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 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 Astellas, Daiichi Sankyo, Johnson & Johnson, Kura Oncology and Syndax, and has been supported through educational grants from Bristol Myers Squibb and the Hippocrate Conference Institute, an association of the Servier Group. The 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
Andrés Gómez De LeónDuring the 2021 TCT Meetings Digital Experience, the AML Hub spoke to Andrés Gómez De León, Universidad Autónoma de Nuevo León, Monterrey, MX. We asked, What is the optimal timepoint for post-transplant MRD assessment?
What is the optimal timepoint for post-transplant MRD assessment?
Gómez De León discusses the association between Day +30 and +100 measurable residual disease (MRD) status and relapse following peripheral blood hematopoietic stem cell transplant (HSCT) in adult patients with high-risk acute leukemia.
Your opinion matters
Approximately what proportion of your patients with FLT3-mutations also have NPM1 and DNMT3A co-mutations?