Lisocabtagene maraleucel in follicular lymphoma: The phase 2 TRANSCEND FL study Journal Article


Authors: Morschhauser, F.; Dahiya, S.; Palomba, M. L.; Garcia-Sancho, A. M.; Reguera Ortega, J. L.; Kuruvilla, J.; Jäger, U.; Cartron, G.; Izutsu, K.; Dreyling, M.; Kahl, B.; Ghesquieres, H.; Ardeshna, K.; Goto, H.; Barbui, A. M.; Abramson, J. S.; Borchmann, P.; Fleury, I.; Mielke, S.; Skarbnik, A.; de Vos, S.; Kamdar, M.; Karmali, R.; Viardot, A.; Farazi, T.; Fasan, O.; Lymp, J.; Vedal, M.; Nishii, R.; Avilion, A.; Papuga, J.; Kumar, J.; Nastoupil, L. J.
Article Title: Lisocabtagene maraleucel in follicular lymphoma: The phase 2 TRANSCEND FL study
Abstract: An unmet need exists for patients with relapsed/refractory (R/R) follicular lymphoma (FL) and high-risk disease features, such as progression of disease within 24 months (POD24) from first-line immunochemotherapy or disease refractory to both CD20-targeting agent and alkylator (double refractory), due to no established standard of care and poor outcomes. Chimeric antigen receptor (CAR) T cell therapy is an option in R/R FL after two or more lines of prior systemic therapy, but there is no consensus on its optimal timing in the disease course of FL, and there are no data in second-line (2L) treatment of patients with high-risk features. Lisocabtagene maraleucel (liso-cel) is an autologous, CD19-directed, 4-1BB CAR T cell product. The phase 2 TRANSCEND FL study evaluated liso-cel in patients with R/R FL, including 2L patients who all had POD24 from diagnosis after treatment with anti-CD20 antibody and alkylator <= 6 months of FL diagnosis and/or met modified Groupe d'Etude des Lymphomes Folliculaires criteria. Primary/key secondary endpoints were independent review committee-assessed overall response rate (ORR)/complete response (CR) rate. At data cutoff, 130 patients had received liso-cel (median follow-up, 18.9 months). Primary/key secondary endpoints were met. In third-line or later FL (n = 101), ORR was 97% (95% confidence interval (CI): 91.6-99.4), and CR rate was 94% (95% CI: 87.5-97.8). In 2L FL (n = 23), ORR was 96% (95% CI: 78.1-99.9); all responders achieved CR. Cytokine release syndrome occurred in 58% of patients (grade >= 3, 1%); neurological events occurred in 15% of patients (grade >= 3, 2%). Liso-cel demonstrated efficacy and safety in patients with R/R FL, including high-risk 2L FL. ClinicalTrials.gov identifier: NCT04245839. Results of the phase 2 trial of CD19 CAR T cell therapy lisocabtagene maraleucel in patients with relapsed or refractory follicular lymphoma, most of whom were treated in a third-line or later setting, show encouraging objective response rates in these high-risk patients.
Keywords: diagnosis; guidelines; outcomes; therapy; non-hodgkin-lymphoma; treatment patterns
Journal Title: Nature Medicine
Volume: 30
Issue: 8
ISSN: 1078-8956
Publisher: Nature Publishing Group  
Date Published: 2024-08-01
Start Page: 2199
End Page: 2207
Language: English
ACCESSION: WOS:001238211500001
DOI: 10.1038/s41591-024-02986-9
PROVIDER: wos
PMCID: PMC11333271
PUBMED: 38830991
Notes: Source: Wos
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  1. Maria Lia Palomba
    416 Palomba