<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ostronoff F</submitter><funding>NCI NIH HHS</funding><pagination>1157-64</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4372852</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>33(10)</volume><pubmed_abstract>&lt;h4>Purpose&lt;/h4>Younger patients with acute myeloid leukemia (AML) harboring NPM1 mutations without FLT3-internal tandem duplications (ITDs; NPM1-positive/FLT3-ITD-negative genotype) are classified as better risk; however, it remains uncertain whether this favorable classification can be applied to older patients with AML with this genotype. Therefore, we examined the impact of age on the prognostic significance of NPM1-positive/FLT3-ITD-negative status in older patients with AML.&lt;h4>Patients and methods&lt;/h4>Patients with AML age ≥ 55 years treated with intensive chemotherapy as part of Southwest Oncology Group (SWOG) and UK National Cancer Research Institute/Medical Research Council (NCRI/MRC) trials were evaluated. A comprehensive analysis first examined 156 patients treated in SWOG tria</pubmed_abstract><journal>Journal of clinical oncology : official journal of the American Society of Clinical Oncology</journal><pubmed_title>Prognostic significance of NPM1 mutations in the absence of FLT3-internal tandem duplication in older patients with acute myeloid leukemia: a SWOG and UK National Cancer Research Institute/Medical Research Council report.</pubmed_title><pmcid>PMC4372852</pmcid><funding_grant_id>T32 CA009515</funding_grant_id><funding_grant_id>CA12213</funding_grant_id><funding_grant_id>N01 CA032102</funding_grant_id><funding_grant_id>U10 CA180819</funding_grant_id><funding_grant_id>N01 CA038926</funding_grant_id><funding_grant_id>R01 CA160872</funding_grant_id><funding_grant_id>U10 CA032102</funding_grant_id><funding_grant_id>U10 CA073590</funding_grant_id><funding_grant_id>U10 CA020319</funding_grant_id><funding_grant_id>CA073590</funding_grant_id><funding_grant_id>CA160872</funding_grant_id><funding_grant_id>P01 CA018029</funding_grant_id><funding_grant_id>U10 CA038926</funding_grant_id><funding_grant_id>R01 CA114563</funding_grant_id><funding_grant_id>R25 CA174664</funding_grant_id><funding_grant_id>U10 CA180888</funding_grant_id><funding_grant_id>CA20319</funding_grant_id><funding_grant_id>U10 CA180828</funding_grant_id><pubmed_authors>Othus M</pubmed_authors><pubmed_authors>Godwin J</pubmed_authors><pubmed_authors>Stirewalt DL</pubmed_authors><pubmed_authors>Estey E</pubmed_authors><pubmed_authors>Evans A</pubmed_authors><pubmed_authors>Lazenby M</pubmed_authors><pubmed_authors>Pogosova-Agadjanyan EL</pubmed_authors><pubmed_authors>Oehler VG</pubmed_authors><pubmed_authors>Meshinchi S</pubmed_authors><pubmed_authors>Gilkes A</pubmed_authors><pubmed_authors>Radich JP</pubmed_authors><pubmed_authors>Willman CL</pubmed_authors><pubmed_authors>Kopecky KJ</pubmed_authors><pubmed_authors>List AF</pubmed_authors><pubmed_authors>Burnett A</pubmed_authors><pubmed_authors>Appelbaum FR</pubmed_authors><pubmed_authors>Ostronoff F</pubmed_authors><pubmed_authors>Fang M</pubmed_authors><pubmed_authors>Petersdorf SH</pubmed_authors></additional><is_claimable>false</is_claimable><name>Prognostic significance of NPM1 mutations in the absence of FLT3-internal tandem duplication in older patients with acute myeloid leukemia: a SWOG and UK National Cancer Research Institute/Medical Research Council report.</name><description>&lt;h4>Purpose&lt;/h4>Younger patients with acute myeloid leukemia (AML) harboring NPM1 mutations without FLT3-internal tandem duplications (ITDs; NPM1-positive/FLT3-ITD-negative genotype) are classified as better risk; however, it remains uncertain whether this favorable classification can be applied to older patients with AML with this genotype. Therefore, we examined the impact of age on the prognostic significance of NPM1-positive/FLT3-ITD-negative status in older patients with AML.&lt;h4>Patients and methods&lt;/h4>Patients with AML age ≥ 55 years treated with intensive chemotherapy as part of Southwest Oncology Group (SWOG) and UK National Cancer Research Institute/Medical Research Council (NCRI/MRC) trials were evaluated. A comprehensive analysis first examined 156 patients treated in SWOG tria</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Apr</publication><modification>2025-05-29T19:40:26.564Z</modification><creation>2025-05-29T19:40:26.564Z</creation></dates><accession>S-EPMC4372852</accession><cross_references><pubmed>25713434</pubmed><doi>10.1200/jco.2014.58.0571</doi><doi>10.1200/JCO.2014.58.0571</doi></cross_references></HashMap>