In a randomized phase 2 trial involving adults with AML, azacitidine–venetoclax led to longer event-free survival than induction chemotherapy, with a lower risk of severe infection and hemorrhage. Full PARADIGM trial results: https://t.co/iiDNsw6CUW
Editorial: Hypomethylating Agents plus Venetoclax as Compared with Intensive Chemotherapy in Patients with AML https://t.co/zsAPQjxEDb
A landmark pre-clinical study in @Nature shows in vivo mRNA delivery to HSPCs through a lipid nanoparticule conjugated to anti-CD34 can lead to efficient editing w/ gene function restoration w/o perturbing hematopoiesis - a leap into the future!
https://t.co/jNHOsFUQbx
CONGRESS | #EHA2026 | POSTER
Cecilia Arana Yi presents real-world outcomes of patients with MECOMr AML from the COMMAND MARROW consortium, and Flatiron database.
In this population, survival was poor and half of responders relapsed. Intensive chemotherapy resulted in higher remission rates vs HMAs or HMA+Venetoclax. These findings confirm the need for improved treatment strategies for this AML subtype.
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#AMLsm #leusm #MedicalCongress #MedNews #MedEd @Dr_Cecilia_Yi@MayoClinic
#EHA2026#AML#leusm
Dr. Barote: OPTI-AML: the first prospective RCT of Ven 14d vs 28d + Aza ×2 cycles in older AML — and it reframes the whole “shorter is fine” debate.
AV14 did NOT meet non-inferiority for CR (43% vs 49% AV28; ΔCI –8% to +21%, upper bound >10%).
Key takeaways 👇🏽
But the real story is molecular, not calendar:
• NPM1 & IDH1/2 → favored 28d (61% vs 42%)
• Every other subset → 44% vs 44%, identical
And cumulative delivery, not the planned schedule, tracked with response: pts who couldn’t complete Ven had lower CR in BOTH arms (AV28 39% vs 56%; AV14 36% vs 49%). Only 68% of AV28 finished C1 Ven (vs 89%) — mostly infections.
MRD negativity (78% vs 77%) and toxicity were superimposable. OS numerically favored AV28 but on MVA was driven by TP53/KRAS + counts, not arm.
Bottom line: Ven duration should be titrated to molecular subtype + triplet partner — what matters is cumulative exposure delivered, and for NPM1/IDH that exposure still earns its keep. #EHA2026 #EHA26
Incredible moment in the history of AML therapeutics. The prospect of all oral, all outpatient AML treatment is a reality now and all future therapeutics will be judged against this standard.
🚨 The FDA approved oral decitabine and cedazuridine tablets with venetoclax for newly diagnosed AML in adults ≥75 years, or who have comorbidities that preclude the use of intensive induction chemotherapy.
https://t.co/z8MRDvataW
#leusm#AML#leukemia#oncology | @FDAOncology
🚨 The FDA approved oral decitabine and cedazuridine tablets with venetoclax for newly diagnosed AML in adults ≥75 years, or who have comorbidities that preclude the use of intensive induction chemotherapy.
https://t.co/z8MRDvataW
#leusm#AML#leukemia#oncology | @FDAOncology
In this large retrospective study of FLT3-mutated AML, we confirm the important role of FLT3 inhibitors in intensively treated pts and demonstrate promising outcomes w/ low-intensity triplets in older/unfit pts.
@MDAndersonNews#Leukemia@JournalCancer
https://t.co/OZy6PCMCjD
Neutrophil recovery is quick, happening in 15 days, and sustained in IDH1 mutant R/R MDS. Happy to have reported on this data at #ASH2024. Thanks to all my co investigators and patients who took part in this study.
https://t.co/Y6JoNai4sO