All content on this site is intended for healthcare professionals only. By acknowledging this message and accessing the information on this website you are confirming that you are a healthcare professional. If you are a patient or carer, please visit Know AML.
The AML Hub website uses a third-party service provided by Google that dynamically translates web content. Translations are machine generated, so may not be an exact or complete translation, and the AML Hub cannot guarantee the accuracy of translated content. The AML Hub and its employees will not be liable for any direct, indirect, or consequential damages (even if foreseeable) resulting from use of the Google Translate feature. For further support with Google Translate, visit Google Translate Help.
The AML Hub is an independent medical education platform, sponsored by Daiichi Sankyo, Johnson & Johnson, Syndax, Thermo Fisher Scientific, Kura Oncology, and AbbVie. Funders are allowed no direct influence on our content. The levels of sponsorship listed are reflective of the amount of funding given. View funders.
Now you can support HCPs in making informed decisions for their patients
Your contribution helps us continuously deliver expertly curated content to HCPs worldwide. You will also have the opportunity to make a content suggestion for consideration and receive updates on the impact contributions are making to our content.
Find out more
Create an account and access these new features:
Bookmark content to read later
Select your specific areas of interest
View AML content recommended for you
A modified Delphi consensus on the management of patients with FLT3-mutated acute myeloid leukemia (AML), from a panel of eight Italian hematology experts, was recently published in Cancers by Olivieri et al. The aim of this consensus was to provide best practice recommendations for diagnosing and treating FLT3-mutated AML.
Key data: High consensus (≥80% agreement) was achieved across all statements in a single voting round. Key recommendations include testing for both FLT3-internal tandem duplication (ITD) and FLT3-tyrosine kinase domain (TKD) mutations at diagnosis, with capillary electrophoresis as the preferred method. All fit patients should receive intensive chemotherapy (IC) + an FLT3 inhibitor; additionally, all fit patients with FLT3‑ITD AML should be evaluated for allogeneic hematopoietic stem cell transplantation (allo‑HSCT) eligibility. Hypomethylating agent + venetoclax is considered suboptimal for unfit patients with FLT3‑ITD AML. Measurable residual disease (MRD) monitoring is recommended to guide transplant decisions. Retesting FLT3 is recommended for relapsed/refractory (R/R) disease, and gilteritinib is the preferred treatment option in this population.
Key learning: This consensus provides recommendations, based on clinical data, for mutation testing and therapeutic options for FLT3-mutated AML, supporting consistent management across institutions.
References
Please indicate your level of agreement with the following statements:
The content was clear and easy to understand
The content addressed the learning objectives
The content was relevant to my practice
I will change my clinical practice as a result of this content