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Third-generation anti-CD19 CAR T cells for relapsed/refractory chronic lymphocytic leukemia: a phase 1/2 study

Authors

  • P. Derigs
  • M.L. Schubert
  • P. Dreger
  • A. Schmitt
  • S. Yousefian
  • S. Haas
  • C. Röthemeier
  • B. Neuber
  • A. Hückelhoven-Krauss
  • M. Brüggemann
  • H. Bernhard
  • G. Kobbe
  • A. Lindemann
  • M. Rummel
  • B. Michels
  • F. Korell
  • A.D. Ho
  • C. Müller-Tidow
  • M. Schmitt

Journal

  • Leukemia

Citation

  • Leukemia 38 (11): 2419-2428

Abstract

  • Third-generation chimeric antigen receptor T cells (CARTs) for relapsed or refractory (r/r) chronic lymphocytic leukemia (CLL) may improve efficacy compared to second-generation CARTs due to their enhanced CAR design. We performed the first phase 1/2 investigator-initiated trial evaluating escalating doses of third-generation CARTs (HD-CAR-1) targeting CD19 in patients with r/r CLL and B-cell lymphoma. CLL eligibility criteria were failure to two therapy lines including at least one pathway inhibitor and/or allogeneic hematopoietic cell transplantation. Nine heavily pretreated patients received HD-CAR-1 at dose levels ranging from 1 × 10(6) to 200 × 10(6) CART/m(2). In-house HD-CAR-1 manufacturing was successful for all patients. While neurotoxicity was absent, one case of grade 3 cytokine release syndrome was observed. By day 90, six patients (67%) attained a CR, five of these (83%) with undetectable MRD. With a median follow-up of 27 months, 2-year PFS and OS were 30% and 69%, respectively. HD-CAR-1 products of responders contained significantly more CD4 + T cells compared to non-responders. In non-responders, a strong enrichment of effector memory-like CD8 + T cells with high expression of CD39 and/or CD197 was observed. HD-CAR-1 demonstrated encouraging efficacy and exceptionally low treatment-specific toxicity, presenting new treatment options for patients with r/r CLL.


DOI

doi:10.1038/s41375-024-02392-7