The discovery and development of tisagenlecleucel for the treatment of adult patients with relapsed or refractory follicular lymphoma
| dc.contributor.author | Kungwankiattichai S. | |
| dc.contributor.author | Maziarz R.T. | |
| dc.contributor.correspondence | Kungwankiattichai S. | |
| dc.contributor.other | Mahidol University | |
| dc.date.accessioned | 2025-10-16T18:12:32Z | |
| dc.date.available | 2025-10-16T18:12:32Z | |
| dc.date.issued | 2025-01-01 | |
| dc.description.abstract | Introduction: Follicular lymphoma (FL) is an indolent yet incurable subtype of non-Hodgkin lymphoma characterized by repeated relapses and diminishing responses with each treatment line. Although front-line chemoimmunotherapy achieves high initial response rates, a subset of patients–particularly those with early relapse (POD24)–experience poor outcomes and require alternative therapies. Tisagenlecleucel (tisa-cel), a CD19-directed chimeric antigen receptor (CAR) T-cell therapy, has emerged as a promising option for relapsed or refractory (r/r) FL, offering the potential for deep and durable remissions. Areas covered: This review covers the scientific rationale, preclinical innovations, and clinical development of tisa-cel, from its origins in 2<sup>nd</sup>-generation CAR-T engineering to its pivotal trials in hematologic malignancies. It is based on a literature search using PubMed, Embase, and conference abstracts from major hematology meetings from 1987 to April 2025. The paper deta ils the ELARA trial outcomes, subsequent long-term and real-world data, and the competitive landscape of third-line therapies for r/r FL. Expert opinion: Tisa-cel has demonstrated high response rates and sustained remissions with a favorable safety profile in heavily pretreated FL, including high-risk populations such as those with POD24. While bispecific antibodies offer convenient outpatient administration, CAR-T cell therapy provides the potential for deep and durable remissions. The 4-1BB costimulatory domain used in tisa-cel and liso-cel is associated with a lower incidence of severe CRS and ICANS compared to CD28-based constructs. the field evolves, careful patient selection and head-to-head trials will be essential to refine therapeutic sequencing in r/r FL. | |
| dc.identifier.citation | Expert Opinion on Drug Discovery (2025) | |
| dc.identifier.doi | 10.1080/17460441.2025.2567291 | |
| dc.identifier.eissn | 1746045X | |
| dc.identifier.issn | 17460441 | |
| dc.identifier.pmid | 41039722 | |
| dc.identifier.scopus | 2-s2.0-105018188904 | |
| dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/123456789/112601 | |
| dc.rights.holder | SCOPUS | |
| dc.subject | Pharmacology, Toxicology and Pharmaceutics | |
| dc.title | The discovery and development of tisagenlecleucel for the treatment of adult patients with relapsed or refractory follicular lymphoma | |
| dc.type | Article | |
| mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=105018188904&origin=inward | |
| oaire.citation.title | Expert Opinion on Drug Discovery | |
| oairecerif.author.affiliation | Oregon Health & Science University | |
| oairecerif.author.affiliation | Siriraj Hospital |
