<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9(7)</volume><submitter>Fraccaroli A</submitter><pubmed_abstract>&lt;h4>Abstract&lt;/h4>Whether patients with acute myeloid leukemia (AML) harboring nucleophosmin mutations (NPM1mut) and measurable residual disease (MRD) should undergo allogeneic stem cell transplantation (allo-SCT) in complete remission (CR) remains debatable. This study assessed whether bone marrow (BM) NPM1mut MRD, detected via quantitative reverse transcription polymerase chain reaction (qRT-PCR) with 10-5 sensitivity, influences allo-SCT benefit. Data from 4 German transplantation centers included 174 patients with AML NPM1mut who underwent first allo-SCT between 2011 and 2022. Among 122 patients transplanted in CR, pre-allo-SCT MRD was positive in 54%. After allo-SCT, BM MRD negativity increased from 65% (day +30) to 73% (day +100), with FMS-like tyrosine kinase 3-internal tandem duplic</pubmed_abstract><journal>Blood advances</journal><pagination>1630-1641</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11995096</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Pretransplant MRD does not seem to affect survival in NPM1-mutated AML undergoing allogeneic stem cell transplantation.</pubmed_title><pmcid>PMC11995096</pmcid><pubmed_authors>Schmid C</pubmed_authors><pubmed_authors>Spiekermann K</pubmed_authors><pubmed_authors>Hirschbuhl K</pubmed_authors><pubmed_authors>Haebe S</pubmed_authors><pubmed_authors>Herold T</pubmed_authors><pubmed_authors>Drolle H</pubmed_authors><pubmed_authors>Jurinovic V</pubmed_authors><pubmed_authors>Verbeek M</pubmed_authors><pubmed_authors>Tischer J</pubmed_authors><pubmed_authors>Koch K</pubmed_authors><pubmed_authors>Breitkopf S</pubmed_authors><pubmed_authors>Dufour A</pubmed_authors><pubmed_authors>Metzeler KH</pubmed_authors><pubmed_authors>Hentrich M</pubmed_authors><pubmed_authors>Fraccaroli A</pubmed_authors><pubmed_authors>Hausmann A</pubmed_authors><pubmed_authors>Rothenberg-Thurley M</pubmed_authors><pubmed_authors>Stauffer E</pubmed_authors></additional><is_claimable>false</is_claimable><name>Pretransplant MRD does not seem to affect survival in NPM1-mutated AML undergoing allogeneic stem cell transplantation.</name><description>&lt;h4>Abstract&lt;/h4>Whether patients with acute myeloid leukemia (AML) harboring nucleophosmin mutations (NPM1mut) and measurable residual disease (MRD) should undergo allogeneic stem cell transplantation (allo-SCT) in complete remission (CR) remains debatable. This study assessed whether bone marrow (BM) NPM1mut MRD, detected via quantitative reverse transcription polymerase chain reaction (qRT-PCR) with 10-5 sensitivity, influences allo-SCT benefit. Data from 4 German transplantation centers included 174 patients with AML NPM1mut who underwent first allo-SCT between 2011 and 2022. Among 122 patients transplanted in CR, pre-allo-SCT MRD was positive in 54%. After allo-SCT, BM MRD negativity increased from 65% (day +30) to 73% (day +100), with FMS-like tyrosine kinase 3-internal tandem duplic</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Apr</publication><modification>2025-07-03T03:06:45.093Z</modification><creation>2025-07-03T03:06:45.093Z</creation></dates><accession>S-EPMC11995096</accession><cross_references><pubmed>39903105</pubmed><doi>10.1182/bloodadvances.2024014767</doi></cross_references></HashMap>