Blood Cancer Journal (Aug 2023)

Metabolic PET/CT analysis of aggressive Non-Hodgkin lymphoma prior to Axicabtagene Ciloleucel CAR-T infusion: predictors of progressive disease, survival, and toxicity

  • William G. Breen,
  • Jason R. Young,
  • Matthew A. Hathcock,
  • Roman O. Kowalchuk,
  • Matthew P. Thorpe,
  • Radhika Bansal,
  • Arushi Khurana,
  • N. Nora Bennani,
  • Jonas Paludo,
  • Jose Villasboas Bisneto,
  • Yucai Wang,
  • Stephen M. Ansell,
  • Jennifer L. Peterson,
  • Patrick B. Johnston,
  • Scott C. Lester,
  • Yi Lin

DOI
https://doi.org/10.1038/s41408-023-00895-7
Journal volume & issue
Vol. 13, no. 1
pp. 1 – 5

Abstract

Read online

Abstract PET/CT is used to evaluate relapsed/refractory non-Hodgkin lymphoma (NHL) prior to chimeric antigen receptor T-cell (CAR-T) infusion at two time points: pre-leukapheresis (pre-leuk) and pre-lymphodepletion chemotherapy (pre-LD). We hypothesized that changes in PET/CT between these time points predict outcomes after CAR-T. Metabolic tumor volume (MTV), total lesion glycolysis (TLG), and other metrics were calculated from pre-leuk and pre-LD PET/CT scans in patients with NHL who received axicabtagene ciloleucel, and assessed for association with outcomes. Sixty-nine patients were analyzed. While single time point PET/CT characteristics were not associated with risk of PD or death, increases from pre-leuk to pre-LD in parenchymal MTV, nodal MTV, TLG of the largest lesion, and total number of lesions were associated with increased risk of death (p < 0.05 for all). LASSO analysis identified increasing extranodal MTV and increasing TLG of the largest lesion as strong predictors of death (AUC 0.74). Greater pre-LD total MTV was associated with higher risk of grade 3+ immune effector cell-associated neurotoxicity syndrome (ICANS) (p = 0.042). Increasing metabolic disease burden during CAR-T manufacturing is associated with increased risk of progression and death. A two variable risk score stratifies prognosis prior to CAR-T infusion and may inform risk-adapted strategies.