<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Labrador J</submitter><funding>Instituto de Salud Carlos III</funding><pagination>1734</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8997036</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(7)</volume><pubmed_abstract>The effectiveness of venetoclax (VEN) in relapsed or refractory acute myeloid leukemia (RR-AML) has not been well established. This retrospective, multicenter, observational database studied the effectiveness of VEN in a cohort of 51 RR-AML patients and evaluated for predictors of response and overall survival (OS). The median age was 68 years, most were at high risk, 61% received ≥2 therapies for AML, 49% had received hypomethylating agents, and ECOG was ≥2 in 52%. Complete remission (CR) rate, including CR with incomplete hematological recovery (CRi), was 12.4%. Additionally, 10.4% experienced partial response (PR). The CR/CRi was higher in combination with azacitidine (AZA; 17.9%) than with decitabine (DEC; 6.7%) and low-dose cytarabine (LDAC; 0%). Mutated NPM1 was associated with incre</pubmed_abstract><journal>Cancers</journal><pubmed_title>Use of Venetoclax in Patients with Relapsed or Refractory Acute Myeloid Leukemia: The PETHEMA Registry Experience.</pubmed_title><pmcid>PMC8997036</pmcid><funding_grant_id>CD21/00022</funding_grant_id><pubmed_authors>Conde-Royo D</pubmed_authors><pubmed_authors>Foncillas MA</pubmed_authors><pubmed_authors>Recio I</pubmed_authors><pubmed_authors>Garcia-Fortes M</pubmed_authors><pubmed_authors>Cuello R</pubmed_authors><pubmed_authors>Sanz MA</pubmed_authors><pubmed_authors>de Laiglesia A</pubmed_authors><pubmed_authors>Vall-Llovera F</pubmed_authors><pubmed_authors>Olivier C</pubmed_authors><pubmed_authors>Seri-Merino C</pubmed_authors><pubmed_authors>Vives S</pubmed_authors><pubmed_authors>Munoz-Garcia C</pubmed_authors><pubmed_authors>Bienert-Garcia A</pubmed_authors><pubmed_authors>de Miguel D</pubmed_authors><pubmed_authors>Vidriales MB</pubmed_authors><pubmed_authors>Benzo-Callejo G</pubmed_authors><pubmed_authors>Sayas MJ</pubmed_authors><pubmed_authors>Labrador J</pubmed_authors><pubmed_authors>Perez-Encinas M</pubmed_authors><pubmed_authors>Sanchez-Sanchez MJ</pubmed_authors><pubmed_authors>Tormo M</pubmed_authors><pubmed_authors>Martinez-Cuadron D</pubmed_authors><pubmed_authors>Vahi M</pubmed_authors><pubmed_authors>Colorado M</pubmed_authors><pubmed_authors>Montesinos P</pubmed_authors><pubmed_authors>Rodriguez-Medina C</pubmed_authors><pubmed_authors>Roldan-Perez A</pubmed_authors><pubmed_authors>Saiz-Rodriguez M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Use of Venetoclax in Patients with Relapsed or Refractory Acute Myeloid Leukemia: The PETHEMA Registry Experience.</name><description>The effectiveness of venetoclax (VEN) in relapsed or refractory acute myeloid leukemia (RR-AML) has not been well established. This retrospective, multicenter, observational database studied the effectiveness of VEN in a cohort of 51 RR-AML patients and evaluated for predictors of response and overall survival (OS). The median age was 68 years, most were at high risk, 61% received ≥2 therapies for AML, 49% had received hypomethylating agents, and ECOG was ≥2 in 52%. Complete remission (CR) rate, including CR with incomplete hematological recovery (CRi), was 12.4%. Additionally, 10.4% experienced partial response (PR). The CR/CRi was higher in combination with azacitidine (AZA; 17.9%) than with decitabine (DEC; 6.7%) and low-dose cytarabine (LDAC; 0%). Mutated NPM1 was associated with incre</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Mar</publication><modification>2026-06-18T03:14:50.827Z</modification><creation>2025-04-04T12:40:59.55Z</creation></dates><accession>S-EPMC8997036</accession><cross_references><pubmed>35406512</pubmed><doi>10.3390/cancers14071734</doi></cross_references></HashMap>