Tisagenlecleucel in Adult Relapsed or Refractory Diffuse Large B-Cell Lymphoma

Stephen J. Schuster(Peter MacCallum Cancer Centre), Michael Bishop(Peter MacCallum Cancer Centre), Constantine S. Tam(The University of Melbourne), Edmund K. Waller(Emory University), Peter Borchmann(Peter MacCallum Cancer Centre), Joseph P. McGuirk(Peter MacCallum Cancer Centre), Ulrich Jäger(Peter MacCallum Cancer Centre), Samantha Jaglowski(The Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute), Charalambos Andreadis(University of California, San Francisco), Jason R. Westin(The University of Texas MD Anderson Cancer Center), Isabelle Fleury(Peter MacCallum Cancer Centre), Veronika Bachanová(University of Minnesota), S.R. Foley(Peter MacCallum Cancer Centre), P. Joy Ho(The University of Sydney), Stephan Mielke(Peter MacCallum Cancer Centre), John Magenau(University of Michigan), Harald Holte(Oslo University Hospital), Serafino Pantano(Novartis (Switzerland)), Lida Pacaud(Peter MacCallum Cancer Centre), Rakesh Awasthi(Novartis (Switzerland)), Jufen Chu(Peter MacCallum Cancer Centre), Özlem Anak(Peter MacCallum Cancer Centre), Gilles Salles(Université Claude Bernard Lyon 1), Richard T. Maziarz(Oregon Health & Science University)
New England Journal of Medicine
December 1, 2018
Cited by 4,007Open Access
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Abstract

BACKGROUND: Patients with diffuse large B-cell lymphoma that is refractory to primary and second-line therapies or that has relapsed after stem-cell transplantation have a poor prognosis. The chimeric antigen receptor (CAR) T-cell therapy tisagenlecleucel targets and eliminates CD19-expressing B cells and showed efficacy against B-cell lymphomas in a single-center, phase 2a study. METHODS: We conducted an international, phase 2, pivotal study of centrally manufactured tisagenlecleucel involving adult patients with relapsed or refractory diffuse large B-cell lymphoma who were ineligible for or had disease progression after autologous hematopoietic stem-cell transplantation. The primary end point was the best overall response rate (i.e., the percentage of patients who had a complete or partial response), as judged by an independent review committee. RESULTS: A total of 93 patients received an infusion and were included in the evaluation of efficacy. The median time from infusion to data cutoff was 14 months (range, 0.1 to 26). The best overall response rate was 52% (95% confidence interval, 41 to 62); 40% of the patients had complete responses, and 12% had partial responses. Response rates were consistent across prognostic subgroups. At 12 months after the initial response, the rate of relapse-free survival was estimated to be 65% (79% among patients with a complete response). The most common grade 3 or 4 adverse events of special interest included cytokine release syndrome (22%), neurologic events (12%), cytopenias lasting more than 28 days (32%), infections (20%), and febrile neutropenia (14%). Three patients died from disease progression within 30 days after infusion. No deaths were attributed to tisagenlecleucel, cytokine release syndrome, or cerebral edema. No differences between response groups in tumor expression of CD19 or immune checkpoint-related proteins were found. CONCLUSIONS: In this international study of CAR T-cell therapy in relapsed or refractory diffuse large B-cell lymphoma in adults, high rates of durable responses were produced with the use of tisagenlecleucel. (Funded by Novartis; JULIET ClinicalTrials.gov number, NCT02445248 .).


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