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Chimeric antigen receptor T-cell therapy in acute myeloid leukemia

Treatment outcome of relapsed or refractory AML patients remains dismal and new treatment options are needed. Adoptive cell therapy using CAR-T cells is a potentially interesting approach in this. RECENT FINDINGS: Several potentially interesting AML targets are being investigated with CAR-T therapy...

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Autores principales: Koedam, Jan, Wermke, Martin, Ehninger, Armin, Cartellieri, Marc, Ehninger, Gerhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8815830/
https://www.ncbi.nlm.nih.gov/pubmed/35013048
http://dx.doi.org/10.1097/MOH.0000000000000703
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author Koedam, Jan
Wermke, Martin
Ehninger, Armin
Cartellieri, Marc
Ehninger, Gerhard
author_facet Koedam, Jan
Wermke, Martin
Ehninger, Armin
Cartellieri, Marc
Ehninger, Gerhard
author_sort Koedam, Jan
collection PubMed
description Treatment outcome of relapsed or refractory AML patients remains dismal and new treatment options are needed. Adoptive cell therapy using CAR-T cells is a potentially interesting approach in this. RECENT FINDINGS: Several potentially interesting AML targets are being investigated with CAR-T therapy with over 60 clinical trials listed on clinicaltrials.gov. The first clinical data are only just emerging with mixed results, once more proving that further research is needed. SUMMARY: Adoptive cell therapy using chimeric antigen receptor T cells is being investigated in AML through many clinical trials. So far, no AML-specific antigen has been identified, requiring additional strategies to mitigate on-target off-tumor toxicity and to increase efficacy. Focus point is to acquire control over the CAR T cells once administered. Strategies to do so include biodegradable CARs, inducible CARs, suicide-switch containing CARs and two-component modular CARs. Limited and mixed results are available, confirming the risk of lasting toxicity for nonswitchable CARs. Initial results of modular CARs suggest toxicity can be mitigated whilst maintaining CAR activity by the use of modular CAR concepts that allows for ‘ON’ and ‘OFF’ switching.
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spelling pubmed-88158302022-02-09 Chimeric antigen receptor T-cell therapy in acute myeloid leukemia Koedam, Jan Wermke, Martin Ehninger, Armin Cartellieri, Marc Ehninger, Gerhard Curr Opin Hematol MYELOID DISEASE: Edited by Stephanie Halene Treatment outcome of relapsed or refractory AML patients remains dismal and new treatment options are needed. Adoptive cell therapy using CAR-T cells is a potentially interesting approach in this. RECENT FINDINGS: Several potentially interesting AML targets are being investigated with CAR-T therapy with over 60 clinical trials listed on clinicaltrials.gov. The first clinical data are only just emerging with mixed results, once more proving that further research is needed. SUMMARY: Adoptive cell therapy using chimeric antigen receptor T cells is being investigated in AML through many clinical trials. So far, no AML-specific antigen has been identified, requiring additional strategies to mitigate on-target off-tumor toxicity and to increase efficacy. Focus point is to acquire control over the CAR T cells once administered. Strategies to do so include biodegradable CARs, inducible CARs, suicide-switch containing CARs and two-component modular CARs. Limited and mixed results are available, confirming the risk of lasting toxicity for nonswitchable CARs. Initial results of modular CARs suggest toxicity can be mitigated whilst maintaining CAR activity by the use of modular CAR concepts that allows for ‘ON’ and ‘OFF’ switching. Lippincott Williams & Wilkins 2022-03 2022-01-10 /pmc/articles/PMC8815830/ /pubmed/35013048 http://dx.doi.org/10.1097/MOH.0000000000000703 Text en Copyright © 2022 The Author(s). Published by Wolters Kluwer Health, Inc. 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 License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle MYELOID DISEASE: Edited by Stephanie Halene
Koedam, Jan
Wermke, Martin
Ehninger, Armin
Cartellieri, Marc
Ehninger, Gerhard
Chimeric antigen receptor T-cell therapy in acute myeloid leukemia
title Chimeric antigen receptor T-cell therapy in acute myeloid leukemia
title_full Chimeric antigen receptor T-cell therapy in acute myeloid leukemia
title_fullStr Chimeric antigen receptor T-cell therapy in acute myeloid leukemia
title_full_unstemmed Chimeric antigen receptor T-cell therapy in acute myeloid leukemia
title_short Chimeric antigen receptor T-cell therapy in acute myeloid leukemia
title_sort chimeric antigen receptor t-cell therapy in acute myeloid leukemia
topic MYELOID DISEASE: Edited by Stephanie Halene
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8815830/
https://www.ncbi.nlm.nih.gov/pubmed/35013048
http://dx.doi.org/10.1097/MOH.0000000000000703
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