Many variables exist in the design of an optimized clinical protocol using autologous CAR-modified tumor-targeted T cells in the treatment of cancer. Patients undergo an initial leukapheresis to isolate autologous T cells. 1. CAR gene transfer of T cells may variably be achieved through retroviral-, lentiviral-, or transposon-mediated technology, with electroporation deemed unsuitable in this current report. 2. Optimal CAR design currently remains unclear although previously published data support a second- or third-generation CAR design over a first-generation CAR. 3. Conditioning therapy appears to favor T-cell persistence and an improved antitumor response. 4. However, the role of postinfusion exogenous cytokine support in obtaining an optimal antitumor response requires additional clinical study. Illustration by Hollie Pegram.

Many variables exist in the design of an optimized clinical protocol using autologous CAR-modified tumor-targeted T cells in the treatment of cancer. Patients undergo an initial leukapheresis to isolate autologous T cells. 1. CAR gene transfer of T cells may variably be achieved through retroviral-, lentiviral-, or transposon-mediated technology, with electroporation deemed unsuitable in this current report. 2. Optimal CAR design currently remains unclear although previously published data support a second- or third-generation CAR design over a first-generation CAR. 3. Conditioning therapy appears to favor T-cell persistence and an improved antitumor response. 4. However, the role of postinfusion exogenous cytokine support in obtaining an optimal antitumor response requires additional clinical study. Illustration by Hollie Pegram.

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