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Macrophage activation syndrome-like in multiple myeloma patients treated with the academic CAR-T against BCMA ARI0002h
by
Cabañas, Valentín
, Urbano-Ispizua, Álvaro
, López-Corral, Lucía
, Munárriz, Daniel
, Fernández de Larrea, Carlos
, Varea, Sara
, Mateos, María-Victoria
, Martínez-Cibrián, Núria
, Moraleda, José María
, De la Calle, Verónica González
, Oliver-Caldés, Aina
, López-Muñoz, Nieves
, Reguera, Juan Luis
, González-Navarro, Europa Azucena
, Martínez-López, Joaquín
, Arnaldos-Pérez, Cristina
, Rodríguez-Otero, Paula
, Rodríguez-Lobato, Luis Gerardo
, Delgado, Julio
, Ponce, Juan Carlos
, Tovar, Natalia
, Martín, Ana África
, Guillen, Elena
in
Adult
/ Aged
/ Aged, 80 and over
/ anti-BCMA CAR T
/ B-Cell Maturation Antigen - antagonists & inhibitors
/ B-Cell Maturation Antigen - immunology
/ Cell activation
/ Chimeric antigen receptors
/ Clinical trials
/ Cytokines
/ Female
/ Ferritin
/ Humans
/ Hypertriglyceridemia
/ IEC-HS
/ Immunology
/ immunotherapy
/ Immunotherapy, Adoptive - adverse effects
/ Immunotherapy, Adoptive - methods
/ Lymphocytes
/ Lymphocytes B
/ Lymphocytes T
/ Lymphoma
/ Macrophage Activation Syndrome - diagnosis
/ Macrophage Activation Syndrome - etiology
/ Macrophage Activation Syndrome - immunology
/ Macrophages
/ Male
/ MAS-like syndrome
/ Medical prognosis
/ Middle Aged
/ Multiple myeloma
/ Multiple Myeloma - immunology
/ Multiple Myeloma - mortality
/ Multiple Myeloma - therapy
/ myeloma
/ Neurotoxicity
/ Patients
/ Receptors, Chimeric Antigen - immunology
/ Retrospective Studies
/ Risk factors
/ Toxicity
/ Treatment Outcome
2025
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Macrophage activation syndrome-like in multiple myeloma patients treated with the academic CAR-T against BCMA ARI0002h
by
Cabañas, Valentín
, Urbano-Ispizua, Álvaro
, López-Corral, Lucía
, Munárriz, Daniel
, Fernández de Larrea, Carlos
, Varea, Sara
, Mateos, María-Victoria
, Martínez-Cibrián, Núria
, Moraleda, José María
, De la Calle, Verónica González
, Oliver-Caldés, Aina
, López-Muñoz, Nieves
, Reguera, Juan Luis
, González-Navarro, Europa Azucena
, Martínez-López, Joaquín
, Arnaldos-Pérez, Cristina
, Rodríguez-Otero, Paula
, Rodríguez-Lobato, Luis Gerardo
, Delgado, Julio
, Ponce, Juan Carlos
, Tovar, Natalia
, Martín, Ana África
, Guillen, Elena
in
Adult
/ Aged
/ Aged, 80 and over
/ anti-BCMA CAR T
/ B-Cell Maturation Antigen - antagonists & inhibitors
/ B-Cell Maturation Antigen - immunology
/ Cell activation
/ Chimeric antigen receptors
/ Clinical trials
/ Cytokines
/ Female
/ Ferritin
/ Humans
/ Hypertriglyceridemia
/ IEC-HS
/ Immunology
/ immunotherapy
/ Immunotherapy, Adoptive - adverse effects
/ Immunotherapy, Adoptive - methods
/ Lymphocytes
/ Lymphocytes B
/ Lymphocytes T
/ Lymphoma
/ Macrophage Activation Syndrome - diagnosis
/ Macrophage Activation Syndrome - etiology
/ Macrophage Activation Syndrome - immunology
/ Macrophages
/ Male
/ MAS-like syndrome
/ Medical prognosis
/ Middle Aged
/ Multiple myeloma
/ Multiple Myeloma - immunology
/ Multiple Myeloma - mortality
/ Multiple Myeloma - therapy
/ myeloma
/ Neurotoxicity
/ Patients
/ Receptors, Chimeric Antigen - immunology
/ Retrospective Studies
/ Risk factors
/ Toxicity
/ Treatment Outcome
2025
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Macrophage activation syndrome-like in multiple myeloma patients treated with the academic CAR-T against BCMA ARI0002h
by
Cabañas, Valentín
, Urbano-Ispizua, Álvaro
, López-Corral, Lucía
, Munárriz, Daniel
, Fernández de Larrea, Carlos
, Varea, Sara
, Mateos, María-Victoria
, Martínez-Cibrián, Núria
, Moraleda, José María
, De la Calle, Verónica González
, Oliver-Caldés, Aina
, López-Muñoz, Nieves
, Reguera, Juan Luis
, González-Navarro, Europa Azucena
, Martínez-López, Joaquín
, Arnaldos-Pérez, Cristina
, Rodríguez-Otero, Paula
, Rodríguez-Lobato, Luis Gerardo
, Delgado, Julio
, Ponce, Juan Carlos
, Tovar, Natalia
, Martín, Ana África
, Guillen, Elena
in
Adult
/ Aged
/ Aged, 80 and over
/ anti-BCMA CAR T
/ B-Cell Maturation Antigen - antagonists & inhibitors
/ B-Cell Maturation Antigen - immunology
/ Cell activation
/ Chimeric antigen receptors
/ Clinical trials
/ Cytokines
/ Female
/ Ferritin
/ Humans
/ Hypertriglyceridemia
/ IEC-HS
/ Immunology
/ immunotherapy
/ Immunotherapy, Adoptive - adverse effects
/ Immunotherapy, Adoptive - methods
/ Lymphocytes
/ Lymphocytes B
/ Lymphocytes T
/ Lymphoma
/ Macrophage Activation Syndrome - diagnosis
/ Macrophage Activation Syndrome - etiology
/ Macrophage Activation Syndrome - immunology
/ Macrophages
/ Male
/ MAS-like syndrome
/ Medical prognosis
/ Middle Aged
/ Multiple myeloma
/ Multiple Myeloma - immunology
/ Multiple Myeloma - mortality
/ Multiple Myeloma - therapy
/ myeloma
/ Neurotoxicity
/ Patients
/ Receptors, Chimeric Antigen - immunology
/ Retrospective Studies
/ Risk factors
/ Toxicity
/ Treatment Outcome
2025
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Macrophage activation syndrome-like in multiple myeloma patients treated with the academic CAR-T against BCMA ARI0002h
Journal Article
Macrophage activation syndrome-like in multiple myeloma patients treated with the academic CAR-T against BCMA ARI0002h
2025
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Overview
Chimeric antigen receptor T-cell (CAR-T) therapy targeting B-cell maturation antigen (BCMA) has revolutionized multiple myeloma treatment (MM). However, managing its immune-mediated adverse events, particularly macrophage activation syndrome-
(MAS-
), remains challenging due to underreporting.
This multicentre, retrospective, analytical study evaluated MM patients treated with the anti-BCMA academic product ARI0002h. MAS-
was defined using the University of California San Francisco (UCSF) consensus criteria. Primary endpoints included baseline characteristics, predictive factors, and survival outcomes associated with MAS-
.
Of 80 patients, 12 (15%) met the UCSF criteria for MAS-
. These patients presented higher ISS scores (ISS III: 54.5% vs. 15.2%;
= 0.006), elevated serum monoclonal components (31.3 g/L vs. 6.8 g/L;
= 0.004), and a higher prevalence of extramedullary disease (41.7% vs. 16.2%;
= 0.057). MAS-
typically emerged 9 days post-infusion, with elevated ferritin, followed by LDH (median 11.5 days) and hypofibrinogenemia (median 14 days). One-third of patients met all UCSF criteria, and all exhibited hypertriglyceridemia, hypertransaminasemia, and cytopenias. Histopathological examination was positive in 63% of evaluated patients. Patients who developed MAS-
had poorer responses (CR: 25% vs. 68%; p = 0.008) and shorter median PFS and OS (7 months vs. 21.4 months and 18 months vs. not reached, respectively; p = 0.004). Those meeting all UCSF criteria had even inferior outcomes.
MAS-
is associated with poorer responses, reduced PFS and OS, especially in patients meeting all UCSF criteria. High tumour burden, including elevated monoclonal component, high ISS and extramedullary disease, seems to contribute to MAS-
development.
Publisher
Frontiers Media SA,Frontiers Media S.A
Subject
/ Aged
/ B-Cell Maturation Antigen - antagonists & inhibitors
/ B-Cell Maturation Antigen - immunology
/ Female
/ Ferritin
/ Humans
/ IEC-HS
/ Immunotherapy, Adoptive - adverse effects
/ Immunotherapy, Adoptive - methods
/ Lymphoma
/ Macrophage Activation Syndrome - diagnosis
/ Macrophage Activation Syndrome - etiology
/ Macrophage Activation Syndrome - immunology
/ Male
/ Multiple Myeloma - immunology
/ Multiple Myeloma - mortality
/ myeloma
/ Patients
/ Receptors, Chimeric Antigen - immunology
/ Toxicity
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