TY - JOUR
T1 - Chimeric antigen receptor T-cell infusion for large B-cell lymphoma in complete remission
T2 - a center for international blood and marrow transplant research analysis
AU - Wang, Trent P.
AU - Ahn, Kwang W.
AU - Shadman, Mazyar
AU - Kaur, Manmeet
AU - Ahmed, Nausheen
AU - Bacher, Ulrike
AU - Cerny, Jan
AU - Chen, Andy
AU - Epperla, Narendranath
AU - Frigault, Matthew
AU - Grover, Natalie
AU - Haverkos, Bradley
AU - Hill, Brian
AU - Hossain, Nasheed
AU - Iqbal, Madiha
AU - Jain, Tania
AU - Krem, Maxwell M.
AU - Maakaron, Joseph
AU - Modi, Dipenkumar
AU - Alhaj Moustafa, Muhamad
AU - Riedell, Peter
AU - Savani, Bipin
AU - Sica, R. Alejandro
AU - Sureda, Anna
AU - Wudhikarn, Kitsada
AU - Herrera, Alex F.
AU - Sauter, Craig
AU - Hamadani, Mehdi
AU - Jimenez Jimenez, Antonio
N1 - Publisher Copyright:
© The Author(s), under exclusive licence to Springer Nature Limited 2024.
PY - 2024/7
Y1 - 2024/7
N2 - CD19 CAR T-cell (CAR-T) therapy is commonly administered to patients with relapsed or refractory large B-cell lymphomas (LBCL), but salvage or bridging therapy can sometimes lead to a complete response (CR) prior to infusion. Limited studies have assessed the outcomes of patients infused in CR. A total of 134 patients with LBCL in CR prior to CAR-T infusion were identified from the CIBMTR registry, with median prior lines of therapy of 3 (range 2–9). At two years post-infusion, the probability of progression-free survival was 43.5% (95% CI 34.4–52.8) and the probability of overall survival was 63.8% (95% CI 54.4–72.6). The cumulative incidence rates of non-relapse mortality and relapse/progression at two years were 9.2% (95% CI 4.5–15.4) and 47.3% (95% CI 38.2–56.6), respectively. The rate of grade 3 or higher cytokine release syndrome (CRS) and immune effector cell-associated neurotoxicity syndrome (ICANS) were 2.2% and 8.2%, respectively. In summary, CAR-T in heavily pretreated patients with LBCL who are in CR following two or more lines of prior therapy demonstrate that a subset of patients may remain free of progression at two years. Additionally, the toxicity profile was impressive with very low rates of grade 3 CRS and ICANS.
AB - CD19 CAR T-cell (CAR-T) therapy is commonly administered to patients with relapsed or refractory large B-cell lymphomas (LBCL), but salvage or bridging therapy can sometimes lead to a complete response (CR) prior to infusion. Limited studies have assessed the outcomes of patients infused in CR. A total of 134 patients with LBCL in CR prior to CAR-T infusion were identified from the CIBMTR registry, with median prior lines of therapy of 3 (range 2–9). At two years post-infusion, the probability of progression-free survival was 43.5% (95% CI 34.4–52.8) and the probability of overall survival was 63.8% (95% CI 54.4–72.6). The cumulative incidence rates of non-relapse mortality and relapse/progression at two years were 9.2% (95% CI 4.5–15.4) and 47.3% (95% CI 38.2–56.6), respectively. The rate of grade 3 or higher cytokine release syndrome (CRS) and immune effector cell-associated neurotoxicity syndrome (ICANS) were 2.2% and 8.2%, respectively. In summary, CAR-T in heavily pretreated patients with LBCL who are in CR following two or more lines of prior therapy demonstrate that a subset of patients may remain free of progression at two years. Additionally, the toxicity profile was impressive with very low rates of grade 3 CRS and ICANS.
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U2 - 10.1038/s41375-024-02242-6
DO - 10.1038/s41375-024-02242-6
M3 - Article
C2 - 38750138
AN - SCOPUS:85193054339
SN - 0887-6924
VL - 38
SP - 1564
EP - 1569
JO - Leukemia
JF - Leukemia
IS - 7
ER -