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Five-Year Follow-Up Analysis of ZUMA-5: Axicabtagene Ciloleucel in Relapsed/Refractory Indolent Non-Hodgkin Lymphoma

  • Sattva S. Neelapu
  • , Julio C. Chavez
  • , Alison R. Sehgal
  • , Narendranath Epperla
  • , Matthew L. Ulrickson
  • , Emmanuel Bachy
  • , Pashna N. Munshi
  • , Carla Casulo
  • , David G. Maloney
  • , Sven de Vos
  • , Ran Reshef
  • , Lori A. Leslie
  • , Olalekan O. Oluwole
  • , Ibrahim Yakoub-Agha
  • , Rashmi Khanal
  • , Joseph D. Rosenblatt
  • , Jacob Wulff
  • , Rhine R. Shen
  • , Wangshu Zhang
  • , Soumya Poddar
  • Harry Miao, Olga Nikolajeva, Caron A. Jacobson
  • University of Texas MD Anderson Cancer Center
  • Moffitt Cancer Center
  • University of Pittsburgh
  • Ohio State University
  • Banner Health
  • Hospices civils de Lyon
  • University of Pennsylvania
  • University of Rochester
  • Fred Hutchinson Cancer Research Center
  • University of California at Los Angeles
  • Columbia University
  • Vanderbilt University
  • Infinite
  • Fox Chase Cancer Center
  • University of Miami
  • Kite, a Gilead Company
  • Dana-Farber Cancer Institute

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

18 Scopus citations

Abstract

Axicabtagene ciloleucel (axi-cel) is an autologous anti-CD19 chimeric antigen receptor (CAR) T-cell therapy approved for relapsed/refractory (R/R) follicular lymphoma (FL). Here, we report updated clinical outcomes from ZUMA-5 in 159 enrolled patients with R/R indolent non-Hodgkin lymphoma (iNHL; 127 with FL and 31 with marginal zone lymphoma) after a median follow-up of 64.6 months. Patients underwent leukapheresis and received lymphodepleting chemotherapy and axi-cel (2 × 106 CAR T cells/kg). The overall response rate was 90% (75% complete response rate). The median duration of response was 60.4 months, and the median progression-free survival (PFS) was 62.2 months; median time to next treatment and overall survival were not reached (NR). At data cutoff, 55% of patients were alive without requiring subsequent anticancer therapy. Median lymphoma-specific PFS in patients with FL was NR; 34% had progression or death due to lymphoma or study treatment. Notably, after 30 months postinfusion, progression or lymphoma-related deaths were rare. Late-onset toxicities were infrequent and largely unrelated to axi-cel. Durable response and prolonged survival in FL were associated with robust early CAR T-cell expansion and naïve product phenotype. These findings confirm sustained responses and manageable safety with axi-cel in the long term among patients with R/R iNHL and its potential as a curative therapy in FL.

Original languageEnglish
Pages (from-to)3573-3577
Number of pages5
JournalJournal of Clinical Oncology
Volume43
Issue number33
DOIs
StatePublished - Nov 2025

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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