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DOI 10.1016/j.jtct.2025.01.001

Медицинская библиотека · Transplantation and cellular therapy · 2025

Reduced Chimeric Antigen Receptor T Cell Expansion Postinfusion Is Associated with Poor Survival in Patients with Large B Cell Lymphoma after Two or More Therapies.

Abadir Edward, Wayte Rebecca, Li Wenlong, Gupta Sachin, Yang Shihong, Reaiche Elizabeth, Debosz Katrina, Anderson Emily, Favaloro James, Aklilu Esther, Brown Christina, Bryant Christian, Dunkley Scott, McCulloch Derek, Larsen Stephen, Rasko John E J, Vanguru Vinay, Ho P Joy

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Аннотация

CD19-directed chimeric antigen receptor T cell (CAR-T) therapy is now standard of care for relapsed/refractory large B cell non-Hodgkin lymphoma. Despite good overall response rates, many patients still experience disease progression and therefore it is important to predict those at risk of relapse following CAR-T therapy. We performed a prospective study using a flow cytometry assay at a single treatment center to assess early CAR T cell expansion in vivo 6 to 9 days after CAR T cell infusion. Early CAR T cell expansion was used in conjunction with additional clinical risk factors to identify those at greater risk of relapse or treatment failure. Forty-four patients treated with commercial CD19-directed CAR-T therapy were included in the study, with a median follow-up of 306 days. CAR T cell expansion of >30 cells/μL was associated with a lower risk of disease progression or death (hazard ratio, 0.34; P = .048), but did not correlate with the risk of death alone. Patients who had poor early CAR T cell expansion (<30 cells/μL) in addition to high lactate dehydrogenase (LDH) had significantly lower median progression-free survival and overall survival. High LDH level alone was not a statistically significant risk factor for death or disease progression, and thus the interaction between CAR T cell expansion and this clinical risk factor may be important in predicting response. The mean CAR T cell count was higher in patients with grade 2 to 4 cytokine release syndrome (CRS) compared to those with grade 0 to 1 CRS (54.9 cells/μL versus 25.5 cells/μL; P = .01). The methodology of this assay is easily reproducible outside of a clinical trial, allowing for real-life implementation in clinical settings. This study suggests that early assessment of CAR T cell expansion can assist in identifying patients with poor overall survival who may benefit from early intervention or more intensive monitoring.

Для цитирования: Abadir Edward, Wayte Rebecca, Li Wenlong, Gupta Sachin, Yang Shihong, Reaiche Elizabeth, Debosz Katrina, Anderson Emily, Favaloro James, Aklilu Esther, Brown Christina, Bryant Christian, Dunkley Scott, McCulloch Derek, Larsen Stephen, Rasko John E J, Vanguru Vinay, Ho P Joy. Reduced Chimeric Antigen Receptor T Cell Expansion Postinfusion Is Associated with Poor Survival in Patients with Large B Cell Lymphoma after Two or More Therapies.. Transplantation and cellular therapy. 2025. DOI: 10.1016/j.jtct.2025.01.001.

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