CAR T-Cells in Multiple Myeloma: State of the Art and Future Directions

Despite recent therapeutic advances, the prognosis of multiple myeloma (MM) patients remains poor. Thus, new strategies to improve outcomes are imperative. Chimeric antigen receptor (CAR) T-cell therapy has changed the treatment landscape of B-cell malignancies, providing a potentially curative opti...

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Main Authors: Luis Gerardo Rodríguez-Lobato, Maya Ganzetti, Carlos Fernández de Larrea, Michael Hudecek, Hermann Einsele, Sophia Danhof
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-07-01
Series:Frontiers in Oncology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fonc.2020.01243/full
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spelling doaj-f873d6c5f8cc4da4902803586b2ce2ca2020-11-25T02:48:38ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2020-07-011010.3389/fonc.2020.01243541019CAR T-Cells in Multiple Myeloma: State of the Art and Future DirectionsLuis Gerardo Rodríguez-Lobato0Luis Gerardo Rodríguez-Lobato1Maya Ganzetti2Maya Ganzetti3Carlos Fernández de Larrea4Michael Hudecek5Hermann Einsele6Sophia Danhof7Division of Medicine II, University Hospital Würzburg, Würzburg, GermanyAmyloidosis and Multiple Myeloma Unit, Department of Hematology, Hospital Clínic of Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, SpainDivision of Medicine II, University Hospital Würzburg, Würzburg, GermanyUnit of Hematology and Bone Marrow Transplantation, IRCCS San Raffaele Scientific Institute, Milan, ItalyAmyloidosis and Multiple Myeloma Unit, Department of Hematology, Hospital Clínic of Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, SpainDivision of Medicine II, University Hospital Würzburg, Würzburg, GermanyDivision of Medicine II, University Hospital Würzburg, Würzburg, GermanyDivision of Medicine II, University Hospital Würzburg, Würzburg, GermanyDespite recent therapeutic advances, the prognosis of multiple myeloma (MM) patients remains poor. Thus, new strategies to improve outcomes are imperative. Chimeric antigen receptor (CAR) T-cell therapy has changed the treatment landscape of B-cell malignancies, providing a potentially curative option for patients who are refractory to standard treatment. Long-term remissions achieved in patients with acute lymphoblastic leukemia and Non-Hodgkin Lymphoma encouraged its further development in MM. B-cell maturation antigen (BCMA)-targeted CAR T-cells have established outstanding results in heavily pre-treated patients. However, several other antigens such as SLAMF7 and CD44v6 are currently under investigation with promising results. Idecabtagene vicleucel is expected to be approved soon for clinical use. Unfortunately, relapses after CAR T-cell infusion have been reported. Hence, understanding the underlying mechanisms of resistance is essential to promote prevention strategies and to enhance CAR T-cell efficacy. In this review we provide an update of the most recent clinical and pre-clinical data and we elucidate both, the potential and the challenges of CAR T-cell therapy in the future.https://www.frontiersin.org/article/10.3389/fonc.2020.01243/fullmultiple myelomaimmunotherapychimeric antigen receptorB-cell maturation antigenT-cellcytokine release syndrome
collection DOAJ
language English
format Article
sources DOAJ
author Luis Gerardo Rodríguez-Lobato
Luis Gerardo Rodríguez-Lobato
Maya Ganzetti
Maya Ganzetti
Carlos Fernández de Larrea
Michael Hudecek
Hermann Einsele
Sophia Danhof
spellingShingle Luis Gerardo Rodríguez-Lobato
Luis Gerardo Rodríguez-Lobato
Maya Ganzetti
Maya Ganzetti
Carlos Fernández de Larrea
Michael Hudecek
Hermann Einsele
Sophia Danhof
CAR T-Cells in Multiple Myeloma: State of the Art and Future Directions
Frontiers in Oncology
multiple myeloma
immunotherapy
chimeric antigen receptor
B-cell maturation antigen
T-cell
cytokine release syndrome
author_facet Luis Gerardo Rodríguez-Lobato
Luis Gerardo Rodríguez-Lobato
Maya Ganzetti
Maya Ganzetti
Carlos Fernández de Larrea
Michael Hudecek
Hermann Einsele
Sophia Danhof
author_sort Luis Gerardo Rodríguez-Lobato
title CAR T-Cells in Multiple Myeloma: State of the Art and Future Directions
title_short CAR T-Cells in Multiple Myeloma: State of the Art and Future Directions
title_full CAR T-Cells in Multiple Myeloma: State of the Art and Future Directions
title_fullStr CAR T-Cells in Multiple Myeloma: State of the Art and Future Directions
title_full_unstemmed CAR T-Cells in Multiple Myeloma: State of the Art and Future Directions
title_sort car t-cells in multiple myeloma: state of the art and future directions
publisher Frontiers Media S.A.
series Frontiers in Oncology
issn 2234-943X
publishDate 2020-07-01
description Despite recent therapeutic advances, the prognosis of multiple myeloma (MM) patients remains poor. Thus, new strategies to improve outcomes are imperative. Chimeric antigen receptor (CAR) T-cell therapy has changed the treatment landscape of B-cell malignancies, providing a potentially curative option for patients who are refractory to standard treatment. Long-term remissions achieved in patients with acute lymphoblastic leukemia and Non-Hodgkin Lymphoma encouraged its further development in MM. B-cell maturation antigen (BCMA)-targeted CAR T-cells have established outstanding results in heavily pre-treated patients. However, several other antigens such as SLAMF7 and CD44v6 are currently under investigation with promising results. Idecabtagene vicleucel is expected to be approved soon for clinical use. Unfortunately, relapses after CAR T-cell infusion have been reported. Hence, understanding the underlying mechanisms of resistance is essential to promote prevention strategies and to enhance CAR T-cell efficacy. In this review we provide an update of the most recent clinical and pre-clinical data and we elucidate both, the potential and the challenges of CAR T-cell therapy in the future.
topic multiple myeloma
immunotherapy
chimeric antigen receptor
B-cell maturation antigen
T-cell
cytokine release syndrome
url https://www.frontiersin.org/article/10.3389/fonc.2020.01243/full
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