Abstract: |
Chimeric antigen receptor (CAR)-modified T cells targeting CD19 expressed by normal and malignant B cells is a unique therapy for patients with chronic lymphocytic leukemia (CLL); recent results highlight the potential of this therapy for patients with relapsed CLL. Because adoptive transfer of CAR-modified T cells is a novel approach, there are issues for the medical oncologist to consider when evaluating current and future clinical trials for CLL patients. This article reviews the impact of CAR design, T-cell production, T-cell dose, conditioning regimens, and tumor burden at the time of CAR-modified T-cell infusion on the efficacy of this therapy. © 2013 Elsevier Inc.. |
Keywords: |
signal transduction; cancer chemotherapy; treatment response; review; nonhuman; clinical trials as topic; drug megadose; outcome assessment; binding affinity; protein domain; antigen expression; lymphocyte proliferation; t-lymphocytes; animals; tumor volume; bendamustine; cyclophosphamide; antineoplastic activity; chimera; minimal residual disease; tumor burden; recombinant proteins; adoptive cell therapy; chimeric antigen receptor; adoptive transfer; gamma irradiation; electroporation; cytokine production; immunophenotyping; drug cytotoxicity; cancer control; cytokine release; leukemia relapse; chronic lymphatic leukemia; immunotherapy, adoptive; t lymphocyte activation; lymphocytopoiesis; cd19 antigen; lymphocyte antigen receptor; antigens, cd19; leukemia, lymphocytic, chronic, b-cell; receptors, antigen; lymphocyte count; pentostatin; leukemia remission; cancer gene therapy; chronic lymphocytic leukemia; cd19; cancer prognosis; cell engineering
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