Maina Theodosia, Nock Berthold A, Kulkarni Harshad, Singh Aviral, Baum Richard P
Molecular Radiopharmacy, INRASTES, NCSR "Demokritos", Aghia Paraskevi, Athens 15310, Greece.
Molecular Radiopharmacy, INRASTES, NCSR "Demokritos", Aghia Paraskevi, Athens 15310, Greece.
PET Clin. 2017 Jul;12(3):297-309. doi: 10.1016/j.cpet.2017.02.007. Epub 2017 Apr 3.
Gastrin-releasing peptide receptors (GRPRs) represent attractive targets for cancer diagnosis and therapy owing to their overexpression in widespread human tumors. Bombesin (BBN) analogues coupled to suitable chelators for stable radiometal binding have been proposed for diagnostic imaging and radionuclide therapy (theranostics) of GRPR-positive tumors. Recently, interest has shifted from BBN-like receptor agonists to GRPR-radioantagonists, because radioantagonists do not induce adverse effects after injection to patients and display superior pharmacokinetic in vivo profiles. Thus, they seem more advantageous for clinical use compared to agonists. Newer developments highlighting the theranostic potential of GRPR-radioantagonists in cancer patient management are presented herein.
胃泌素释放肽受体(GRPRs)因其在多种人类肿瘤中过度表达,成为癌症诊断和治疗的有吸引力的靶点。已提出将与合适螯合剂偶联以实现稳定放射性金属结合的蛙皮素(BBN)类似物用于GRPR阳性肿瘤的诊断成像和放射性核素治疗(诊疗一体化)。最近,人们的兴趣已从类BBN受体激动剂转向GRPR放射性拮抗剂,因为放射性拮抗剂在注射给患者后不会引起不良反应,并且在体内显示出更优的药代动力学特征。因此,与激动剂相比,它们在临床应用中似乎更具优势。本文介绍了突出GRPR放射性拮抗剂在癌症患者管理中的诊疗一体化潜力的最新进展。