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- W2305384511 endingPage "617" @default.
- W2305384511 startingPage "608" @default.
- W2305384511 abstract "Abstract The field of cancer immunotherapy has rapidly progressed in the past decade as several therapeutic modalities have entered into the clinic. One such immunotherapy that has shown promise in the treatment of cancer is the use of chimeric antigen receptor (CAR)-modified T lymphocytes. CARs are engineered receptors constructed from antigen recognition regions of antibodies fused to T-cell signaling and costimulatory domains that can be used to reprogram a patient’s T cells to specifically target tumor cells. CAR T-cell therapy has demonstrated sustained complete responses for some patients with advanced leukemia, and a number of CAR therapies are being evaluated in clinical studies. CAR T-cell therapy-associated toxicities, including cytokine release syndrome, macrophage activation syndrome, and tumor lysis syndrome, have been observed and effectively managed in the clinic. In patients with significant clinical responses, sustained B-cell aplasia has also been observed and is a marker of CAR T-cell persistence that might provide long-term disease control. Education on CAR T-cell therapy efficacy and safety management is critical for clinicians and patients who are considering this novel type of treatment. In the present report, the current landscape of CAR T-cell therapy, the effective management of patients undergoing treatment, and which patients are the most suitable candidates for current trials are discussed." @default.
- W2305384511 created "2016-06-24" @default.
- W2305384511 creator A5029763484 @default.
- W2305384511 creator A5029979708 @default.
- W2305384511 date "2016-03-23" @default.
- W2305384511 modified "2023-10-18" @default.
- W2305384511 title "Chimeric Antigen Receptor T-Cell Therapy for the Community Oncologist" @default.
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