Brown Michael P, Bezak Eva, Allen Barry J
Translational Oncology Laboratory, Centre for Cancer Biology, SA Pathology & University of South Australia, Adelaide, SA, Australia.
School of Medicine, University of Adelaide, Adelaide, SA, Australia.
Melanoma Manag. 2015 Nov;2(4):353-366. doi: 10.2217/mmt.15.26. Epub 2015 Nov 24.
Standard treatments for metastatic melanoma have recently extended survival although many patients still succumb. Targeted alpha therapy (TAT) is a new therapeutic approach in which a cancer-targeting vector is labeled with an alpha-emitting radioisotope. Alpha-particles have the shortest range and highest energy transfer, and produce localized, high-density and lethal ionization damage to DNA. Thus, the targeted radiation can kill isolated cancer cells circulating in blood and lymphatic vessels, regress metastatic cancer cell clusters, and disrupt the vasculature of solid tumors. Preclinical and clinical studies of TAT for metastatic melanoma demonstrate its safety and anti-tumor activity. We recommend ways in which TAT can be used to treat small-volume disease sometimes in conjunction with cytoreductive anti-melanoma therapies.
转移性黑色素瘤的标准治疗方法最近延长了患者的生存期,尽管仍有许多患者最终死亡。靶向α治疗(TAT)是一种新的治疗方法,其中癌症靶向载体用发射α粒子的放射性同位素标记。α粒子射程最短、能量转移最高,可对DNA产生局部、高密度且致命的电离损伤。因此,靶向辐射可杀死血液和淋巴管中循环的孤立癌细胞,使转移性癌细胞团消退,并破坏实体瘤的脉管系统。TAT治疗转移性黑色素瘤的临床前和临床研究证明了其安全性和抗肿瘤活性。我们推荐了一些方法,通过这些方法,TAT有时可与减瘤性抗黑色素瘤疗法联合用于治疗小体积疾病。