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https://hdl.handle.net/2445/219914
Title: | The academic point-of-care anti-CD19 chimeric antigen receptor T-cell product varnimcabtagene autoleucel (ARI-0001 cells) shows efficacy and safety in the treatment of relapsed/refractory B-cell non-Hodgkin lymphoma |
Author: | Martínez Cibrián, Núria Ortiz Maldonado, Valentín Español Rego, Marta Blázquez, Andrea Cid, Joan Lozano, Miquel Magnano, Laura Giné Soca, Eva Correa, Juan G. Mozas, Pablo Rodríguez Lobato, Luis Gerardo Rivero, Andrea Montoro Lorite, Mercedes Ayora, Pilar Navarro, Sergio Alserawan, Leticia González Navarro, Europa Azucena Castellà, Maria Sánchez Castañón, María Cabezón, Raquel Benítez Ribas, Daniel Setoaín, Xavier Rodríguez, Sonia Brillembourg, Helena Varea, Sara Olesti Muñoz, Eulàlia Guillén, Elena Sáez Peñataro, Joaquín Fernández De Larrea, Carlos López Guillermo, Armando Pascal, Mariona Urbano Ispizua, Álvaro Juan, Manel Delgado, Julio |
Keywords: | Antígens Immunoteràpia Limfomes Antigens Immunotheraphy Lymphomas |
Issue Date: | Feb-2024 |
Publisher: | John Wiley & Sons |
Abstract: | Varnimcabtagene autoleucel (var-cel) is an academic anti-CD19 chimeric antigen receptor (CAR) product used for the treatment of non-Hodgkin lymphoma (NHL) in the CART19-BE-01 trial. Here we report updated outcomes of patients with NHL treated with var-cel. B-cell recovery was compared with patients with acute lymphoblastic leukaemia (ALL). Forty-five patients with NHL were treated. Cytokine release syndrome (any grade) occurred in 84% of patients (4% grade ≥3) and neurotoxicity in 7% (2% grade ≥3). The objective response rate was 73% at Day +100, and the 3-year duration of response was 56%. The 3-year progression-free and overall survival were 40% and 52% respectively. High lactate dehydrogenase was the only covariate with an impact on progression-free survival. The 3-year incidence of B-cell recovery was lower in patients with NHL compared to ALL (25% vs. 60%). In conclusion, in patients with NHL, the toxicity of var-cel was manageable, while B-cell recovery was significantly prolonged compared to ALL. This trial was registered as NCT03144583. |
Note: | Reproducció del document publicat a: https://doi.org/10.1111/bjh.19170 |
It is part of: | British Journal of Haematology, 2024, vol. 204, num.2, p. 525-533 |
URI: | https://hdl.handle.net/2445/219914 |
Related resource: | https://doi.org/10.1111/bjh.19170 |
ISSN: | 0007-1048 |
Appears in Collections: | Articles publicats en revistes (Medicina) Articles publicats en revistes (IDIBAPS: Institut d'investigacions Biomèdiques August Pi i Sunyer) |
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