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 moreCreate an account and access these new features:
Bookmark content to read later
Select your specific areas of interest
View aml content recommended for you
Video series
During a meeting of the AML Hub Steering Committee, held on May 8, 2024, Jeffrey Lancet chaired a discussion on the question: How can we intervene with measurable residual disease (MRD)-directed therapy within and outside of transplantation? This featured contributions from Charles Craddock, Gail Roboz, and Yasushi Miyazaki.
Lancet discusses the use of MRD-directed therapy, particularly in patients with MRD-positive disease, and the strategies for those transitioning from MRD positivity to negativity. The discussion includes insights from the QUAZAR study and raises concerns about the reliability of measuring MRD conversion, especially with flow cytometry. Risk stratification at diagnosis was also addressed, focusing on countries where MRD assessment for AML is not well established. The steering committee members recognize the unmet need to establish MRD as a definitive endpoint in clinical trials and to research the optimal timing for post-transplant MRD assessment.