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 to access:
Bookmark & personalize site content
Receive alerts for new content in your areas of interest
View AML content recommended for you
Results from a multicenter, retrospective real-world analysis by the Programa Español de Tratamientos en Hematología (PETHEMA) group, evaluating fludarabine + cytarabine + granulocyte colony-stimulating factor + idarubicin (FLAG-Ida) as salvage therapy in adults with first relapsed/refractory (R/R) acute myeloid leukemia (AML; N = 1,079), were published in the American Journal of Hematology by Aspas Requena et al. The primary endpoint was overall survival (OS); secondary endpoints included complete remission composite (CRc), event-free survival (EFS), the proportion of patients proceeding to allogeneic hematopoietic stem cell transplantation (allo-HSCT), and validation of the SALFLAGE prognostic score.
Key data: At a median follow-up of 50.9 months, the median OS was 10.2 months (95% confidence interval [CI], 9.0–11.7) and the median EFS was 4.5 months. Overall, 56.8% of patients achieved a CRc, 8.4% died during induction, and 35.2% proceeded to allo-HSCT. By SALFLAGE scoring, median OS was 22.2, 13.4, and 6.9 months and CRc rates were 76.0%, 63.3%, and 42.2% in the low-, intermediate-, and high-risk groups, respectively (p < 0.001).
Key learning: FLAG-Ida is an effective salvage regimen for fit adults with R/R AML, enabling bridge-to-transplant in over one-third of patients, with the validated SALFLAGE score supporting risk-adapted salvage strategy selection.
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
Your opinion matters
Which AML-related topic do you currently need the most practical guidance on?