Survival with Axicabtagene Ciloleucel in Large B-Cell Lymphoma

  • Jason R Westin
  • Olalekan O Oluwole
  • Marie José Kersten
  • David B Miklos
  • Miguel-Angel Perales
  • Armin Ghobadi
  • Aaron P Rapoport
  • Anna Sureda
  • Caron A Jacobson
  • Umar Farooq
  • Tom van Meerten
  • Matthew Ulrickson
  • Mahmoud Elsawy
  • Lori A Leslie
  • Sridhar Chaganti
  • Michael Dickinson
  • Kathleen Dorritie
  • Patrick M Reagan
  • Joseph McGuirk
  • Kevin W Song
  • Peter A Riedell
  • Monique C Minnema
  • Yin Yang
  • Saran Vardhanabhuti
  • Simone Filosto
  • Paul Cheng
  • Shilpa A Shahani
  • Marco Schupp
  • Christina To
  • Frederick L Locke
  • ZUMA-7 Investigators

Abstract

BACKGROUND: In an analysis of the primary outcome of this phase 3 trial, patients with early relapsed or refractory large B-cell lymphoma who received axicabtagene ciloleucel (axi-cel), an autologous anti-CD19 chimeric antigen receptor T-cell therapy, as second-line treatment had significantly longer event-free survival than those who received standard care. Data were needed on longer-term outcomes.

METHODS: In this trial, we randomly assigned patients with early relapsed or refractory large B-cell lymphoma in a 1:1 ratio to receive either axi-cel or standard care (two to three cycles of chemoimmunotherapy followed by high-dose chemotherapy with autologous stem-cell transplantation in patients who had a response). The primary outcome was event-free survival, and key secondary outcomes were response and overall survival. Here, we report the results of the prespecified overall survival analysis at 5 years after the first patient underwent randomization.

RESULTS: A total of 359 patients underwent randomization to receive axi-cel (180 patients) or standard care (179 patients). At a median follow-up of 47.2 months, death had been reported in 82 patients in the axi-cel group and in 95 patients in the standard-care group. The median overall survival was not reached in the axi-cel group and was 31.1 months in the standard-care group; the estimated 4-year overall survival was 54.6% and 46.0%, respectively (hazard ratio for death, 0.73; 95% confidence interval [CI], 0.54 to 0.98; P = 0.03 by stratified two-sided log-rank test). This increased survival with axi-cel was observed in the intention-to-treat population, which included 74% of patients with primary refractory disease and other high-risk features. The median investigator-assessed progression-free survival was 14.7 months in the axi-cel group and 3.7 months in the standard-care group, with estimated 4-year percentages of 41.8% and 24.4%, respectively (hazard ratio, 0.51; 95% CI, 0.38 to 0.67). No new treatment-related deaths had occurred since the primary analysis of event-free survival.

CONCLUSIONS: At a median follow-up of 47.2 months, axi-cel as second-line treatment for patients with early relapsed or refractory large B-cell lymphoma resulted in significantly longer overall survival than standard care. (Funded by Kite; ZUMA-7 ClinicalTrials.gov number, NCT03391466.).

Bibliografische Daten

OriginalspracheEnglisch
ISSN0028-4793
DOIs
StatusVeröffentlicht - 13.07.2023

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Copyright © 2023 Massachusetts Medical Society.

PubMed 37272527