Open AccessAxicabtagene ciloleucel compared to tisagenlecleucel for the treatment of aggressive B-cell lymphoma
Author(s) -
Mi Kwon,
Gloria Iacoboni,
Juan Luís Reguera,
Lucía López Corral,
Rafael Hernani,
Valentín OrtizMaldonado,
Manuel Guerreiro,
A Caballero,
María Luisa Guerra Domínguez,
José María Sánchez Pina,
Alberto Mussetti,
Juan Manuel Sancho,
Mariana BastosOreiro,
Eva Catalá,
Javier Delgado,
H. Luzardo Henriquez,
Jaime Sanz,
María Calbacho,
Rebeca Bailén,
Cecilia Carpio,
Jose Maria Ribera,
Anna Sureda,
Javier Briones,
Juan Carlos HernándezBoluda,
Nuria Martínez Cebrián,
José Luis Díez Martín,
Alejandro Martı́n,
Pere Barba
Publication year - 2022
Publication title -
haematologica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.782
H-Index - 142
eISSN - 1592-8721
pISSN - 0390-6078
DOI - 10.3324/haematol.2022.280805
Subject(s) - medicine , apheresis , cytokine release syndrome , refractory (planetary science) , lymphoma , gastroenterology , chimeric antigen receptor , surgery , immunotherapy , cancer , platelet , physics , astrobiology
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.