<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>145(17)</volume><submitter>Mantzaris I</submitter><pubmed_abstract>&lt;h4>Abstract&lt;/h4>Venetoclax (Ven), when combined with intensive chemotherapy, shows promise for untreated acute myeloid leukemia (AML), but its integration with the 7+3 regimen remains underexplored. In a phase 1b study, we assessed the safety and efficacy of Ven with daunorubicin and cytarabine in patients with newly diagnosed AML. A total of 34 patients (median age, 59 years; 62% non-White) received Ven at escalating durations (8, 11, or 14 days). Adverse events included febrile neutropenia (100%), sepsis (29%), and enterocolitis (23.5%), but there were no induction deaths. The median recovery times for neutrophils (>1.0 × 103/μL) and platelets (>100 × 103/μL) were less than 30 days. Composite complete remission was achieved in 85.3% of patients, and 86.2% were negative for measurable re</pubmed_abstract><journal>Blood</journal><pagination>1870-1875</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12060153</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Venetoclax plus daunorubicin and cytarabine for newly diagnosed acute myeloid leukemia: results of a phase 1b study.</pubmed_title><pmcid>PMC12060153</pmcid><pubmed_authors>Kornblum NS</pubmed_authors><pubmed_authors>Shah L</pubmed_authors><pubmed_authors>Verceles JA</pubmed_authors><pubmed_authors>Tirone B</pubmed_authors><pubmed_authors>Shah N</pubmed_authors><pubmed_authors>Fehn K</pubmed_authors><pubmed_authors>Mantzaris I</pubmed_authors><pubmed_authors>Sica RA</pubmed_authors><pubmed_authors>Shapiro L</pubmed_authors><pubmed_authors>Goldfinger M</pubmed_authors><pubmed_authors>Kim M</pubmed_authors><pubmed_authors>Feldman EJ</pubmed_authors><pubmed_authors>Cooper DL</pubmed_authors><pubmed_authors>Dhawan A</pubmed_authors><pubmed_authors>Uriel M</pubmed_authors><pubmed_authors>Verma A</pubmed_authors><pubmed_authors>Konopleva M</pubmed_authors><pubmed_authors>Shastri A</pubmed_authors><pubmed_authors>Gritsman K</pubmed_authors><pubmed_authors>Munoz A</pubmed_authors><pubmed_authors>Zhang C</pubmed_authors><pubmed_authors>Chambers N</pubmed_authors><pubmed_authors>Clark S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Venetoclax plus daunorubicin and cytarabine for newly diagnosed acute myeloid leukemia: results of a phase 1b study.</name><description>&lt;h4>Abstract&lt;/h4>Venetoclax (Ven), when combined with intensive chemotherapy, shows promise for untreated acute myeloid leukemia (AML), but its integration with the 7+3 regimen remains underexplored. In a phase 1b study, we assessed the safety and efficacy of Ven with daunorubicin and cytarabine in patients with newly diagnosed AML. A total of 34 patients (median age, 59 years; 62% non-White) received Ven at escalating durations (8, 11, or 14 days). Adverse events included febrile neutropenia (100%), sepsis (29%), and enterocolitis (23.5%), but there were no induction deaths. The median recovery times for neutrophils (>1.0 × 103/μL) and platelets (>100 × 103/μL) were less than 30 days. Composite complete remission was achieved in 85.3% of patients, and 86.2% were negative for measurable re</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Apr</publication><modification>2026-06-01T05:58:44.177Z</modification><creation>2026-04-08T09:46:48.203Z</creation></dates><accession>S-EPMC12060153</accession><cross_references><pubmed>39919267</pubmed><doi>10.1182/blood.2024026700</doi></cross_references></HashMap>