Jiao Rubin, Allen Kevin J H, Malo Mackenzie E, Yilmaz Orhan, Wilson John, Nelson Bryce J B, Wuest Frank, Dadachova Ekaterina
College of Pharmacy and Nutrition, University of Saskatchewan, Saskatoon, SK S7N 5E5, Canada.
Department of Oncology, Cross Cancer Institute, University of Alberta, Edmonton, AB T6G 1Z2, Canada.
Cancers (Basel). 2023 Jul 29;15(15):3856. doi: 10.3390/cancers15153856.
Metastatic melanoma is a deadly disease that claims thousands of lives each year despite the introduction of several immunotherapeutic agents into the clinic over the past decade, inspiring the development of novel therapeutics and the exploration of combination therapies. Our investigations target melanin pigment with melanin-specific radiolabeled antibodies as a strategy to treat metastatic melanoma. In this study, a theranostic approach was applied by first labeling a chimeric antibody targeting melanin, c8C3, with the SPECT radionuclide Pb for microSPECT/CT imaging of C57Bl6 mice bearing B16-F10 melanoma tumors. Imaging was followed by radioimmunotherapy (RIT), whereby the c8C3 antibody is radiolabeled with a Pb/Bi "in vivo generator", which emits cytotoxic alpha particles. Using microSPECT/CT, we collected sequential images of B16-F10 murine tumors to investigate antibody biodistribution. Treatment with the Pb/Bi-labeled c8C3 antibody demonstrated a dose-response in tumor growth rate in the 5-10 µCi dose range when compared to the untreated and radiolabeled control antibody and a significant prolongation in survival. No hematologic or systemic toxicity of the treatment was observed. However, administration of higher doses resulted in a biphasic tumor dose response, with the efficacy of treatment decreasing when the administered doses exceeded 10 µCi. These results underline the need for more pre-clinical investigation of targeting melanin with Pb-labeled antibodies before the clinical utility of such an approach can be assessed.
转移性黑色素瘤是一种致命疾病,尽管在过去十年中有几种免疫治疗药物进入临床,但每年仍有数千人死于该病,这激发了新型治疗方法的开发和联合疗法的探索。我们的研究以黑色素特异性放射性标记抗体靶向黑色素为策略,用于治疗转移性黑色素瘤。在本研究中,采用了一种诊疗一体化方法,首先用单光子发射计算机断层扫描(SPECT)放射性核素铅标记一种靶向黑色素的嵌合抗体c8C3,用于对携带B16-F10黑色素瘤肿瘤的C57Bl6小鼠进行显微SPECT/CT成像。成像后进行放射免疫治疗(RIT),即用一种发射细胞毒性α粒子的铅/铋“体内发生器”对c8C3抗体进行放射性标记。利用显微SPECT/CT,我们收集了B16-F10小鼠肿瘤的序列图像,以研究抗体的生物分布。与未治疗和放射性标记的对照抗体相比,用铅/铋标记的c8C3抗体治疗在5-10微居里剂量范围内显示出肿瘤生长速率的剂量反应,并显著延长了生存期。未观察到该治疗的血液学或全身毒性。然而,给予更高剂量会导致双相肿瘤剂量反应,当给药剂量超过10微居里时,治疗效果会降低。这些结果强调,在评估这种方法的临床实用性之前,需要对用铅标记抗体靶向黑色素进行更多的临床前研究。