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Novel agents and regimens in acute myeloid leukemia: latest updates from 2022 ASH Annual Meeting
Developments in investigational agents and novel regimens in acute myeloid leukemia (AML) were reported in the 2022 American Society of Hematology (ASH) annual meeting. Encouraging efficacy data were presented from first-in-human studies of two investigational menin inhibitors, SNDX-5613 and KO-539,...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9983204/ https://www.ncbi.nlm.nih.gov/pubmed/36869366 http://dx.doi.org/10.1186/s13045-023-01411-x |
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author | DiNardo, Katherine W. LeBlanc, Thomas W. Chen, Hui |
author_facet | DiNardo, Katherine W. LeBlanc, Thomas W. Chen, Hui |
author_sort | DiNardo, Katherine W. |
collection | PubMed |
description | Developments in investigational agents and novel regimens in acute myeloid leukemia (AML) were reported in the 2022 American Society of Hematology (ASH) annual meeting. Encouraging efficacy data were presented from first-in-human studies of two investigational menin inhibitors, SNDX-5613 and KO-539, in relapsed and refractory (R/R) acute myeloid leukemia (AML) with KMT2A rearrangement or mutant NPM1, with overall response rates (ORR) of 53% (32/60) and 40% (8/20), respectively. The addition of the novel drug pivekimab sunirine, a first-in-class antibody–drug conjugate targeting CD123, to azacitidine and venetoclax in R/R AML resulted in an ORR of 45% (41/91), which rose to 53% in those who were venetoclax naïve. Additional novel triplet treatment combinations included the addition of magrolimab, an anti-CD47 antibody, to azacitidine and venetoclax, with an ORR of 81% (35/43) in newly diagnosed AML, including an ORR of 74% (20/27) in TP53 mutated AML. The addition of the FLT3 inhibitor gilteritinib to azacitidine/venetoclax was also featured, with an ORR of 100% (27/27) in newly diagnosed AML and an ORR of 70% (14/20) in R/R AML. |
format | Online Article Text |
id | pubmed-9983204 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-99832042023-03-04 Novel agents and regimens in acute myeloid leukemia: latest updates from 2022 ASH Annual Meeting DiNardo, Katherine W. LeBlanc, Thomas W. Chen, Hui J Hematol Oncol Correspondence Developments in investigational agents and novel regimens in acute myeloid leukemia (AML) were reported in the 2022 American Society of Hematology (ASH) annual meeting. Encouraging efficacy data were presented from first-in-human studies of two investigational menin inhibitors, SNDX-5613 and KO-539, in relapsed and refractory (R/R) acute myeloid leukemia (AML) with KMT2A rearrangement or mutant NPM1, with overall response rates (ORR) of 53% (32/60) and 40% (8/20), respectively. The addition of the novel drug pivekimab sunirine, a first-in-class antibody–drug conjugate targeting CD123, to azacitidine and venetoclax in R/R AML resulted in an ORR of 45% (41/91), which rose to 53% in those who were venetoclax naïve. Additional novel triplet treatment combinations included the addition of magrolimab, an anti-CD47 antibody, to azacitidine and venetoclax, with an ORR of 81% (35/43) in newly diagnosed AML, including an ORR of 74% (20/27) in TP53 mutated AML. The addition of the FLT3 inhibitor gilteritinib to azacitidine/venetoclax was also featured, with an ORR of 100% (27/27) in newly diagnosed AML and an ORR of 70% (14/20) in R/R AML. BioMed Central 2023-03-03 /pmc/articles/PMC9983204/ /pubmed/36869366 http://dx.doi.org/10.1186/s13045-023-01411-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Correspondence DiNardo, Katherine W. LeBlanc, Thomas W. Chen, Hui Novel agents and regimens in acute myeloid leukemia: latest updates from 2022 ASH Annual Meeting |
title | Novel agents and regimens in acute myeloid leukemia: latest updates from 2022 ASH Annual Meeting |
title_full | Novel agents and regimens in acute myeloid leukemia: latest updates from 2022 ASH Annual Meeting |
title_fullStr | Novel agents and regimens in acute myeloid leukemia: latest updates from 2022 ASH Annual Meeting |
title_full_unstemmed | Novel agents and regimens in acute myeloid leukemia: latest updates from 2022 ASH Annual Meeting |
title_short | Novel agents and regimens in acute myeloid leukemia: latest updates from 2022 ASH Annual Meeting |
title_sort | novel agents and regimens in acute myeloid leukemia: latest updates from 2022 ash annual meeting |
topic | Correspondence |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9983204/ https://www.ncbi.nlm.nih.gov/pubmed/36869366 http://dx.doi.org/10.1186/s13045-023-01411-x |
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