Acute myeloid leukemia: current progress and future directions
- PMID: 33619261
- PMCID: PMC7900255
- DOI: 10.1038/s41408-021-00425-3
Acute myeloid leukemia: current progress and future directions
Abstract
Progress in the understanding of the biology and therapy of acute myeloid leukemia (AML) is occurring rapidly. Since 2017, nine agents have been approved for various indications in AML. These included several targeted therapies like venetoclax, FLT3 inhibitors, IDH inhibitors, and others. The management of AML is complicated, highlighting the need for expertise in order to deliver optimal therapy and achieve optimal outcomes. The multiple subentities in AML require very different therapies. In this review, we summarize the important pathophysiologies driving AML, review current therapies in standard practice, and address present and future research directions.
Conflict of interest statement
Dr. H.K. reports research grants and honoraria from AbbVie, Amgen, Ascentage, BMS, Daiichi-Sankyo, Immunogen, Jazz, Novartis, Pfizer, and Sanofi; honoraria from Actinium (Advisory Board), Adaptive Biotechnologies, Aptitude Health, BioAscend, Delta Fly, Janssen Global, Oxford Biomedical, and Takeda. Dr. T.K. reports grant or research support from BMS, Celgene, Pfizer, Amgen, Jazz, AstraZeneca, and Genetech; consultant fees from Agios, Jazz, Genetech, and Novartis. Dr. C.D. reports research support to institution from Abbvie, Agios, Bayer, Calithera, Cleave, BMS/Celgene, Daiichi-Sankyo and ImmuneOnc; consultant/advisory boards with Abbvie, Agios, Celgene/BMS, Daiichi-Sankyo, ImmuneOnc, Novartis, Takeda and Notable Labs. Dr. N.D. reports research funding from Daiichi-Sankyo, Bristol-Myers Squibb, Pfizer, Gilead, Sevier, Genentech, Astellas, Daiichi-Sankyo, Abbvie, Hanmi, Trovagene, FATE, Amgen, Novimmune, Glycomimetics, and ImmunoGen and has served in a consulting or advisory role for Daiichi-Sankyo, Bristol-Myers Squibb, Pfizer, Novartis, Celgene, AbbVie, Astellas, Genentech, Immunogen, Servier, Syndax, Trillium, Gilead, Amgen, and Agios. G.B. reports research funding from Bristol‐Myers Squibb, GlaxoSmithKline, Janssen Scientific Affairs, Eli Lilly and Company, Cyclacel, AstraZeneca, AbbVie, Oncoceutics, Arvinas, Cantargia, PTC Therapeutics, Argenx, BioTheryX, and Bioline and personal fees from PTC Therapeutics, Argenx, BioTheryX, and Bioline. Dr. E.J. reports research grants and advisory rolls with AbbVie, Adaptive Biotechnologies, Amgen, BMS, Pfizer and Takeda, and advisory roll with Genetech. Dr. M.K. reports grants and other from AbbVie, Genentech, F. Hoffman La-Roche, Stemline Therapeutics, Amgen, and Forty-Seven. G.G.‐M. has received grants from and acted in an advisory role for Celgene; has received grants and personal fees from Amphivena Therapeutics and Astex; and has received grants from Helsinn, Novartis, AbbVie, Onconova, H3 Biomedicine, and Merck for work performed outside of the current study. Dr. M.K. reports grants from Kisoji, Eli Lilly, Cellectis, Calithera, Ablynx, Agios, Ascentage, Astra Zeneca, other from Reata Pharmaceutical, Rafael Pharmaceutical, Sanofi. In addition, Dr. M.K. has US patents wityh Reara and Eli Lilly (US 7,795,305 B2 and a patent 62/993,166). Dr. F.R. reports research funding from BMS, Amgen, Xencor, Macrogenics, Orsenix, Abbvie, Prelude, Astex; consultancy and honoraria from Celgene, BMS, Amgen, Astellas, Xencor, Agios, AstraZeneca, and Orsenix.
Figures




Similar articles
-
Midostaurin/PKC412 for the treatment of newly diagnosed FLT3 mutation-positive acute myeloid leukemia.Expert Rev Hematol. 2017 Dec;10(12):1033-1045. doi: 10.1080/17474086.2017.1397510. Epub 2017 Oct 30. Expert Rev Hematol. 2017. PMID: 29069942 Review.
-
Updates on targeted therapies for acute myeloid leukaemia.Br J Haematol. 2022 Jan;196(2):316-328. doi: 10.1111/bjh.17746. Epub 2021 Aug 4. Br J Haematol. 2022. PMID: 34350585 Review.
-
Targeted therapies in Acute Myeloid Leukemia: a focus on FLT-3 inhibitors and ABT199.Expert Rev Hematol. 2017 Oct;10(10):863-874. doi: 10.1080/17474086.2017.1366852. Epub 2017 Aug 21. Expert Rev Hematol. 2017. PMID: 28799432 Review.
-
Tyrosine kinase inhibitors for acute myeloid leukemia: A step toward disease control?Blood Rev. 2020 Nov;44:100675. doi: 10.1016/j.blre.2020.100675. Epub 2020 Mar 2. Blood Rev. 2020. PMID: 32147087 Review.
-
The Future of Targeting FLT3 Activation in AML.Curr Hematol Malig Rep. 2017 Jun;12(3):153-167. doi: 10.1007/s11899-017-0381-2. Curr Hematol Malig Rep. 2017. PMID: 28421420 Review.
Cited by
-
Post-remission measurable residual disease directs treatment choice and improves outcomes for patients with intermediate-risk acute myeloid leukemia in CR1.Int J Hematol. 2022 Dec;116(6):892-901. doi: 10.1007/s12185-022-03441-6. Epub 2022 Aug 28. Int J Hematol. 2022. PMID: 36031670 Free PMC article.
-
Successful treatment of AML using non-intensive chemotherapy in Jehovah's Witness patients.Leuk Res Rep. 2024 Aug 8;22:100477. doi: 10.1016/j.lrr.2024.100477. eCollection 2024. Leuk Res Rep. 2024. PMID: 39238534 Free PMC article.
-
Global, national, and regional burden of acute myeloid leukemia among 60-89 years-old individuals: insights from a study covering the period 1990 to 2019.Front Public Health. 2024 Jan 11;11:1329529. doi: 10.3389/fpubh.2023.1329529. eCollection 2023. Front Public Health. 2024. PMID: 38274540 Free PMC article.
-
DNMT3A Mutation-Induced CDK1 Overexpression Promotes Leukemogenesis by Modulating the Interaction between EZH2 and DNMT3A.Biomolecules. 2021 May 22;11(6):781. doi: 10.3390/biom11060781. Biomolecules. 2021. PMID: 34067359 Free PMC article.
-
Therapeutic biomarkers in acute myeloid leukemia: functional and genomic approaches.Front Oncol. 2024 Feb 12;14:1275251. doi: 10.3389/fonc.2024.1275251. eCollection 2024. Front Oncol. 2024. PMID: 38410111 Free PMC article. Review.
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Miscellaneous