Haematologica (Nov 2023)

Effect of delayed cell infusion in patients with large B-cell lymphoma treated with chimeric antigen receptor T-cell therapy

  • Andrew P. Jallouk,
  • Naishu Kui,
  • Ryan Sun,
  • Jason R. Westin,
  • Raphael E. Steiner,
  • Ranjit Nair,
  • Loretta J. Nastoupil,
  • Luis E. Fayad,
  • Ajlan Al Zaki,
  • Misha Hawkins,
  • Sherry Adkins,
  • Mansoor Noorani,
  • Kaberi Das,
  • Jared Henderson,
  • Elizabeth J. Shpall,
  • Partow Kebriaei,
  • Jeremy Ramdial,
  • Christopher R. Flowers,
  • Sattva S. Neelapu,
  • Sairah Ahmed,
  • Paolo Strati

DOI
https://doi.org/10.3324/haematol.2023.284453
Journal volume & issue
Vol. 109, no. 5

Abstract

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Complications occurring after lymphodepleting chemotherapy (LDC) may delay chimeric antigen receptor (CAR) T-cell infusion. The effect of these delays on clinical outcomes is unclear. We performed a retrospective analysis of 240 patients with relapsed/refractory large B-cell lymphoma treated with standard-of-care axicabtagene ciloleucel (axi-cel) and identified 40 patients (16.7%) who had delay in axi-cel infusion. Of these, 85% had delay due to infection. At time of LDC initiation, patients with delayed infusion had lower absolute neutrophil count (P=0.006), lower platelets (P=0.004), lower hemoglobin (P5 days (4.6 vs. 8.2 months; P=0.036), but not 1 day (5.7 vs. 8.2 months; P=0.238). Following propensity score matching, patients with delayed infusion continued to have shorter median PFS (3.5 vs. 6.0 months; P=0.015). Levels of pro-inflammatory cytokines on day of infusion were significantly higher in patients with delayed infusion. Together, these findings suggest that delays in CAR T-cell administration after initiation of LDC are associated with inferior outcomes. Further studies are needed to guide strategies to improve efficacy in such patients.