| Literature DB >> 31780119 |
Veronika Bachanova1, Miguel-Angel Perales2, Jeremy S Abramson3.
Abstract
Approximately 65% of patients with diffuse large B-cell lymphoma are cured with first-line therapy. However, approximately 10% to 15% exhibit primary refractory disease, and 20% to 25% experience relapse after initial response. Eligible patients receive second-line therapy followed by high-dose chemotherapy and an autologous hematopoietic stem cell transplant, previously the only potentially curative option for this population. Recently approved chimeric antigen receptor (CAR) T-cell therapies offer an alternative curative option for patients who have experienced a second-line or later relapse or whose disease is refractory. CD19-targeting CAR T cells are autologous T cells expressing an anti-CD19 CAR that, when reintroduced to the patient, identify and kill CD19+ B cells. Because of the novelty of CAR T-cell therapy and the complexity of this patient population, identification of ideal candidates is still being defined. This article summarizes 3 patient cases, focusing on the important aspects of patient selection for CAR T-cell therapy.Entities:
Keywords: CAR T-cell therapy; Chimeric antigen receptor; Diffuse large B-cell lymphoma
Year: 2019 PMID: 31780119 DOI: 10.1016/j.blre.2019.100640
Source DB: PubMed Journal: Blood Rev ISSN: 0268-960X Impact factor: 8.250