3B-227 在多种恶性肿瘤(如胰腺腺癌)的成像和治疗方面具有很高的潜力。目前正在使用成纤维细胞激活蛋白抑制剂(FAPI)Ga-FAPI-04 进行正电子发射断层扫描(PET)成像,探索针对不同肿瘤实体的成纤维细胞激活蛋白的靶向治疗,已经应用了 Y-FAPI-04 的首次治疗应用。在治疗诊断学快速发展的 20 年中,已经有多种新的靶点可供进一步的临床研究。