Clinical Cooperation Unit Molecular Hematology/Oncology, German Cancer Research Center (DKFZ) and Department of Internal Medicine V, University of Heidelberg, Heidelberg, Germany.
Department of Internal Medicine V, Heidelberg University Hospital, Heidelberg, Germany.
Mol Cancer Ther. 2021 Feb;20(2):367-378. doi: 10.1158/1535-7163.MCT-20-0287. Epub 2020 Dec 9.
Despite major treatment advances in recent years, patients with multiple myeloma inevitably relapse. The RNA polymerase II complex has been identified as a promising therapeutic target in both proliferating and dormant cancer cells. Alpha-amanitin, a toxin so far without clinical application due to high liver toxicity, specifically inhibits this complex. Here, we describe the development of HDP-101, an anti-B-cell maturation antigen (BCMA) antibody conjugated with an amanitin derivative. HDP-101 displayed high efficacy against both proliferating and resting myeloma cells , sparing BCMA-negative cells. In subcutaneous and disseminated murine xenograft models, HDP-101 induced tumor regression at low doses, including durable complete remissions after a single intravenous dose. In cynomolgus monkeys, HDP-101 was well tolerated with a promising therapeutic index. In conclusion, HDP-101 safely and selectively delivers amanitin to myeloma cells and provides a novel therapeutic approach to overcome drug resistance in this disease.
尽管近年来在治疗方面取得了重大进展,但多发性骨髓瘤患者仍不可避免地会复发。RNA 聚合酶 II 复合物已被确定为增殖和休眠癌细胞中有前途的治疗靶点。α-鹅膏蕈碱是一种由于肝脏毒性高而迄今尚未临床应用的毒素,它特异性地抑制该复合物。在这里,我们描述了 HDP-101 的开发,这是一种与鹅膏蕈碱衍生物偶联的抗 B 细胞成熟抗原 (BCMA) 抗体。HDP-101 对增殖和静止的骨髓瘤细胞均显示出高效性,对 BCMA 阴性细胞没有影响。在皮下和播散性鼠异种移植模型中,HDP-101 以低剂量诱导肿瘤消退,包括单次静脉注射后持久的完全缓解。在食蟹猴中,HDP-101 具有良好的耐受性和有前途的治疗指数。总之,HDP-101 可安全且选择性地将鹅膏蕈碱递送至骨髓瘤细胞,并为克服该疾病的耐药性提供了一种新的治疗方法。