Immuno-engineering and Cellular Therapies
Iñaki Ortiz de Landazuri, n/a
Immunology Department, Centre de Diagnòstic Biomèdic, Hospital Clínic de Barcelona, Barcelona, Spain
Barcelona, Catalonia, Spain
Guillermo Muñoz Sánchez, n/a
Immunology Department, Centre de Diagnòstic Biomèdic, Hospital Clínic of Barcelona, Barcelona, Spain.
Barcelona, Catalonia, Spain
Valentín Ortiz Maldonado, n/a
Hematology Department, ICMHO, Hospital Clínic de Barcelona, Barcelona, Spain
Barcelona, Catalonia, Spain
Aina Oliver-Caldes, n/a
Hematology Department, ICMHO, Hospital Clínic de Barcelona, Barcelona, Spain
Barcelona, Catalonia, Spain
Victor Bolaño, n/a
Immunology Department, Centre de Diagnòstic Biomèdic, Hospital Clínic de Barcelona, Barcelona, Spain
Barcelona, Catalonia, Spain
Marta Español Rego, n/a
Immunology Department, Centre de Diagnòstic Biomèdic, Hospital Clínic de Barcelona, Barcelona, Spain
Barcelona, Catalonia, Spain
Laura Naranjo, n/a
Immunology Department, Centre de Diagnòstic Biomèdic, Hospital Clínic de Barcelona, Barcelona, Spain
Barcelona, Catalonia, Spain
Julio Delgado, n/a
Hematology Department, ICMHO, Hospital Clínic de Barcelona, Barcelona, Spain
Barcelona, Catalonia, Spain
Carlos Fernández de Larrea, n/a
Hematology Department, ICMHO, Hospital Clínic de Barcelona, Barcelona, Spain
Barcelona, Catalonia, Spain
Susana Rives, n/a
Department of Pediatric Hematology and Oncology, Hospital Sant Joan de Déu Barcelona, Barcelona
Barcelona, Catalonia, Spain
Yolanda Blanco, n/a
Neurology Department, ICN, Hospital Clínic de Barcelona, Barcelona, Spain
Barcelona, Catalonia, Spain
Albert Saiz, n/a
Neurology Department, ICN, Hospital Clínic de Barcelona, Barcelona, Spain
Barcelona, Catalonia, Spain
Mariona Pascal, n/a
Department of Immunology, Centre de Diagnòstic Biomèdic, Hospital Clínic of Barcelona, Barcelona, Spain
Barcelona, Catalonia, Spain
Manel Juan, n/a
Head of Department
Department of Immunology, Centre de Diagnòstic Biomèdic, Hospital Clínic of Barcelona, Barcelona, Spain.
Barcelona, Catalonia, Spain
Raquel Ruiz-García, n/a
Immunology Department, Centre de Diagnòstic Biomèdic, Hospital Clínic de Barcelona, Barcelona, Spain
Barcelona, Catalonia, Spain
The Immune effector Cell-Associated Neurotoxicity Syndrome (ICANS) is an adverse event associated to Chimeric Antigen Receptor (CAR) T-cell therapy. Neurofilament light chain (NfL) levels have been proposed as a biomarker of neuroinflammation. We hypothesize that NfL could be employed as a biomarker of ICANS risk and severity in CAR T-cell therapy.
We retrospectively measured serum or plasma NfL levels in a cohort of 29 patients who received CAR T-cells against CD19 (n=24) or BCMA (n=5), and 53 age matched healthy donors (HD). Fifteen patients presented ICANS of any grade. Blood samples were obtained at pre, intra and post ICANS episodes in ICANS study group; and at day 0, +7 and +28 after CAR T-cell infusion in patients without ICANS (NO-ICANS).
Both ICANS and NO-ICANS showed higher levels of NfL in comparison to HD prior to CAR T-cell infusion (median: 36.65pg/mL; 52.84pg/mL; 14.96pg/mL).
Grade 3-4 ICANS and grade 1-2 ICANS had a NfL mean of 57.2pg/mL and 28.5pg/mL during episodes, respectively; while NO-ICANS showed a mean of 43.6pg/mL at day+7. Significant differences comparing grade 3-4, 1-2 grade ICANS and NO-ICANS were not observed.
Differences in NfL levels between ICANS (47pg/mL) and NO-ICANS (53.5pg/mL) were not detected post ICANS resolution and at day+28, respectively.
High baseline NfL levels were present in both ICANS and NO-ICANS groups before CAR-T cell therapy. Differences in NfL levels were not observed in patients with ICANS of any grade compared to NO-ICANS group. NfL levels may not help to assess ICANS risk or severity in our cohort.