多发性骨髓瘤
抗体
医学
癌症研究
药品
药理学
细胞生长
体外
免疫学
生物
生物化学
作者
Vianihuini Figueroa-Vazquez,Jonathan Ko,Christian Breunig,Anja Baumann,Nicola Giesen,Anikó Pálfí,Christoph Müller,Christian Lutz,Torsten Hechler,Michael Kulke,Carsten Müller‐Tidow,Alwin Krämer,Hartmut Goldschmidt,Andreas Pahl,Marc S. Raab
标识
DOI:10.1158/1535-7163.mct-20-0287
摘要
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 in vitro, 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.
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