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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...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Fondazione Ferrata Storti
2022
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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. |
format | Online Article Text |
id | pubmed-9827173 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Fondazione Ferrata Storti |
record_format | MEDLINE/PubMed |
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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