TY - JOUR
T1 - Point-of-care anti-CD19 chimeric antigen receptor T-cell therapy for relapsed/refractory follicular lymphoma
AU - Fried, Shalev
AU - Shkury, Eden
AU - Itzhaki, Orit
AU - Sdayoor, Inbal
AU - Yerushalmi, Ronit
AU - Shem-Tov, Noga
AU - Danylesko, Ivetta
AU - Jacoby, Elad
AU - Shouval, Roni
AU - Kedmi, Meirav
AU - Marcus, Ronit
AU - Nagler, Arnon
AU - Shimoni, Avichai
AU - Avigdor, Abraham
N1 - Publisher Copyright:
© 2023 Informa UK Limited, trading as Taylor & Francis Group.
PY - 2023
Y1 - 2023
N2 - Patients with relapsed/refractory follicular lymphoma (R/R-FL) often require multiple treatment lines. We performed a phase 1b/2 single-center clinical trial of autologous point-of-care anti-CD19 chimeric antigen receptor (CAR) T-cells in R/R-FL patients treated patients with ≥ 2 treatment lines. All 26 patients enrolled received CAR T-cell infusion at a median of 11 days after leukapheresis. Seventy-seven percent of patients had POD24. At enrollment, disease stage was III-IV in 85% of the patients, 77% had high-risk FLIPI score, and 77% had progressive disease. Grade III-IV cytokine release and immune effector cell-associated neurotoxicity syndromes occurred in 12% and 16% of the patients, respectively. Overall response rate at 1-month was 88%. The median follow-up was 15.4 months. One-year overall and progression-free survival were 100% and 63%, respectively. In conclusion, point-of-care CAR T-cell, manufactured within 11 days, induced a high response rate with an acceptable safety profile in patients with high-risk R/R-FL.
AB - Patients with relapsed/refractory follicular lymphoma (R/R-FL) often require multiple treatment lines. We performed a phase 1b/2 single-center clinical trial of autologous point-of-care anti-CD19 chimeric antigen receptor (CAR) T-cells in R/R-FL patients treated patients with ≥ 2 treatment lines. All 26 patients enrolled received CAR T-cell infusion at a median of 11 days after leukapheresis. Seventy-seven percent of patients had POD24. At enrollment, disease stage was III-IV in 85% of the patients, 77% had high-risk FLIPI score, and 77% had progressive disease. Grade III-IV cytokine release and immune effector cell-associated neurotoxicity syndromes occurred in 12% and 16% of the patients, respectively. Overall response rate at 1-month was 88%. The median follow-up was 15.4 months. One-year overall and progression-free survival were 100% and 63%, respectively. In conclusion, point-of-care CAR T-cell, manufactured within 11 days, induced a high response rate with an acceptable safety profile in patients with high-risk R/R-FL.
KW - Chimeric antigen receptor
KW - follicular lymphoma
KW - point-of-care
UR - http://www.scopus.com/inward/record.url?scp=85167796148&partnerID=8YFLogxK
U2 - 10.1080/10428194.2023.2246611
DO - 10.1080/10428194.2023.2246611
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C2 - 37565578
AN - SCOPUS:85167796148
SN - 1042-8194
VL - 64
SP - 1956
EP - 1963
JO - Leukemia and Lymphoma
JF - Leukemia and Lymphoma
IS - 12
ER -