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

Authors :
Kwon M
Iacoboni G
Reguera JL
Corral LL
Morales RH
Ortiz-Maldonado V
Guerreiro M
Caballero AC
Domínguez MLG
Pina JMS
Mussetti A
Sancho JM
Bastos-Oreiro M
Catala E
Delgado J
Henriquez HL
Sanz J
Calbacho M
Bailén R
Carpio C
Ribera JM
Sureda A
Briones J
Hernandez-Boluda JC
Cebrián NM
Martin JLD
Martín A
Barba P
Source :
Haematologica [Haematologica] 2023 Jan 01; Vol. 108 (1), pp. 110-121. Date of Electronic Publication: 2023 Jan 01.
Publication Year :
2023

Abstract

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 lymphodepletion. 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.

Details

Language :
English
ISSN :
1592-8721
Volume :
108
Issue :
1
Database :
MEDLINE
Journal :
Haematologica
Publication Type :
Academic Journal
Accession number :
35770532
Full Text :
https://doi.org/10.3324/haematol.2022.280805