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.

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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