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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.
Abstract:
Multiple myeloma (MM) is a plasma cell malignancy that affects an increasing number of patients worldwide. Despite all the efforts to understand its pathogenesis and develop new treatment modalities, MM remains an incurable disease. Novel immunotherapies, such as CAR T cell therapy (CAR) and bispecific T cell engagers (BiTE), are intensively targeting different surface antigens, such as BMCA, SLAMF7 (CS1), GPRC5D, FCRH5 or CD38. However, stem cell transplantation is still indispensable in transplant-eligible patients. Studies suggest that the early use of immunotherapy may improve outcomes significantly. In this review, we summarize the currently available clinical literature on CAR and BiTE in MM. Furthermore, we will compare these two T cell-based immunotherapies and discuss potential therapeutic approaches to promote development of new clinical trials, using T cell-based immunotherapies, even as bridging therapies to a transplant.
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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