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

Research output: Contribution to journalArticlepeer-review

Abstract

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.

Original languageEnglish (US)
Pages (from-to)1564-1569
Number of pages6
JournalLeukemia
Volume38
Issue number7
DOIs
StatePublished - Jul 2024

Bibliographical note

Publisher Copyright:
© The Author(s), under exclusive licence to Springer Nature Limited 2024.

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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