Chimeric Antigen Receptor Modified T Cells
Porter D, Kalos M, Frey N, et al




Key Points:
  • Investigators report outcomes and longer follow up from pilot study treating 14 pts with relapsed, refractory CLL with Chimeric Antigen Receptors (CAR)

  • Pts with relapsed or persistent disease and progressed at least within 2 years; received lymphodepleting chemotherapy ending 3-5 days before T cell infusion

  • 6 pts developed fevers within 24 hrs of infusion #1 (3) or #2 (3)

  • CR: 21%; PR: 36%; overall major response rate: 57%

  • All responding pts developed delayed cytokine release syndrome (CRS), with 5 patients requiring intervention

  • Persistence of CTL019 cells detected by flow cytometry in all 6 pts with ongoing responses 5-35 months after infusion

  • All patients had sustained B cell aplasia without any unusual infectious complications.

Implications:

  • CTL019 therapy associated with significant CRS that responds rapidly to anti-cytokine treatment

  • CTL019 cells can induce potent and sustained responses (8/14) for patients with advanced, relapsed and refractory CLL regardless of p53 mutation status.


View the original abstract on the ASH website.






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