Abstract |
CD19-targeted chimeric antigen receptor T-cell (CAR-T) therapy has shown promise as treatment of relapsed or refractory B-cell malignancies. However, the clinical utility of early CAR-T monitoring within 1 month after infusion has not been elucidated. In this study, we quantitatively measured CAR-T kinetics in peripheral blood on days 2, 4, 7, 9, 11, 14, 21, and 28 post-infusion using flow cytometry and quantitative polymerase chain reaction in 13 patients with relapsed refractory diffuse large B-cell lymphoma (DLBCL) treated with tisagenlecleucel (tisa-cel). No relationships were identified between bulk CAR-T kinetics and treatment outcomes. Interestingly, the magnitude of CD4+ CAR-T expansion was higher in responders than in nonresponders, while CD8+ CAR-T expansion was minimal in responders. Additionally, CAR-T proliferation was more pronounced in patients with cytokine release syndrome. Our results suggest that CD4+ CAR-T cellular kinetics within 1 month after CAR-T infusion may predict its efficacy after tisa-cel therapy in adult patients with DLBCL.
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Authors | Ryo Hanajiri, Katsuya Furukawa, Marie Nakashima, Yoko Ushijima, Kazuyuki Shimada, Yuichi Ishikawa, Seitaro Terakura, Makoto Murata, Hitoshi Kiyoi |
Journal | [Rinsho ketsueki] The Japanese journal of clinical hematology
(Rinsho Ketsueki)
Vol. 64
Issue 3
Pg. 167-174
( 2023)
ISSN: 0485-1439 [Print] Japan |
PMID | 37019669
(Publication Type: English Abstract, Journal Article)
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Chemical References |
- tisagenlecleucel
- Receptors, Chimeric Antigen
- Receptors, Antigen, T-Cell
- Antigens, CD19
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Topics |
- Adult
- Humans
- Receptors, Chimeric Antigen
(therapeutic use)
- Receptors, Antigen, T-Cell
(therapeutic use)
- Lymphoma, Large B-Cell, Diffuse
(drug therapy)
- T-Lymphocytes
- Immunotherapy, Adoptive
(methods)
- Antigens, CD19
(therapeutic use)
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