<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Yang YL</submitter><funding>Ministry of Science and Technology, Taiwan</funding><pagination>5893</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7960737</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(1)</volume><pubmed_abstract>Improvement in outcomes of children with acute myeloid leukemia (AML) is attributed to several refinements in clinical management. We evaluated treatment outcomes of Taiwanese pediatric AML patients in the past 20 years. Overall, 860 de novo AML patients aged 0-18 years and registered in the Childhood Cancer Foundation of R.O.C during January 1996-December 2019 were included. Survival analysis was performed to identify factors that improved treatment outcomes. Regardless of treatment modalities used, patients during 2008-2019 had better 5-year event-free survival (EFS) and overall survival (OS) rates than patients during 1996-2007. For patients received the TPOG-AML-97A treatment, only 5-year OS rates were significantly different between patients diagnosed before and after 2008. Patients w</pubmed_abstract><journal>Scientific reports</journal><pubmed_title>Treatment outcomes of pediatric acute myeloid leukemia: a retrospective analysis from 1996 to 2019 in Taiwan.</pubmed_title><pmcid>PMC7960737</pmcid><funding_grant_id>MOST-109023140B0002-156</funding_grant_id><pubmed_authors>Chen JS</pubmed_authors><pubmed_authors>Wu KH</pubmed_authors><pubmed_authors>Yen HJ</pubmed_authors><pubmed_authors>Yang CP</pubmed_authors><pubmed_authors>Hsiao CC</pubmed_authors><pubmed_authors>Lin KH</pubmed_authors><pubmed_authors>Ho WL</pubmed_authors><pubmed_authors>Chen YC</pubmed_authors><pubmed_authors>Jou ST</pubmed_authors><pubmed_authors>Hung GY</pubmed_authors><pubmed_authors>Peng CT</pubmed_authors><pubmed_authors>Yeh TC</pubmed_authors><pubmed_authors>Liu HC</pubmed_authors><pubmed_authors>Chen RL</pubmed_authors><pubmed_authors>Lin MT</pubmed_authors><pubmed_authors>Wang JL</pubmed_authors><pubmed_authors>Weng TF</pubmed_authors><pubmed_authors>Chao YH</pubmed_authors><pubmed_authors>Chang YH</pubmed_authors><pubmed_authors>Lu MY</pubmed_authors><pubmed_authors>Huang FL</pubmed_authors><pubmed_authors>Liang DC</pubmed_authors><pubmed_authors>Wang LY</pubmed_authors><pubmed_authors>Wang SC</pubmed_authors><pubmed_authors>Sheen JM</pubmed_authors><pubmed_authors>Chao YY</pubmed_authors><pubmed_authors>Hou JY</pubmed_authors><pubmed_authors>Cheng SN</pubmed_authors><pubmed_authors>Lin CY</pubmed_authors><pubmed_authors>Chang HH</pubmed_authors><pubmed_authors>Chang TT</pubmed_authors><pubmed_authors>Chou SW</pubmed_authors><pubmed_authors>Jaing TH</pubmed_authors><pubmed_authors>Lin DT</pubmed_authors><pubmed_authors>Huang TH</pubmed_authors><pubmed_authors>Chang TK</pubmed_authors><pubmed_authors>Chen HY</pubmed_authors><pubmed_authors>Yang SH</pubmed_authors><pubmed_authors>Yang YL</pubmed_authors><pubmed_authors>Chen SH</pubmed_authors><pubmed_authors>Chen BW</pubmed_authors><pubmed_authors>Hung IJ</pubmed_authors><pubmed_authors>Cheng CN</pubmed_authors><pubmed_authors>Hsieh YL</pubmed_authors></additional><is_claimable>false</is_claimable><name>Treatment outcomes of pediatric acute myeloid leukemia: a retrospective analysis from 1996 to 2019 in Taiwan.</name><description>Improvement in outcomes of children with acute myeloid leukemia (AML) is attributed to several refinements in clinical management. We evaluated treatment outcomes of Taiwanese pediatric AML patients in the past 20 years. Overall, 860 de novo AML patients aged 0-18 years and registered in the Childhood Cancer Foundation of R.O.C during January 1996-December 2019 were included. Survival analysis was performed to identify factors that improved treatment outcomes. Regardless of treatment modalities used, patients during 2008-2019 had better 5-year event-free survival (EFS) and overall survival (OS) rates than patients during 1996-2007. For patients received the TPOG-AML-97A treatment, only 5-year OS rates were significantly different between patients diagnosed before and after 2008. Patients w</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Mar</publication><modification>2025-04-22T10:51:52.826Z</modification><creation>2025-04-05T23:40:16.965Z</creation></dates><accession>S-EPMC7960737</accession><cross_references><pubmed>33723338</pubmed><doi>10.1038/s41598-021-85321-3</doi></cross_references></HashMap>