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Long-term outcomes of patients with large B-cell lymphoma treated with axicabtagene ciloleucel and prophylactic corticosteroids

  • Olalekan O. Oluwole,
  • Edouard Forcade,
  • Javier Muñoz,
  • Sophie de Guibert,
  • Julie M. Vose,
  • Nancy L. Bartlett,
  • Yi Lin,
  • Abhinav Deol,
  • Peter McSweeney,
  • Andre H. Goy,
  • Marie José Kersten,
  • Caron A. Jacobson,
  • Umar Farooq,
  • Monique C. Minnema,
  • Catherine Thieblemont,
  • John M. Timmerman,
  • Patrick Stiff,
  • Irit Avivi,
  • Dimitrios Tzachanis,
  • Yan Zheng,
  • Saran Vardhanabhuti,
  • Jenny Nater,
  • Rhine R. Shen,
  • Harry Miao,
  • Jenny J. Kim,
  • Tom van Meerten

摘要

ZUMA-1 safety management cohort 6 investigated the impact of prophylactic corticosteroids and earlier corticosteroids and/or tocilizumab on the incidence and severity of cytokine release syndrome (CRS) and neurologic events (NEs) following axicabtagene ciloleucel (axi-cel) in patients with relapsed/refractory large B-cell lymphoma (R/R LBCL). Prior analyses of cohort 6 with limited follow-up demonstrated no Grade ≥3 CRS, a low rate of NEs, and high response rates, without negatively impacting axi-cel pharmacokinetics. Herein, long-term outcomes of cohort 6 (N = 40) are reported (median follow-up, 26.9 months). Since the 1-year analysis (Oluwole, et al. Blood. 2022;138[suppl 1]:2832), no new CRS was reported. Two new NEs occurred in two patients (Grade 2 dementia unrelated to axi-cel; Grade 5 axi-cel–related leukoencephalopathy). Six new infections and eight deaths (five progressive disease; one leukoencephalopathy; two COVID-19) occurred. Objective and complete response rates remained at 95% and 80%, respectively. Median duration of response and progression-free survival were reached at 25.9 and 26.8 months, respectively. Median overall survival has not yet been reached. Eighteen patients (45%) remained in ongoing response at data cutoff. With ≥2 years of follow-up, prophylactic corticosteroids and earlier corticosteroids and/or tocilizumab continued to demonstrate CRS improvement without compromising efficacy outcomes, which remained high and durable.