Results of ARI-0001 CART19 Cells in Patients With Chronic Lymphocytic Leukemia and Richter's Transformation

CART19 cells are emerging as an alternative therapy for patients with chronic lymphocytic leukemia (CLL). Here we report the outcome of nine consecutive patients with CLL treated with ARI-0001 CART19 cells, six of them with Richter’s transformation (RT). One patient with RT never received therapy. T...

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Detalles Bibliográficos
Autores: Ortiz-Maldonado Gibson, Valentín, Frigola, Gerard, Español Rego, Marta, Balagué, Olga, Martínez Cibrian, Nuria, Magnano, Laura, Giné Soca, Eva, Pascal i Capdevila, Mariona, Correa, Juan G., Martínez-Roca, Alexandra, Cid Vidal, Joan, Lozano Molero, Miguel, Villamor i Casas, Neus, Benítez-Ribas, Daniel, Esteve Comas, Jordi, López Guillermo, Armando, Campo Güerri, Elias, Urbano Ispizua, Álvaro, Juan, Manel, Delgado, Julio (Delgado González)
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2022
País:España
Institución:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repositorio:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:2445/197660
Acceso en línea:https://hdl.handle.net/2445/197660
Access Level:acceso abierto
Palabra clave:Leucèmia limfocítica crònica
Teràpia cel·lular
Chronic lymphocytic leukemia
Cellular therapy
Descripción
Sumario:CART19 cells are emerging as an alternative therapy for patients with chronic lymphocytic leukemia (CLL). Here we report the outcome of nine consecutive patients with CLL treated with ARI-0001 CART19 cells, six of them with Richter’s transformation (RT). One patient with RT never received therapy. The cytokine release syndrome rate was 87.5% (12.5% grade ≥3). Neurotoxicity was not observed in any patient. All patients experienced absolute B-cell aplasia, and seven (87.5%) responded to therapy. With a median follow-up of 5.6 months, two patients with RT experienced a CD19-negative relapse. In conclusion, ARI-0001 cell therapy was feasible, safe, and effective in patients with high risk CLL or RT