Back to Search
Start Over
HDP-101, an Anti-BCMA Antibody–Drug Conjugate, Safely Delivers Amanitin to Induce Cell Death in Proliferating and Resting Multiple Myeloma Cells
- Source :
- Molecular Cancer Therapeutics. 20:367-378
- Publication Year :
- 2021
- Publisher :
- American Association for Cancer Research (AACR), 2021.
-
Abstract
- 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.
- Subjects :
- 0301 basic medicine
Cancer Research
Antibody-drug conjugate
Amanitins
Immunoconjugates
Mice, SCID
Mice
03 medical and health sciences
0302 clinical medicine
Therapeutic index
Antigen
medicine
Animals
Humans
Enzyme Inhibitors
Multiple myeloma
Cell Proliferation
Amanitin
Cell Death
biology
Cell growth
business.industry
medicine.disease
Disease Models, Animal
030104 developmental biology
Oncology
030220 oncology & carcinogenesis
Cancer cell
biology.protein
Cancer research
Female
Antibody
Multiple Myeloma
business
Subjects
Details
- ISSN :
- 15388514 and 15357163
- Volume :
- 20
- Database :
- OpenAIRE
- Journal :
- Molecular Cancer Therapeutics
- Accession number :
- edsair.doi.dedup.....fc4bada6ec5e1d93000278d5ab727acf