Ontology highlight
ABSTRACT: Background
Relapsed acute lymphoblastic leukemia (ALL) is difficult to treat despite the availability of aggressive therapies. Chimeric antigen receptor-modified T cells targeting CD19 may overcome many limitations of conventional therapies and induce remission in patients with refractory disease.Methods
We infused autologous T cells transduced with a CD19-directed chimeric antigen receptor (CTL019) lentiviral vector in patients with relapsed or refractory ALL at doses of 0.76×10(6) to 20.6×10(6) CTL019 cells per kilogram of body weight. Patients were monitored for a response, toxic effects, and the expansion and persistence of circulating CTL019 T cells.Results
A total of 30 children and adults received CTL019. Complete remission was achieved in 27 patients (90%),
SUBMITTER: Maude SL
PROVIDER: S-EPMC4267531 | biostudies-literature | 2014 Oct
REPOSITORIES: biostudies-literature