Chimeric antigen receptor T-cell (CAR-T) therapy in patients with aggressive B-cell lymphomas. Current outlook after a decade of treatment
Med Clin (Barc). 2022 Apr 8;158(7):327-332.
doi: 10.1016/j.medcli.2021.10.005.
Epub 2021 Dec 3.
[Article in
English,
Spanish]
Affiliations
- 1 Department of Hematology, University Hospital Vall d'Hebron, Barcelona, España.
- 2 Department of Hematology, University Hospital Vall d'Hebron, Barcelona, España; Department of Medicine, Universitat Autònoma de Barcelona, Bellaterra, España; Experimental Hematology, Vall d'Hebron Institute of Oncology (VHIO), Barcelona, España.
- 3 Department of Hematology, University Hospital Vall d'Hebron, Barcelona, España; Department of Medicine, Universitat Autònoma de Barcelona, Bellaterra, España; Experimental Hematology, Vall d'Hebron Institute of Oncology (VHIO), Barcelona, España. Electronic address: pbarba@vhio.net.
Abstract
Chimeric antigen receptor T-cell (CAR-T) therapy has revolutionized the management of patients with diffuse large B-cell lymphoma (DLBCL) who are refractory or relapse after immunochemotherapy. This strategy consists in genetically modifying the patient's own T lymphocytes to favor the recognition of selected tumor antigens. Currently, we have two anti-CD19 CAR-T drugs approved in Spain for patients with DLBCL after two or more prior treatment lines and there are multiple ongoing clinical trials exploring earlier lines of treatment. Both clinical trials and post-marketing real-world data have contributed to better define the efficacy and safety profile of each construct, identifying the main prognostic response factors and improving the management of each step in this therapy. All these aspects are reviewed herein.
Keywords:
Chimeric antigen receptor T-cells; Clinical trial; Diffuse large B-cell lymphoma; Ensayo clínico; Linfocitos T con receptor de antígeno quimérico; Linfoma difuso de células grandes B.
Copyright © 2021 Elsevier España, S.L.U. All rights reserved.
MeSH terms
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Humans
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Immunotherapy, Adoptive / adverse effects
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Lymphoma, Large B-Cell, Diffuse* / drug therapy
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Neoplasm Recurrence, Local / drug therapy
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Receptors, Chimeric Antigen* / therapeutic use
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T-Lymphocytes
Substances
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Receptors, Chimeric Antigen