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Daratumumab: a first-in-class CD38 monoclonal antibody for the treatment of multiple myeloma
Larysa Sanchez1, Yucai Wang1, David S Siegel2
1Department of Medicine, Rutgers New Jersey Medical School, Newark, NJ, USA.
Abstract:
Daratumumab is a human monoclonal antibody that targets CD38, a cell surface protein that is overexpressed on multiple myeloma (MM) cells. Preclinical studies have shown that daratumumab induces MM cell death through several mechanisms, including complement-dependent cytotoxicity (CDC), antibody-dependent cell-mediated cytotoxicity (ADCC), antibody-dependent cellular phagocytosis (ADCP), and apoptosis. Given the encouraging efficacy and acceptable safety profile of daratumumab demonstrated in clinical trials, daratumumab has emerged as a novel treatment option for myeloma and became the first monoclonal antibody approved by the FDA for the treatment of MM.
Insights
Daratumumab, a CD38-targeting monoclonal antibody, effectively treats multiple myeloma (MM) by inducing cancer cell death. Its FDA approval marks a significant advancement in MM therapy.
Area of Science:
- Oncology
- Immunology
- Pharmacology
Background:
- Multiple myeloma (MM) is a cancer of plasma cells.
- CD38 is a protein highly expressed on MM cells.
Purpose of the Study:
- To evaluate daratumumab as a novel treatment for multiple myeloma.
- To highlight the mechanisms of action and clinical efficacy of daratumumab.
Main Methods:
- Daratumumab, a human monoclonal antibody, targets CD38.
- Preclinical studies investigated mechanisms like complement-dependent cytotoxicity (CDC), antibody-dependent cell-mediated cytotoxicity (ADCC), antibody-dependent cellular phagocytosis (ADCP), and apoptosis.
Main Results:
- Daratumumab demonstrated efficacy in clinical trials for multiple myeloma.
- The antibody induces MM cell death via multiple immune-mediated and direct cytotoxic pathways.
Conclusions:
- Daratumumab is an effective and safe treatment option for multiple myeloma.
- Daratumumab is the first monoclonal antibody approved by the FDA for MM treatment.
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