Abstract
Introduction: Axicabtagene ciloleucel is an autologous anti-CD19 chimeric antigen receptor (CAR) T-cell therapy that was recently approved for relapsed or refractory follicular lymphoma following progression on two or more lines of therapy including an anti-CD20 monoclonal antibody with an alkylating agent, providing a therapeutic breakthrough in a subset of indolent non-Hodgkin lymphoma associated with poor clinical outcomes. Areas covered: In this article, we outline the drug profile of axicabtagene ciloleucel in comparison to currently approved agents and other CAR T-cell and T-cell redirecting therapies under investigation for the treatment of relapsed or refractory follicular lymphoma. We also review the efficacy, safety, and pharmacokinetic data from the ZUMA-5 phase II trial, which forms the basis of the recent approval of axicabtagene ciloleucel. Expert opinion: Axicabtagene ciloleucel is the first cellular therapy approved for relapsed or refractory follicular lymphoma, demonstrating high rates of durable responses and a manageable toxicity profile in heavily pre-treated patients.
Original language | English |
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Pages (from-to) | 903-914 |
Number of pages | 12 |
Journal | Expert Review of Anticancer Therapy |
Volume | 22 |
Issue number | 9 |
DOIs | |
State | Published - 2022 |
Keywords
- CAR T-cell
- Follicular lymphoma
- axicabtagene ciloleucel
- bispecific antibody
- cellular therapy
- indolent non-Hodgkin’s lymphoma
- treatment