ASCERTAIN Data: Oral Decitabine-Cedazuridine Outcomes in MDS

EP: 1.Advances in MDS Classification and Molecular Understanding

EP: 2.Choosing MDS Therapies: Risk-Based Approaches

EP: 3.Luspatercept in Lower Risk MDS: Insights on the COMMANDS Trial

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EP: 4.ASCERTAIN Data: Oral Decitabine-Cedazuridine Outcomes in MDS

EP: 5.Oral vs. Injectable HMAs: Convenience and Efficacy in Higher Risk MDS

EP: 6.HMA Persistence and Effectiveness in Higher Risk MDS

EP: 7.Innovations and Future Directions in Higher Risk MDS Treatments

EP: 8.Oral vs. Injectable HMAs: Patient Perspectives, Access, and IRA Impact

EP: 9.Oral vs. IV HMAs: Considerations and Patient Guidance

EP: 10.Patient Feedback for MDS: Insights and Closing Remarks

Video content above is prompted by the following:

• Although oral decitabine-cedazuridine has been FDA approved for some time, the ASCERTAIN trial data are a recent advancement in our knowledge of this drug and its use in myelodysplastic syndromes (MDS). Briefly describe the ASCERTAIN trial design.
• What are some key takeaways regarding the outcomes of treating MDS with oral decitabine-cedazuridine compared with intravenous decitabine, according to the ASCERTAIN data?