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Axicabtagene ciloleucel compared to tisagenlecleucel for the treatment of aggressive B-cell lymphoma

Axicabtagene ciloleucel (axi-cel) and tisagenlecleucel (tisa-cel) are CD19-targeted chimeric antigen receptor (CAR) T cells approved for relapsed/refractory (R/R) large B-cell lymphoma (LBCL). We performed a retrospective study to evaluate safety and efficacy of axi-cel and tisa-cel outside the sett...

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Autores principales: Kwon, Mi, Iacoboni, Gloria, Reguera, Juan Luis, Corral, Lucía López, Morales, Rafael Hernani, Ortiz-Maldonado, Valentín, Guerreiro, Manuel, Caballero, Ana Carolina, Domínguez, María Luisa Guerra, Pina, Jose Maria Sanchez, Mussetti, Alberto, Sancho, Juan Manuel, Bastos-Oreiro, Mariana, Catala, Eva, Delgado, Javier, Henriquez, Hugo Luzardo, Sanz, Jaime, Calbacho, María, Bailén, Rebeca, Carpio, Cecilia, Ribera, Jose Maria, Sureda, Anna, Briones, Javier, Hernandez-Boluda, Juan Carlos, Cebrián, Nuria Martínez, Martin, Jose Luis Diez, Martín, Alejandro, Barba, Pere
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Fondazione Ferrata Storti 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9827173/
https://www.ncbi.nlm.nih.gov/pubmed/35770532
http://dx.doi.org/10.3324/haematol.2022.280805
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author Kwon, Mi
Iacoboni, Gloria
Reguera, Juan Luis
Corral, Lucía López
Morales, Rafael Hernani
Ortiz-Maldonado, Valentín
Guerreiro, Manuel
Caballero, Ana Carolina
Domínguez, María Luisa Guerra
Pina, Jose Maria Sanchez
Mussetti, Alberto
Sancho, Juan Manuel
Bastos-Oreiro, Mariana
Catala, Eva
Delgado, Javier
Henriquez, Hugo Luzardo
Sanz, Jaime
Calbacho, María
Bailén, Rebeca
Carpio, Cecilia
Ribera, Jose Maria
Sureda, Anna
Briones, Javier
Hernandez-Boluda, Juan Carlos
Cebrián, Nuria Martínez
Martin, Jose Luis Diez
Martín, Alejandro
Barba, Pere
author_facet Kwon, Mi
Iacoboni, Gloria
Reguera, Juan Luis
Corral, Lucía López
Morales, Rafael Hernani
Ortiz-Maldonado, Valentín
Guerreiro, Manuel
Caballero, Ana Carolina
Domínguez, María Luisa Guerra
Pina, Jose Maria Sanchez
Mussetti, Alberto
Sancho, Juan Manuel
Bastos-Oreiro, Mariana
Catala, Eva
Delgado, Javier
Henriquez, Hugo Luzardo
Sanz, Jaime
Calbacho, María
Bailén, Rebeca
Carpio, Cecilia
Ribera, Jose Maria
Sureda, Anna
Briones, Javier
Hernandez-Boluda, Juan Carlos
Cebrián, Nuria Martínez
Martin, Jose Luis Diez
Martín, Alejandro
Barba, Pere
author_sort Kwon, Mi
collection PubMed
description Axicabtagene ciloleucel (axi-cel) and tisagenlecleucel (tisa-cel) are CD19-targeted chimeric antigen receptor (CAR) T cells approved for relapsed/refractory (R/R) large B-cell lymphoma (LBCL). We performed a retrospective study to evaluate safety and efficacy of axi-cel and tisa-cel outside the setting of a clinical trial. Data from consecutive patients with R/R LBCL who underwent apheresis for axi-cel or tisa-cel were retrospectively collected from 12 Spanish centers. A total of 307 patients underwent apheresis for axi-cel (n=152) and tisa-cel (n=155) from November 2018 to August 2021, of which 261 (85%) received a CAR T infusion (88% and 82%, respectively). Median time from apheresis to infusion was 41 days for axi-cel and 52 days for tisa-cel (P=0.006). None of the baseline characteristics were significantly different between both cohorts. Both cytokine release syndrome and neurologic events (NE) were more frequent in the axi-cel group (88% vs. 73%, P=0.003, and 42% vs. 16%, P<0.001, respectively). Infections in the first 6 months post-infusion were also more common in patients treated with axi-cel (38% vs. 25%, P=0.033). Non-relapse mortality was not significantly different between the axi-cel and tisa-cel groups (7% and 4%, respectively, P=0.298). With a median follow-up of 9.2 months, median PFS and OS were 5.9 and 3 months, and 13.9 and 11.2 months for axi-cel and tisa-cel, respectively. The 12-month PFS and OS for axi-cel and tisa-cel were 41% and 33% (P=0.195), 51% and 47% (P=0.191), respectively. Factors associated with lower OS in the multivariate analysis were increased lactate dehydrogenase, ECOG ≥2 and progressive disease before lympho-depletion. Safety and efficacy results in our real-world experience were comparable with those reported in the pivotal trials. Patients treated with axi-cel experienced more toxicity but similar non-relapse mortality compared with those receiving tisa-cel. Efficacy was not significantly different between both products.
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spelling pubmed-98271732023-01-20 Axicabtagene ciloleucel compared to tisagenlecleucel for the treatment of aggressive B-cell lymphoma Kwon, Mi Iacoboni, Gloria Reguera, Juan Luis Corral, Lucía López Morales, Rafael Hernani Ortiz-Maldonado, Valentín Guerreiro, Manuel Caballero, Ana Carolina Domínguez, María Luisa Guerra Pina, Jose Maria Sanchez Mussetti, Alberto Sancho, Juan Manuel Bastos-Oreiro, Mariana Catala, Eva Delgado, Javier Henriquez, Hugo Luzardo Sanz, Jaime Calbacho, María Bailén, Rebeca Carpio, Cecilia Ribera, Jose Maria Sureda, Anna Briones, Javier Hernandez-Boluda, Juan Carlos Cebrián, Nuria Martínez Martin, Jose Luis Diez Martín, Alejandro Barba, Pere Haematologica Article - Cell Therapy & Immunotherapy Axicabtagene ciloleucel (axi-cel) and tisagenlecleucel (tisa-cel) are CD19-targeted chimeric antigen receptor (CAR) T cells approved for relapsed/refractory (R/R) large B-cell lymphoma (LBCL). We performed a retrospective study to evaluate safety and efficacy of axi-cel and tisa-cel outside the setting of a clinical trial. Data from consecutive patients with R/R LBCL who underwent apheresis for axi-cel or tisa-cel were retrospectively collected from 12 Spanish centers. A total of 307 patients underwent apheresis for axi-cel (n=152) and tisa-cel (n=155) from November 2018 to August 2021, of which 261 (85%) received a CAR T infusion (88% and 82%, respectively). Median time from apheresis to infusion was 41 days for axi-cel and 52 days for tisa-cel (P=0.006). None of the baseline characteristics were significantly different between both cohorts. Both cytokine release syndrome and neurologic events (NE) were more frequent in the axi-cel group (88% vs. 73%, P=0.003, and 42% vs. 16%, P<0.001, respectively). Infections in the first 6 months post-infusion were also more common in patients treated with axi-cel (38% vs. 25%, P=0.033). Non-relapse mortality was not significantly different between the axi-cel and tisa-cel groups (7% and 4%, respectively, P=0.298). With a median follow-up of 9.2 months, median PFS and OS were 5.9 and 3 months, and 13.9 and 11.2 months for axi-cel and tisa-cel, respectively. The 12-month PFS and OS for axi-cel and tisa-cel were 41% and 33% (P=0.195), 51% and 47% (P=0.191), respectively. Factors associated with lower OS in the multivariate analysis were increased lactate dehydrogenase, ECOG ≥2 and progressive disease before lympho-depletion. Safety and efficacy results in our real-world experience were comparable with those reported in the pivotal trials. Patients treated with axi-cel experienced more toxicity but similar non-relapse mortality compared with those receiving tisa-cel. Efficacy was not significantly different between both products. Fondazione Ferrata Storti 2022-06-30 /pmc/articles/PMC9827173/ /pubmed/35770532 http://dx.doi.org/10.3324/haematol.2022.280805 Text en Copyright© 2023 Ferrata Storti Foundation https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution Noncommercial License (by-nc 4.0) which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Article - Cell Therapy & Immunotherapy
Kwon, Mi
Iacoboni, Gloria
Reguera, Juan Luis
Corral, Lucía López
Morales, Rafael Hernani
Ortiz-Maldonado, Valentín
Guerreiro, Manuel
Caballero, Ana Carolina
Domínguez, María Luisa Guerra
Pina, Jose Maria Sanchez
Mussetti, Alberto
Sancho, Juan Manuel
Bastos-Oreiro, Mariana
Catala, Eva
Delgado, Javier
Henriquez, Hugo Luzardo
Sanz, Jaime
Calbacho, María
Bailén, Rebeca
Carpio, Cecilia
Ribera, Jose Maria
Sureda, Anna
Briones, Javier
Hernandez-Boluda, Juan Carlos
Cebrián, Nuria Martínez
Martin, Jose Luis Diez
Martín, Alejandro
Barba, Pere
Axicabtagene ciloleucel compared to tisagenlecleucel for the treatment of aggressive B-cell lymphoma
title Axicabtagene ciloleucel compared to tisagenlecleucel for the treatment of aggressive B-cell lymphoma
title_full Axicabtagene ciloleucel compared to tisagenlecleucel for the treatment of aggressive B-cell lymphoma
title_fullStr Axicabtagene ciloleucel compared to tisagenlecleucel for the treatment of aggressive B-cell lymphoma
title_full_unstemmed Axicabtagene ciloleucel compared to tisagenlecleucel for the treatment of aggressive B-cell lymphoma
title_short Axicabtagene ciloleucel compared to tisagenlecleucel for the treatment of aggressive B-cell lymphoma
title_sort axicabtagene ciloleucel compared to tisagenlecleucel for the treatment of aggressive b-cell lymphoma
topic Article - Cell Therapy & Immunotherapy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9827173/
https://www.ncbi.nlm.nih.gov/pubmed/35770532
http://dx.doi.org/10.3324/haematol.2022.280805
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