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Chimeric antigen receptor T-cell infusion for large B-cell lymphoma in complete remission: a center for international blood and marrow transplant research analysis

  • Trent P. Wang,
  • Kwang W. Ahn,
  • Mazyar Shadman,
  • Manmeet Kaur,
  • Nausheen Ahmed,
  • Ulrike Bacher,
  • Jan Cerny,
  • Andy Chen,
  • Narendranath Epperla,
  • Matthew Frigault,
  • Natalie Grover,
  • Bradley Haverkos,
  • Brian Hill,
  • Nasheed Hossain,
  • Madiha Iqbal,
  • Tania Jain,
  • Maxwell M. Krem,
  • Joseph Maakaron,
  • Dipenkumar Modi,
  • Muhamad Alhaj Moustafa,
  • Peter Riedell,
  • Bipin Savani,
  • R. Alejandro Sica,
  • Anna Sureda,
  • Kitsada Wudhikarn,
  • Alex F. Herrera,
  • Craig Sauter,
  • Mehdi Hamadani,
  • Antonio Jimenez Jimenez

摘要

CD19 CAR T-cell (CAR-T) therapy is commonly administered to patients with relapsed or refractory large B-cell lymphomas (LBCL), but salvage or bridging therapy can sometimes lead to a complete response (CR) prior to infusion. Limited studies have assessed the outcomes of patients infused in CR. A total of 134 patients with LBCL in CR prior to CAR-T infusion were identified from the CIBMTR registry, with median prior lines of therapy of 3 (range 2–9). At two years post-infusion, the probability of progression-free survival was 43.5% (95% CI 34.4–52.8) and the probability of overall survival was 63.8% (95% CI 54.4–72.6). The cumulative incidence rates of non-relapse mortality and relapse/progression at two years were 9.2% (95% CI 4.5–15.4) and 47.3% (95% CI 38.2–56.6), respectively. The rate of grade 3 or higher cytokine release syndrome (CRS) and immune effector cell-associated neurotoxicity syndrome (ICANS) were 2.2% and 8.2%, respectively. In summary, CAR-T in heavily pretreated patients with LBCL who are in CR following two or more lines of prior therapy demonstrate that a subset of patients may remain free of progression at two years. Additionally, the toxicity profile was impressive with very low rates of grade 3 CRS and ICANS.