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      Daratumumab with lenalidomide and dexamethasone in relapsed or refractory multiple myeloma patients – real world evidence analysis

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          Abstract

          We performed real world evidence (RWE) analysis of daratumumab, lenalidomide and dexamethasone (Dara-Rd) versus lenalidomide and dexamethasone (Rd) treatment in relapsed/refractory multiple myeloma patients (RRMM). In total, 240 RRMM patients were treated with Dara-Rd from 2016 to 2022 outside of clinical trials in all major Czech hematology centers. As a reference, 531 RRMM patients treated with Rd were evaluated. Patients’ data were recorded in the Czech Registry of Monoclonal Gammopathies (RMG). Partial response (PR) or better response (ORR) was achieved in significantly more patients in Dara-Rd than in Rd group (91.2% vs. 69.9%; p < 0.001). The median progression free survival (PFS) was 26.9 months in the Dara-Rd and 12.8 months in the Rd group (p < 0.001). Median overall survival (OS) was not reached in the Dara-Rd compared to 27.2 months in the Rd group (p = 0.023). In patients with 1–3 previous treatment lines, there was significant PFS benefit of Dara-Rd compared to Rd (median PFS not reached vs. 13.2 months; p < 0.001). In patients with > 3 previous treatment lines, there was no significant PFS benefit of Dara-Rd treatment (7.8 months vs. 9.9 months; p = 0.874), similarly in patients refractory to PI + IMIDs (11.5 months vs. 9.2 months; p = 0.376). In RWE conditions, the median PFS in RRMM patients treated with Dara-Rd is shorter when compared to clinical trials. In heavily pretreated RRMM patients, efficacy of Dara-Rd treatment is limited; best possible outcomes of Dara-Rd are achieved in minimally pretreated patients.

          Supplementary Information

          The online version contains supplementary material available at 10.1007/s00277-023-05188-4.

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          Most cited references41

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          Revised International Staging System for Multiple Myeloma: A Report From International Myeloma Working Group.

          The clinical outcome of multiple myeloma (MM) is heterogeneous. A simple and reliable tool is needed to stratify patients with MM. We combined the International Staging System (ISS) with chromosomal abnormalities (CA) detected by interphase fluorescent in situ hybridization after CD138 plasma cell purification and serum lactate dehydrogenase (LDH) to evaluate their prognostic value in newly diagnosed MM (NDMM).
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            Targeting CD38 with Daratumumab Monotherapy in Multiple Myeloma.

            Multiple myeloma cells uniformly overexpress CD38. We studied daratumumab, a CD38-targeting, human IgG1κ monoclonal antibody, in a phase 1-2 trial involving patients with relapsed myeloma or relapsed myeloma that was refractory to two or more prior lines of therapy.
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              Daratumumab depletes CD38+ immune regulatory cells, promotes T-cell expansion, and skews T-cell repertoire in multiple myeloma.

              Daratumumab targets CD38-expressing myeloma cells through a variety of immune-mediated mechanisms (complement-dependent cytotoxicity, antibody-dependent cell-mediated cytotoxicity, and antibody-dependent cellular phagocytosis) and direct apoptosis with crosslinking. These mechanisms may also target nonplasma cells that express CD38, which prompted evaluation of daratumumab's effects on CD38-positive immune subpopulations. Peripheral blood (PB) and bone marrow (BM) from patients with relapsed/refractory myeloma from 2 daratumumab monotherapy studies were analyzed before and during therapy and at relapse. Regulatory B cells and myeloid-derived suppressor cells, previously shown to express CD38, were evaluated for immunosuppressive activity and daratumumab sensitivity in the myeloma setting. A novel subpopulation of regulatory T cells (Tregs) expressing CD38 was identified. These Tregs were more immunosuppressive in vitro than CD38-negative Tregs and were reduced in daratumumab-treated patients. In parallel, daratumumab induced robust increases in helper and cytotoxic T-cell absolute counts. In PB and BM, daratumumab induced significant increases in CD8(+):CD4(+) and CD8(+):Treg ratios, and increased memory T cells while decreasing naïve T cells. The majority of patients demonstrated these broad T-cell changes, although patients with a partial response or better showed greater maximum effector and helper T-cell increases, elevated antiviral and alloreactive functional responses, and significantly greater increases in T-cell clonality as measured by T-cell receptor (TCR) sequencing. Increased TCR clonality positively correlated with increased CD8(+) PB T-cell counts. Depletion of CD38(+) immunosuppressive cells, which is associated with an increase in T-helper cells, cytotoxic T cells, T-cell functional response, and TCR clonality, represents possible additional mechanisms of action for daratumumab and deserves further exploration.
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                Author and article information

                Contributors
                Pour.ludek@fnbrno.cz
                Journal
                Ann Hematol
                Ann Hematol
                Annals of Hematology
                Springer Berlin Heidelberg (Berlin/Heidelberg )
                0939-5555
                1432-0584
                24 April 2023
                24 April 2023
                2023
                : 102
                : 6
                : 1501-1511
                Affiliations
                [1 ]Department of Internal Medicine, Hematology and Oncology, Faculty of Medicine, University Hospital Brno, Masaryk University, Brno, Czech Republic
                [2 ]GRID grid.411798.2, ISNI 0000 0000 9100 9940, 1st Medical Department – Clinical Department of Hematology of the First Faculty of Medicine, , General Teaching Hospital Charles University, ; Prague, Czech Republic
                [3 ]GRID grid.412539.8, ISNI 0000 0004 0609 2284, 4th Department of Medicine – Hematology, Faculty of Medicine, , Charles University Hospital, ; Hradec Kralove, Czech Republic
                [4 ]Department of Hemato-Oncology, Faculty of Medicine and Dentistry, University Hospital Olomouc, Palacky University Olomouc, Olomouc, Czech Republic
                [5 ]GRID grid.412684.d, ISNI 0000 0001 2155 4545, Department of Hematooncology, Faculty of Medicine, , University Hospital Ostrava, University of Ostrava, ; Ostrava, Czech Republic
                [6 ]GRID grid.412694.c, ISNI 0000 0000 8875 8983, Hematology and Oncology Department, , Charles University Hospital, ; Pilsen, Czech Republic
                [7 ]GRID grid.412819.7, ISNI 0000 0004 0611 1895, Department of Internal Medicine and Hematology, , University Hospital Kralovske Vinohrady, ; Prague, Czech Republic
                [8 ]Institute of Biostatistics and Analyses, Ltd., Brno, Czech Republic
                [9 ]GRID grid.10267.32, ISNI 0000 0001 2194 0956, Babak Myeloma Group, Department of Pathophysiology, Faculty of Medicine, , Masaryk University, ; Brno, Czech Republic
                Author information
                http://orcid.org/0000-0002-7194-6771
                Article
                5188
                10.1007/s00277-023-05188-4
                10182121
                37088816
                afacdb3c-207e-40c7-8d08-5ac88fe9727a
                © The Author(s) 2023

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 14 February 2023
                : 16 March 2023
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100003243, Ministerstvo Zdravotnictví Ceské Republiky;
                Award ID: NU21-03-00076
                Award ID: FNBr
                Award ID: 65269705
                Award Recipient :
                Funded by: European Union
                Award ID: LX22NPO5102
                Award Recipient :
                Funded by: Masaryk University
                Categories
                Original Article
                Custom metadata
                © Springer-Verlag GmbH Germany, part of Springer Nature 2023

                Hematology
                multiple myeloma,treatment,response rate,relapse
                Hematology
                multiple myeloma, treatment, response rate, relapse

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