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Chimeric antigen receptor T-cell therapy

Chimeric antigen receptor T-cell therapies are promising new options for patients with relapsed or refractory diffuse large B-cell lymphoma or acute lymphoblastic leukaemia. They increase complete response rates and the chances of achieving prolonged remission. Chimeric antigen receptor T cells are...

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Detalles Bibliográficos
Autores principales: Burge, Cale, Vanguru, Vinay, Ho, Phoebe Joy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Therapeutic Guidelines 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10664099/
http://dx.doi.org/10.18773/austprescr.2023.003
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author Burge, Cale
Vanguru, Vinay
Ho, Phoebe Joy
author_facet Burge, Cale
Vanguru, Vinay
Ho, Phoebe Joy
author_sort Burge, Cale
collection PubMed
description Chimeric antigen receptor T-cell therapies are promising new options for patients with relapsed or refractory diffuse large B-cell lymphoma or acute lymphoblastic leukaemia. They increase complete response rates and the chances of achieving prolonged remission. Chimeric antigen receptor T cells are specially modified lymphocytes designed to stimulate the body’s own immune system to target malignant cells. The process involves an initial harvest of the patient’s own T cells, genetic modification, T-cell expansion and then reinfusion. Cytokine release syndrome is a major short-term complication of chimeric antigen receptor T-cell therapy. The presentation typically resembles septic shock and can be fatal. Immune effector cell-associated neurotoxicity syndrome is another major short-term complication. It presents with a spectrum of neurological deficits ranging from headache, delirium and anxiety to seizures and coma. There are early promising results with chimeric antigen receptor T-cell therapies in other cancers. These include mantle cell lymphoma, multiple myeloma and some solid organ tumours such as glioblastoma multiforme.
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spelling pubmed-106640992023-12-05 Chimeric antigen receptor T-cell therapy Burge, Cale Vanguru, Vinay Ho, Phoebe Joy Aust Prescr Experimental and Clinical Pharmacology Chimeric antigen receptor T-cell therapies are promising new options for patients with relapsed or refractory diffuse large B-cell lymphoma or acute lymphoblastic leukaemia. They increase complete response rates and the chances of achieving prolonged remission. Chimeric antigen receptor T cells are specially modified lymphocytes designed to stimulate the body’s own immune system to target malignant cells. The process involves an initial harvest of the patient’s own T cells, genetic modification, T-cell expansion and then reinfusion. Cytokine release syndrome is a major short-term complication of chimeric antigen receptor T-cell therapy. The presentation typically resembles septic shock and can be fatal. Immune effector cell-associated neurotoxicity syndrome is another major short-term complication. It presents with a spectrum of neurological deficits ranging from headache, delirium and anxiety to seizures and coma. There are early promising results with chimeric antigen receptor T-cell therapies in other cancers. These include mantle cell lymphoma, multiple myeloma and some solid organ tumours such as glioblastoma multiforme. Therapeutic Guidelines 2023-08-22 2023-08 /pmc/articles/PMC10664099/ http://dx.doi.org/10.18773/austprescr.2023.003 Text en (c) Therapeutic Guidelines https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (CC BY-NC-ND) 4.0 License.
spellingShingle Experimental and Clinical Pharmacology
Burge, Cale
Vanguru, Vinay
Ho, Phoebe Joy
Chimeric antigen receptor T-cell therapy
title Chimeric antigen receptor T-cell therapy
title_full Chimeric antigen receptor T-cell therapy
title_fullStr Chimeric antigen receptor T-cell therapy
title_full_unstemmed Chimeric antigen receptor T-cell therapy
title_short Chimeric antigen receptor T-cell therapy
title_sort chimeric antigen receptor t-cell therapy
topic Experimental and Clinical Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10664099/
http://dx.doi.org/10.18773/austprescr.2023.003
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