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 ALL.
Introducing
Now you can personalise
your ALL Hub experience!
Bookmark content to read later
Select your specific areas of interest
View content recommended for you
Find out moreThe ALL 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 ALL Hub cannot guarantee the accuracy of translated content. The ALL 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 ALL Hub is an independent medical education platform, sponsored by Jazz Pharmaceuticals, Amgen, and Pfizer. 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.
Bookmark this article
During the 62nd American Society of Hematology (ASH) Annual Meeting and Exposition, the ALL Hub spoke to Andrea Biondi, University of Milano-Bicocca, Milan, IT. We asked, How do constitutively active signaling pathways impact response to treatment in pediatric T-cell ALL (T-ALL)?
How do constitutively active signaling pathways impact response to treatment in pediatric T-ALL?
Pediatric T-ALL accounts for 15% of total pediatric ALL cases. During the last 10 years, studies have focused on the deep analysis of genomic heterogeneities of T-ALL. In this podcast, Biondi discusses assessing molecular response as a predictive parameter for identifying the subgroup of patients with T-ALL with a dismal prognosis, and the constitutively active signaling pathways in pediatric T-ALL.
Your opinion matters
Subscribe to get the best content related to ALL delivered to your inbox