Second-Line Tisagenlecleucel or Standard Care in Aggressive B-Cell Lymphoma

Michael R. Bishop(Universitat Autònoma de Barcelona), Michael Dickinson(Universitat Autònoma de Barcelona), Duncan Purtill(Universitat Autònoma de Barcelona), Pere Barba(Universitat Autònoma de Barcelona), Armando Santoro(Universitat Autònoma de Barcelona), Nada Hamad(Universitat Autònoma de Barcelona), Koji Kato(Universitat Autònoma de Barcelona), Anna Sureda(Universitat Autònoma de Barcelona), Richard Greil(Universitat Autònoma de Barcelona), Catherine Thieblemont(Universitat Autònoma de Barcelona), Franck Morschhauser(Universitat Autònoma de Barcelona), Martin Janz(Universitat Autònoma de Barcelona), Ian W. Flinn(Universitat Autònoma de Barcelona), Werner Rabitsch(Universitat Autònoma de Barcelona), Yok‐Lam Kwong(Universitat Autònoma de Barcelona), Marie José Kersten(Universitat Autònoma de Barcelona), Monique C. Minnema(Universitat Autònoma de Barcelona), Harald Holte(Universitat Autònoma de Barcelona), Esther Hian Li Chan(Universitat Autònoma de Barcelona), Joaquín Martínez‐López(Universitat Autònoma de Barcelona), Antonia Müller(Universitat Autònoma de Barcelona), Richard T. Maziarz(Universitat Autònoma de Barcelona), Joseph P. McGuirk(Universitat Autònoma de Barcelona), Emmanuel Bachy(Université Claude Bernard Lyon 1), Steven Le Gouill(Universitat Autònoma de Barcelona), Martin Dreyling(Universitat Autònoma de Barcelona), Hideo Harigae(Universitat Autònoma de Barcelona), David A. Bond(Universitat Autònoma de Barcelona), Charalambos Andreadis(Universitat Autònoma de Barcelona), Peter A. McSweeney(Universitat Autònoma de Barcelona), Mohamed A. Kharfan‐Dabaja(Universitat Autònoma de Barcelona), Simon Newsome(Universitat Autònoma de Barcelona), Evgeny Degtyarev(Universitat Autònoma de Barcelona), Rakesh Awasthi(Universitat Autònoma de Barcelona), Christopher del Corral(Universitat Autònoma de Barcelona), Giovanna Andreola(Universitat Autònoma de Barcelona), Aisha Masood(Universitat Autònoma de Barcelona), Stephen J. Schuster(Universitat Autònoma de Barcelona), Ulrich Jäger(Universitat Autònoma de Barcelona), Peter Borchmann(Universitat Autònoma de Barcelona), Jason R. Westin(Universitat Autònoma de Barcelona)
New England Journal of Medicine
December 14, 2021
Cited by 513Open Access
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Abstract

BACKGROUND: Patient outcomes are poor for aggressive B-cell non-Hodgkin's lymphomas not responding to or progressing within 12 months after first-line therapy. Tisagenlecleucel is an anti-CD19 chimeric antigen receptor T-cell therapy approved for diffuse large B-cell lymphoma after at least two treatment lines. METHODS: We conducted an international phase 3 trial involving patients with aggressive lymphoma that was refractory to or progressing within 12 months after first-line therapy. Patients were randomly assigned to receive tisagenlecleucel with optional bridging therapy (tisagenlecleucel group) or salvage chemotherapy and autologous hematopoietic stem-cell transplantation (HSCT) (standard-care group). The primary end point was event-free survival, defined as the time from randomization to stable or progressive disease at or after the week 12 assessment or death. Crossover to receive tisagenlecleucel was allowed if a defined event occurred at or after the week 12 assessment. Other end points included response and safety. RESULTS: A total of 322 patients underwent randomization. At baseline, the percentage of patients with high-grade lymphomas was higher in the tisagenlecleucel group than in the standard-care group (24.1% vs. 16.9%), as was the percentage with an International Prognostic Index score (range, 0 to 5, with higher scores indicating a worse prognosis) of 2 or higher (65.4% vs. 57.5%). A total of 95.7% of the patients in the tisagenlecleucel group received tisagenlecleucel; 32.5% of the patients in the standard-care group received autologous HSCT. The median time from leukapheresis to tisagenlecleucel infusion was 52 days. A total of 25.9% of the patients in the tisagenlecleucel group had lymphoma progression at week 6, as compared with 13.8% of those in the standard-care group. The median event-free survival in both groups was 3.0 months (hazard ratio for event or death in the tisagenlecleucel group, 1.07; 95% confidence interval, 0.82 to 1.40; P = 0.61). A response occurred in 46.3% of the patients in the tisagenlecleucel group and in 42.5% in the standard-care group. Ten patients in the tisagenlecleucel group and 13 in the standard-care group died from adverse events. CONCLUSIONS: Tisagenlecleucel was not superior to standard salvage therapy in this trial. Additional studies are needed to assess which patients may obtain the most benefit from each approach. (Funded by Novartis; BELINDA ClinicalTrials.gov number, NCT03570892.).


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