Chimeric antigen receptor T-cell therapy Journal Article


Authors: Ogba, N.; Arwood, N. M.; Bartlett, N. L.; Bloom, M.; Brown, P.; Brown, C.; Budde, E. L.; Carlson, R.; Farnia, S.; Fry, T. J.; Garber, M.; Gardner, R. A.; Gurschick, L.; Kropf, P.; Reitan, J. J.; Sauter, C.; Shah, B.; Shpall, E. J.; Rosen, S. T.
Article Title: Chimeric antigen receptor T-cell therapy
Abstract: Patients with relapsed or refractory (R/R) cancers have a poor prognosis and limited treatment options. The recent approval of 2 chimeric antigen receptor (CAR) autologous T-cell products for R/R B-cell acute lymphoblastic leukemia and non-Hodgkin’s lymphoma treatment is setting the stage for what is possible in other diseases. However, there are important factors that must be considered, including patient selection, toxicity management, and costs associated with CAR T-cell therapy. To begin to address these issues, NCCN organized a task force consisting of a multidisciplinary panel of experts in oncology, cancer center administration, and health policy, which met for the first time in March 2018. This report describes the current state of CAR T-cell therapy and future strategies that should be considered as the application of this novel immunotherapy expands and evolves. © JNCCN—Journal of the National Comprehensive Cancer Network.
Journal Title: Journal of the National Comprehensive Cancer Network
Volume: 16
Issue: 9
ISSN: 1540-1405
Publisher: Harborside Press  
Date Published: 2018-09-01
Start Page: 1093
End Page: 1106
Language: English
DOI: 10.6004/jnccn.2018.0073
PROVIDER: scopus
PUBMED: 30181421
DOI/URL:
Notes: Article -- Export Date: 1 October 2018 -- Source: Scopus
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  1. Craig Steven Sauter
    334 Sauter