Novel immunotherapies in multiple myeloma.

Int J Hematol

Division of Immuno-Gene and Cell Therapy (Takara Bio), Jichi Medical University, Shimotsuke, Tochigi, Japan.

Published: June 2022

AI Article Synopsis

  • - The treatment landscape for multiple myeloma (MM) has changed significantly since the 1990s with the introduction of novel therapies, though some patients still experience poor outcomes.
  • - Recent advancements target the dysfunctional immune environment, focusing on therapies that reactivate the immune system to fight MM, especially in tough cases where traditional treatments have failed.
  • - This review highlights three innovative approaches currently being tested: checkpoint inhibitors to overcome immunosuppression, vaccines to boost anti-tumor immunity, and adoptive cell therapy to enhance immune responses, along with updates on ongoing clinical trials.

Article Abstract

For a substantial period, options for the treatment of multiple myeloma (MM) were limited; however, the advent of novel therapies into clinical practice in the 1990s resulted in dramatic changes in the prognosis of the disease. Subsequently, new proteasome inhibitors and immunomodulators with innovations in efficacy and toxicity were introduced; yet there remains a spectrum of patients with poor outcomes with current treatment strategies. One of the causes of disease progression in MM is the loss of the ability of the dysfunctional immune environment to control virulent cell clones. In recent years, therapies to overcome the immunosuppressive tumor microenvironment and activate the host immune system have shown promise in MM, especially in relapsed and refractory disease. Clinical use of this approach has been approved for several immunotherapies, and a number of studies are currently underway in clinical trials. This review outlines three of the newest and most promising approaches being investigated to enhance the immune system against MM: (1) overcoming immunosuppression with checkpoint inhibitors, (2) boosting immunity against tumors with vaccines, and (3) enhancing immune effectors with adoptive cell therapy. Information on the latest clinical trials in each class will be provided, and further developments will be discussed.

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Source
http://dx.doi.org/10.1007/s12185-022-03365-1DOI Listing

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