Antibody-drug conjugate therapies in multiple myeloma-what's next on the horizon?
Monique Hartley-Brown1, Paul Richardson1
1Department of Medicine, Division of Medical Oncology, Harvard Medical School, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
Abstract:
Targeted immunotherapy has arisen over the past decade to the forefront of cancer care. Notably, targeted therapies such as antibody-drug conjugates (ADCs) are becoming more recognized for a novel approach in cancer treatment. The mechanism of action of ADCs incorporates a monoclonal antibody portion directed against the tumor cell antigen and attached to the tumoricidal portion via chemical linkage. The binding of the monoclonal antibody portion allows for tumor cell internalization of the ADC and precise release of the toxic payload within the cancer cell. Multiple myeloma (MM) is an incurable cancer for which belantamab mafodotin was the first-in-class ADC to achieve United States Food and Drug Administration (FDA) approval for treatment of this disease. Clinical trials are currently evaluating other ADCs in the treatment of MM. In this review, a look at the current ADCs being tested in MM clinical trials with a focus on those that are more promising and a potential next-in-line for FDA approval for treatment of MM is discussed.
Insights
Antibody-drug conjugates (ADCs) offer a novel approach to treating multiple myeloma (MM). This review examines promising ADCs in clinical trials, highlighting potential future FDA-approved therapies for this incurable cancer.
Area of Science:
- Oncology
- Immunotherapy
- Pharmacology
Background:
- Targeted immunotherapy, particularly antibody-drug conjugates (ADCs), has become a significant advancement in cancer care.
- ADCs utilize a monoclonal antibody to target tumor cells, delivering a cytotoxic payload directly to cancer cells for precise cancer treatment.
- Multiple myeloma (MM) is a challenging hematologic malignancy with limited curative options.
Purpose of the Study:
- To review current antibody-drug conjugates (ADCs) undergoing clinical trials for multiple myeloma (MM).
- To identify promising ADCs that may represent the next wave of FDA-approved treatments for MM.
- To provide an overview of the evolving landscape of ADC-based therapies in MM treatment.
Main Methods:
- Literature review of ongoing clinical trials evaluating ADCs in multiple myeloma.
- Analysis of the mechanisms of action and clinical data for selected ADCs.
- Focus on ADCs demonstrating significant promise for future regulatory approval.
Main Results:
- Belantamab mafodotin is the first-in-class ADC approved by the FDA for MM treatment.
- Several other ADCs are in various phases of clinical trials for MM, showing potential efficacy.
- The review highlights specific ADCs with promising profiles for subsequent FDA evaluation.
Conclusions:
- ADCs represent a rapidly advancing therapeutic strategy for multiple myeloma.
- Ongoing clinical trials are crucial for developing next-generation ADCs for MM.
- The future of MM treatment is increasingly influenced by targeted ADC therapies.
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