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Axicabtagene Ciloleucel as Second-Line Therapy for Large B-Cell Lymphoma

  • All ZUMA-7 Investigators and Contributing Kite Members
  • Moffitt Cancer Center
  • Stanford University
  • Dana-Farber Cancer Institute
  • Memorial Sloan-Kettering Cancer Center
  • University of Amsterdam
  • Vanderbilt University
  • Washington University St. Louis
  • University of Maryland, Baltimore
  • University of Kansas and University of Kansas Cancer Center
  • Swedish Medical Center
  • Banner Health
  • University of Iowa
  • University of Groningen
  • University of Rochester
  • University of Barcelona
  • Sarah Cannon Research Institute
  • KU Leuven
  • University of British Columbia
  • University of Melbourne
  • Utrecht University
  • The University of Chicago
  • University Hospitals Birmingham NHS Foundation Trust
  • Kite, a Gilead Company
  • Northwestern University
  • University of Texas MD Anderson Cancer Center

Research output: Contribution to journal › Article › peer-review

1490 Scopus citations

Abstract

BACKGROUND: The prognosis of patients with early relapsed or refractory large B-cell lymphoma after the receipt of first-line chemoimmunotherapy is poor. METHODS: In this international, phase 3 trial, we randomly assigned, in a 1:1 ratio, patients with large B-cell lymphoma that was refractory to or had relapsed no more than 12 months after first-line chemoimmunotherapy to receive axicabtagene ciloleucel (axi-cel, an autologous anti-CD19 chimeric antigen receptor T-cell therapy) or standard care (two or three cycles of investigator-selected, protocol-defined chemoimmunotherapy, followed by high-dose chemotherapy with autologous stem-cell transplantation in patients with a response to the chemoimmunotherapy). The primary end point was event-free survival according to blinded central review. Key secondary end points were response and overall survival. Safety was also assessed. RESULTS: A total of 180 patients were randomly assigned to receive axi-cel and 179 to receive standard care. The primary end-point analysis of event-free survival showed that axi-cel therapy was superior to standard care. At a median follow-up of 24.9 months, the median event-free survival was 8.3 months in the axi-cel group and 2.0 months in the standard-care group, and the 24-month event-free survival was 41% and 16%, respectively (hazard ratio for event or death, 0.40; 95% confidence interval, 0.31 to 0.51; P<0.001). A response occurred in 83% of the patients in the axi-cel group and in 50% of those in the standard-care group (with a complete response in 65% and 32%, respectively). In an interim analysis, the estimated overall survival at 2 years was 61% in the axi-cel group and 52% in the standardcare group. Adverse events of grade 3 or higher occurred in 91% of the patients who received axi-cel and in 83% of those who received standard care. Among patients who received axi-cel, grade 3 or higher cytokine release syndrome occurred in 6% and grade 3 or higher neurologic events in 21%. No deaths related to cytokine release syndrome or neurologic events occurred. CONCLUSIONS: Axi-cel therapy led to significant improvements, as compared with standard care, in event-free survival and response, with the expected level of high-grade toxic effects.

Original languageEnglish
Pages (from-to)640-654
Number of pages15
JournalNew England Journal of Medicine
Volume386
Issue number7
DOIs
StatePublished - 17 Feb 2022

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