| Literature DB >> 30031849 |
Sara Ghorashian1, Persis Amrolia2, Paul Veys2.
Abstract
T cells that are genetically modified to express chimeric antigen receptors (CARs) specific for CD19 show great promise for the treatment of relapsed/refractory acute lymphoblastic leukemia (ALL). The first U.S. Food and Drug Administration approval of a cellular cancer therapy in 2017, Novartis's CD19-targeting CAR T-cell product Kymriah™ within the context of relapsed/refractory pediatric ALL, followed rapidly by approval of Kite's Yescarta™ and, more recently, Kymriah™ for diffuse large B-cell indications in adults, highlights the pace of progress made in this field. In this review, we will consider the latest evidence from CAR T-cell therapy for B-lineage ALL. We discuss the barriers to CAR T-cell therapy for ALL patients and give a perspective on the strategy we have taken to date to widen access to CAR T-cell therapy for UK pediatric patients with high-risk ALL.Entities:
Mesh:
Substances:
Year: 2018 PMID: 30031849 DOI: 10.1016/j.exphem.2018.07.002
Source DB: PubMed Journal: Exp Hematol ISSN: 0301-472X Impact factor: 3.084