Chimeric Antigen Receptor T Cells for Sustained Remissions in Leukemia
University of Pennsylvania · Children's Hospital of Philadelphia
Abstract
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.
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.
Citation impact
- FWCI
- 180.64
- Percentile
- 100%
- References
- 31
Authors
19- SLShannon L. MaudeCorresponding
University of Pennsylvania, Children's Hospital of Philadelphia
- NVNoelle V. Frey
University of Pennsylvania
- PAPamela A. Shaw
University of Pennsylvania
- RARichard Aplenc
Children's Hospital of Philadelphia, University of Pennsylvania
- DMDavid M. Barrett
University of Pennsylvania, Children's Hospital of Philadelphia
Topics & keywords
- Chimeric antigen receptor
- Immunology
- Internal medicine
- Cytokine release syndrome
- Medicine
- Transplantation
- Oncology
- Immunotherapy
- Good health and well-being