OncoTargets and Therapy · 2019 · 15 citations · 14 references
MedicineHematologyOncologyCancer ImmunologyCell TherapyImmunotherapyCancer ImmunotherapyCell-based ImmunotherapyCellular TherapyChimeric Antigen Receptor T-cell TherapyCytotoxic T Lymphocyte ResponsesAcute Leukemia Cellular TherapyAcute Lymphoblastic Leukemia TherapyAcute Lymphoblastic Leukemia TreatmentRefractory Acute Lymphoblastic LeukemiaRelapsed Acute Lymphoblastic LeukemiaRelapsed Disease TherapyRelapsed LeukemiaT-cell Therapy
BACKGROUND: CD19-modified CAR-T cells greatly influence responses in patients with relapsed/refractory acute lymphoblastic leukemia (ALL). However, recurrence remains a challenge, and reinfusion of CAR-T cells is not always effective. Sequential infusion of humanized CD19-modified and CD22-modified CAR-T cells may overcome this issue and induce remission. METHODS: We examined treatment with sequential infusion of humanized CD19-modified and CD22-modified CAR-T cells in a patient with relapsed ALL previously exposed to murine-derived anti-CD19 CAR-T cells. RESULTS: At ~6 weeks after treatment, repeated bone marrow smear and flow cytometry analysis revealed no lymphoblasts. CONCLUSION: Our results suggest that sequential infusion of humanized CD19-modified and CD22-modified CAR-T cells is a valuable option for relapsed patients with prior infusion of murine-derived, CD19-directed CAR-T cells.
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Chimeric Antigen Receptor T Cells for Sustained Remissions in Leukemia
Shannon L. Maude, Noelle V. Frey, Pamela A. Shaw et al. · New England Journal of Medicine · 2014 · 5.4K citations · Full text
Chimeric Antigen Receptor–Modified T Cells for Acute Lymphoid Leukemia
Stephan A. Grupp, Michael Kalos, David M. Barrett et al. · New England Journal of Medicine · 2013 · 3.5K citations · Full text