4.6 Review

Keeping Myeloma in Check: The Past, Present and Future of Immunotherapy in Multiple Myeloma

期刊

CANCERS
卷 13, 期 19, 页码 -

出版社

MDPI
DOI: 10.3390/cancers13194787

关键词

multiple myeloma; immunotherapy; IMiD; antibody; ADC; bi-specific antibody; CAR-T; vaccine

类别

资金

  1. Riney Family Foundation
  2. Leukemia and Lymphoma Society
  3. NSF
  4. NIH

向作者/读者索取更多资源

Multiple myeloma is an incurable disease characterized by malignant plasma cells, making it a prime target for modern immune therapy. Immune therapy for multiple myeloma can be categorized into IMiDs, targeted antibodies, adoptive cell transfer therapies, and vaccines, all showing advancements in improving antitumor activity and specificity.
Multiple myeloma is an incurable disease of malignant plasma cells and an ideal target for modern immune therapy. The unique plasma cell biology maintained in multiple myeloma, coupled with its hematological nature and unique bone marrow microenvironment, provide an opportunity to design specifically targeted immunotherapies that selectively kill transformed cells with limited on-target off-tumor effects. Broadly defined, immune therapy is the utilization of the immune system and immune agents to treat a disease. In the context of multiple myeloma, immune therapy can be subdivided into four main categories: immune modulatory imide drugs, targeted antibodies, adoptive cell transfer therapies, and vaccines. In recent years, advances in all four of these categories have led to improved therapies with enhanced antitumor activity and specificity. In IMiDs, modified chemical structures have been developed that improve drug potency while reducing dose limiting side effects. Targeted antibody therapies have resulted from the development of new selectively expressed targets as well as the development of antibody drug conjugates and bispecific antibodies. Adoptive cell therapies, particularly CAR-T therapies, have been enhanced through improvements in the manufacturing process, as well as through the development of CAR constructs that enhance CAR-T activation and provide protection from a suppressive immune microenvironment. This review will first cover in-class breakthrough therapies for each of these categories, as well as therapies currently utilized in the clinic. Additionally, this review will explore up and coming therapeutics in the preclinical and clinical trial stage.

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