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CAR T-cell therapy in highly aggressive B-cell lymphoma: emerging biological and clinical insights.
Ali, Alaa; Goy, Andre; Dunleavy, Kieron.
Affiliation
  • Ali A; Stem Cell Transplant and Cellular Immunotherapy Program, Georgetown University, Washington, DC.
  • Goy A; John Theurer Cancer Center at Hackensack University Medical Center, Hackensack, NJ; and.
  • Dunleavy K; Division of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC.
Blood ; 140(13): 1461-1469, 2022 09 29.
Article in En | MEDLINE | ID: mdl-35560330
ABSTRACT
Recently, significant progress has been made in identifying novel therapies, beyond conventional immunochemotherapy strategies, with efficacy in B-cell lymphomas. One such approach involves targeting the CD19 antigen on B cells with autologous-derived chimeric antigen receptor (CAR) cells. This strategy is highly effective in patients with relapsed/refractory diffuse large B-cell lymphoma (DLBCL), as evidenced by recent regulatory approvals. Recent reports suggest that this is an effective strategy for high-grade B-cell lymphoma. The biological underpinnings of these entities and how they overlap with each other and DLBCL continue to be areas of intense investigation. Therefore, as more experience with CAR T-cell approaches is examined, it is interesting to consider how both tumor cell-specific and microenvironmental factors that define these highly aggressive subsets influence susceptibility to this approach.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Lymphoma, Large B-Cell, Diffuse / Receptors, Chimeric Antigen Type of study: Prognostic_studies Limits: Humans Language: En Journal: Blood Year: 2022 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Lymphoma, Large B-Cell, Diffuse / Receptors, Chimeric Antigen Type of study: Prognostic_studies Limits: Humans Language: En Journal: Blood Year: 2022 Type: Article