<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-07-06T10:36:11Z</responseDate><request verb="GetRecord" identifier="oai:docta.ucm.es:20.500.14352/72154" metadataPrefix="qdc">https://docta.ucm.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:docta.ucm.es:20.500.14352/72154</identifier><datestamp>2025-02-13T16:49:43Z</datestamp><setSpec>com_20.500.14352_14</setSpec><setSpec>col_20.500.14352_15</setSpec></header><metadata><qdc:qualifieddc xmlns:qdc="http://dspace.org/qualifieddc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://purl.org/dc/elements/1.1/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dc.xsd http://purl.org/dc/terms/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dcterms.xsd http://dspace.org/qualifieddc/ http://www.ukoln.ac.uk/metadata/dcmi/xmlschema/qualifieddc.xsd">
   <dc:title>Characteristics and Outcomes of Adult Patients in the PETHEMA Registry with Relapsed or Refractory FLT3-ITD Mutation-Positive Acute Myeloid Leukemia</dc:title>
   <dc:creator>Martínez Cuadrón, David</dc:creator>
   <dc:creator>Serrano, Josefina</dc:creator>
   <dc:creator>Mariz, José</dc:creator>
   <dc:creator>Gil, Cristina</dc:creator>
   <dc:creator>Tormo, Mar</dc:creator>
   <dc:creator>Martínez Sánchez, María Del Pilar</dc:creator>
   <dc:creator>Rodríguez Arbolí, Eduardo</dc:creator>
   <dc:creator>García Boyero, Raimundo</dc:creator>
   <dc:creator>Rodríguez Medina, Carlos</dc:creator>
   <dc:creator>Martínez Chamorro, Carmen</dc:creator>
   <dc:creator>Polo, Marta</dc:creator>
   <dc:creator>Bergua, Juan</dc:creator>
   <dc:creator>Aguiar, Eliana</dc:creator>
   <dc:creator>Amigo, María </dc:creator>
   <dc:creator>Herrera, Pilar</dc:creator>
   <dc:creator>Alonso Domínguez, Juan Manuel</dc:creator>
   <dc:creator>Bernal, Teresa</dc:creator>
   <dc:creator>Espadana, Ana</dc:creator>
   <dc:creator>Sayas, María </dc:creator>
   <dc:creator>Algarra, Lorenzo</dc:creator>
   <dc:creator>Vidriales, María B.</dc:creator>
   <dc:creator>Vasconcelos, Graça</dc:creator>
   <dc:creator>Vives, Susana</dc:creator>
   <dc:creator>Pérez Encinas, Manuel </dc:creator>
   <dc:creator>López, Aurelio</dc:creator>
   <dc:creator>Noriega Concepción, Víctor</dc:creator>
   <dc:creator>García Fortes, María</dc:creator>
   <dc:creator>Chillón, María </dc:creator>
   <dc:creator>Rodríguez Gutiérrez, Juan </dc:creator>
   <dc:creator>Calasanz, María</dc:creator>
   <dc:creator>Labrador, Jorge</dc:creator>
   <dc:creator>López, Juan</dc:creator>
   <dc:creator>Boluda, Blanca</dc:creator>
   <dc:creator>Rodríguez Veiga, Rebeca</dc:creator>
   <dc:creator>Martínez López, Joaquín</dc:creator>
   <dc:creator>Barragán, Eva</dc:creator>
   <dc:creator>Sanz, Miguel</dc:creator>
   <dc:creator>Montesinos, Pau</dc:creator>
   <dcterms:abstract>This retrospective study investigated outcomes of 404 patients with relapsed/refractory (R/R) FMS-like tyrosine kinase 3 (FLT3)-internal tandem duplication (ITD) acute myeloid leukemia (AML) enrolled in the PETHEMA registry, pre-approval of tyrosine kinase inhibitors. Most patients (63%) had received first-line intensive therapy with 3 + 7. Subsequently, patients received salvage with intensive therapy (n = 261), non-intensive therapy (n = 63) or supportive care only (n = 80). Active salvage therapy (i.e., intensive or non-intensive therapy) resulted in a complete remission (CR) or CR without hematological recovery (CRi) rate of 42%. More patients achieved a CR/CRi with intensive (48%) compared with non-intensive (19%) salvage therapy (p &lt; 0.001). In the overall population, median overall survival (OS) was 5.5 months; 1- and 5-year OS rates were 25% and 7%. OS was significantly (p &lt; 0.001) prolonged with intensive or non-intensive salvage therapy compared with supportive therapy, and in those achieving CR/CRi versus no responders. Of 280 evaluable patients, 61 (22%) had an allogeneic stem-cell transplant after they had achieved CR/CRi. In conclusion, in this large cohort study, salvage treatment approaches for patients with FLT3-ITD mutated R/R AML were heterogeneous. Median OS was poor with both non-intensive and intensive salvage therapy, with best long-term outcomes obtained in patients who achieved CR/CRi and subsequently underwent allogeneic stem-cell transplant.</dcterms:abstract>
   <dcterms:dateAccepted>2023-06-22T11:09:04Z</dcterms:dateAccepted>
   <dcterms:available>2023-06-22T11:09:04Z</dcterms:available>
   <dcterms:created>2023-06-22T11:09:04Z</dcterms:created>
   <dcterms:issued>2022</dcterms:issued>
   <dc:type>journal article</dc:type>
   <dc:identifier>https://hdl.handle.net/20.500.14352/72154</dc:identifier>
   <dc:identifier>2072-6694</dc:identifier>
   <dc:identifier>10.3390/cancers14112817</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>CB16/12/00284</dc:relation>
   <dc:rights>https://creativecommons.org/licenses/by/3.0/es/</dc:rights>
   <dc:rights>open access</dc:rights>
   <dc:rights>Atribución 3.0 España</dc:rights>
   <dc:publisher>MDPI</dc:publisher>
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