Artigo Acesso aberto Revisado por pares

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

2023; Wiley; Volume: 204; Issue: 2 Linguagem: Inglês

10.1111/bjh.19170

ISSN

1365-2141

Autores

Núria Martínez‐Cibrián, Valentín Ortiz‐Maldonado, Marta Español‐Rego, Andrea Blázquez, Joan Cid, Miquel Lozano, Laura Magnano, Eva Giné, Juan Gonzalo Correa, Pablo Mozas, Luis Gerardo Rodríguez‐Lobato, Andrea Rivero, Mercedes Montoro‐Lorite, Pilar Ayora, Sergio Navarro-Velázquez, Letícia Alserawan, Azucena González-Navarro, María Castellà, María Sánchez‐Castañón, Raquel Cabezón, Daniel Benítez‐Ribas, Xavier Setoaín, Sónia Rodríguez, Helena Brillembourg, Sara Varea, Eulàlia Olesti, Elena Guillén, Joaquín Sáez‐Peñataro, Carlos Fernández de Larrea, Armando López‐Guillermo, Mariona Pascal, Álvaro Urbano‐Ispizua, Manel Juan, Julio Delgado,

Tópico(s)

Advancements in Semiconductor Devices and Circuit Design

Resumo

Summary 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.

Referência(s)