Newly Diagnosed Patients With AML: Discussing Implications of Recent Trial Results

EP: 1.Overview of Pathophysiology of and Progression of AML

EP: 2.Risk Classification Systems in AML

EP: 3.Key Patient Factors to Consider in AML Treatment Decisions

EP: 4.Provider Perspectives on Biggest Unmet Needs in AML Care

EP: 5.Social Determinants to AML Treatment Approach

EP: 6.Latest NCCN Guidelines on the Standard of Care for Patients With AML

EP: 7.Patient Eligibility for Transplant, Induction, and Consolidation in AML Treatment

EP: 8.Venetoclax and the Impact on Management of Older Patients With AML

EP: 9.Combination Therapies in AML Treatment Approach

EP: 10.Tracking the Shifting Treatment Landscape of AML

EP: 11.Expert Perspectives on IDH Inhibitors in AML Treatment

EP: 12.Managing Toxicities in Patients With AML

EP: 13.Comparing Safety and Efficacy of Novel AML Agents Against Established Regimens

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EP: 14.Newly Diagnosed Patients With AML: Discussing Implications of Recent Trial Results

Patients with newly diagnosed acute myeloid leukemia (AML) now have access to oral decitabine/cedazuridine combinations that provide equivalent efficacy to intravenous hypomethylating agents while offering significant convenience advantages. The oral formulation combines decitabine with cedazuridine, which inhibits the enzyme responsible for drug breakdown, extending the medication’s half-life and allowing for oral administration with bioavailability equivalent to intravenous therapy. This development represents a major advance for patients who previously required daily clinic visits for multiple consecutive days each treatment cycle.

The transition to oral hypomethylating agents particularly benefits patients in complex treatment regimens involving multiple targeted therapies, as it eliminates the need for frequent intravenous administrations while maintaining treatment effectiveness. Patients with multiple genetic mutations may receive combination regimens including oral hypomethylating agents, venetoclax, IDH inhibitors, FLT3 inhibitors, or menin inhibitors, creating comprehensive oral treatment programs that were impossible with previous generation therapies. This shift allows patients to manage sophisticated multidrug regimens from home while maintaining regular monitoring and support from their health care teams.

However, patients face new challenges with all-oral regimens, including complex medication management, potential drug interactions, insurance coverage issues, and adherence requirements that differ significantly from clinic-administered treatments. Health care teams must develop new systems for monitoring patient adherence, managing adverse effects remotely, and ensuring patients understand proper medication timing and food interactions. The convenience benefits of oral therapy must be balanced against the need for robust patient education, family involvement in medication management, and close monitoring systems to ensure treatment effectiveness while maintaining patient safety throughout their treatment journey.