Patient selection for CAR T or BiTE therapy in multiple myeloma: Which treatment for each patient?

David Kegyes1,2, Catalin Constantinescu1,2,3, Louise Vrancken4,5

  • 1Medfuture Research Center for Advanced Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.

Insights

Novel immunotherapies like CAR T cell therapy and bispecific T cell engagers show promise for treating multiple myeloma (MM). Early use of these T cell-based therapies may significantly improve outcomes for MM patients.

Area of Science:

  • Hematology
  • Immunology
  • Oncology

Background:

  • Multiple myeloma (MM) is a progressive plasma cell malignancy with increasing global incidence.
  • Despite advancements, MM remains incurable, necessitating novel therapeutic strategies.
  • Current treatments include stem cell transplantation for eligible patients.

Purpose of the Study:

  • To review and compare CAR T cell therapy (CAR) and bispecific T cell engagers (BiTE) for multiple myeloma.
  • To discuss the potential of T cell-based immunotherapies in MM treatment.
  • To explore the role of these immunotherapies as bridging therapies to transplant.

Main Methods:

  • Comprehensive review of existing clinical literature on CAR T cell therapy and BiTE in MM.
  • Comparative analysis of CAR T cell therapy and BiTE efficacy and safety.
  • Discussion of emerging therapeutic targets and future clinical trial designs.

Main Results:

  • CAR T cell therapy and BiTE target various MM surface antigens including BCMA, SLAMF7, GPRC5D, FCRH5, and CD38.
  • Evidence suggests early immunotherapy administration may enhance patient outcomes.
  • These immunotherapies are being investigated for their potential to improve MM treatment paradigms.

Conclusions:

  • CAR T cell therapy and BiTE represent promising T cell-based immunotherapies for multiple myeloma.
  • Early integration of these therapies could significantly impact MM patient outcomes.
  • Further research and clinical trials are warranted to optimize their use, potentially as bridging therapies.

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