Monoclonal and Bispecific Anti-BCMA Antibodies in Multiple Myeloma

B-cell maturation antigen (BCMA), a member of the tumor necrosis factor receptor superfamily, is universally expressed by normal and neoplastic plasma cells and plays a critical role in the proliferation, survival and tumor progression in multiple myeloma (MM). B-cell activating factor (BAFF) and a...

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Main Authors: Benedetta Dalla Palma, Valentina Marchica, Maria Teresa Catarozzo, Nicola Giuliani, Fabrizio Accardi
Format: Article
Language:English
Published: MDPI AG 2020-09-01
Series:Journal of Clinical Medicine
Subjects:
Online Access:https://www.mdpi.com/2077-0383/9/9/3022
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author Benedetta Dalla Palma
Valentina Marchica
Maria Teresa Catarozzo
Nicola Giuliani
Fabrizio Accardi
author_facet Benedetta Dalla Palma
Valentina Marchica
Maria Teresa Catarozzo
Nicola Giuliani
Fabrizio Accardi
author_sort Benedetta Dalla Palma
collection DOAJ
description B-cell maturation antigen (BCMA), a member of the tumor necrosis factor receptor superfamily, is universally expressed by normal and neoplastic plasma cells and plays a critical role in the proliferation, survival and tumor progression in multiple myeloma (MM). B-cell activating factor (BAFF) and a proliferation-inducing ligand (APRIL) have been recognized as proliferation ligands for BCMA in the bone marrow microenvironment. Soluble BCMA levels in the serum correlates with disease phase and tumor burden and is a predictor of progression-free survival (PFS) and overall survival (OS). Recently, the introduction of new monoclonal antibodies against CD38 (Daratumumab and Isatuximab) and SLAM7 (Elotuzumab) has changed the therapeutic approach to MM, improving the response rate and the time to progression, both in newly diagnosed and refractory/relapsed patients. Among the surface antigens on MM cells, BCMA is a suitable target for the design of new antibody-based strategies. Experimental approaches targeting BCMA are currently being investigated and include antibody-drug conjugates (ADCs), bispecific antibodies (bsAbs) and genetically engineered T-cells with chimeric antigen receptors (CAR). In this review we summarize the more recent findings about BCMA biologic rationale as a therapeutic target and report the updated results of preclinical and clinical studies focused on ADCs and bsAbs targeting BCMA.
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spelling doaj.art-fc5f38bc1da0476387d0ca0c2b84254f2023-11-20T14:21:37ZengMDPI AGJournal of Clinical Medicine2077-03832020-09-0199302210.3390/jcm9093022Monoclonal and Bispecific Anti-BCMA Antibodies in Multiple MyelomaBenedetta Dalla Palma0Valentina Marchica1Maria Teresa Catarozzo2Nicola Giuliani3Fabrizio Accardi4Department of Medicine and Surgery, University of Parma, 43126 Parma, ItalyDepartment of Medicine and Surgery, University of Parma, 43126 Parma, ItalyDepartment of Medicine and Surgery, University of Parma, 43126 Parma, ItalyDepartment of Medicine and Surgery, University of Parma, 43126 Parma, ItalyDepartment of Medicine and Surgery, University of Parma, 43126 Parma, ItalyB-cell maturation antigen (BCMA), a member of the tumor necrosis factor receptor superfamily, is universally expressed by normal and neoplastic plasma cells and plays a critical role in the proliferation, survival and tumor progression in multiple myeloma (MM). B-cell activating factor (BAFF) and a proliferation-inducing ligand (APRIL) have been recognized as proliferation ligands for BCMA in the bone marrow microenvironment. Soluble BCMA levels in the serum correlates with disease phase and tumor burden and is a predictor of progression-free survival (PFS) and overall survival (OS). Recently, the introduction of new monoclonal antibodies against CD38 (Daratumumab and Isatuximab) and SLAM7 (Elotuzumab) has changed the therapeutic approach to MM, improving the response rate and the time to progression, both in newly diagnosed and refractory/relapsed patients. Among the surface antigens on MM cells, BCMA is a suitable target for the design of new antibody-based strategies. Experimental approaches targeting BCMA are currently being investigated and include antibody-drug conjugates (ADCs), bispecific antibodies (bsAbs) and genetically engineered T-cells with chimeric antigen receptors (CAR). In this review we summarize the more recent findings about BCMA biologic rationale as a therapeutic target and report the updated results of preclinical and clinical studies focused on ADCs and bsAbs targeting BCMA.https://www.mdpi.com/2077-0383/9/9/3022multiple myelomaB-cell maturation antigenmonoclonal antibody treatment
spellingShingle Benedetta Dalla Palma
Valentina Marchica
Maria Teresa Catarozzo
Nicola Giuliani
Fabrizio Accardi
Monoclonal and Bispecific Anti-BCMA Antibodies in Multiple Myeloma
Journal of Clinical Medicine
multiple myeloma
B-cell maturation antigen
monoclonal antibody treatment
title Monoclonal and Bispecific Anti-BCMA Antibodies in Multiple Myeloma
title_full Monoclonal and Bispecific Anti-BCMA Antibodies in Multiple Myeloma
title_fullStr Monoclonal and Bispecific Anti-BCMA Antibodies in Multiple Myeloma
title_full_unstemmed Monoclonal and Bispecific Anti-BCMA Antibodies in Multiple Myeloma
title_short Monoclonal and Bispecific Anti-BCMA Antibodies in Multiple Myeloma
title_sort monoclonal and bispecific anti bcma antibodies in multiple myeloma
topic multiple myeloma
B-cell maturation antigen
monoclonal antibody treatment
url https://www.mdpi.com/2077-0383/9/9/3022
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AT valentinamarchica monoclonalandbispecificantibcmaantibodiesinmultiplemyeloma
AT mariateresacatarozzo monoclonalandbispecificantibcmaantibodiesinmultiplemyeloma
AT nicolagiuliani monoclonalandbispecificantibcmaantibodiesinmultiplemyeloma
AT fabrizioaccardi monoclonalandbispecificantibcmaantibodiesinmultiplemyeloma