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dc.contributorHospital General de Granollers
dc.contributor.authorMARCE, Silvia
dc.contributor.authorMéndez, Aleix
dc.contributor.authorXicoy, Blanca
dc.contributor.authorEstrada, Natalia
dc.contributor.authorCabezón, Marta
dc.contributor.authorSturla, Antonella Luciana
dc.contributor.authorCortes, Montse
dc.date.accessioned2024-04-03T08:41:07Z
dc.date.available2024-04-03T08:41:07Z
dc.date.issued2024-01-29
dc.identifier.citationMarcé S, Méndez A, Xicoy B, Estrada N, Cabezón M, Sturla AL, et al. e14a2 Transcript Favors Treatment-Free Remission in Chronic Myeloid Leukemia When Associated with Longer Treatment with Tyrosine Kinase Inhibitors and Sustained Deep Molecular Response. J Clin Med. 2024 Jan 29;13(3):779.
dc.identifier.urihttps://hdl.handle.net/11351/11277
dc.descriptionBCR-ABL fusion gene; Chronic myeloid leukemia; Tyrosine kinase inhibitors
dc.description.abstracte13a2 and e14a2 are the most frequent transcript types of the BCR::ABL1 fusion gene in chronic myeloid leukemia (CML). The current goal with tyrosine kinase inhibitors (TKI) is to achieve sustained deep molecular response (DMR) in order to discontinue TKI treatment and remain in the so-called treatment-free remission (TFR) phase, but biological factors associated with these goals are not well established. This study aimed to determine the effect of transcript type on TFR in patients receiving frontline treatment with imatinib (IM) or second-generation TKI (2G-TKI). Patients treated at least 119 months with IM presented less post-discontinuation relapse than those that discontinued IM before 119 months (p = 0.005). In addition, cases with the e14a2 transcript type treated at least 119 months with IM presented a better TFR (p = 0.024). On the other hand, the type of transcript did not affect the cytogenetic or molecular response in 2G-TKI treated patients; however, the use of 2G-TKI may be associated with higher and earlier DMR in patients with the e14a2 transcript.
dc.language.isoeng
dc.publisherMDPI
dc.relation.ispartofseriesJournal of Clinical Medicine;13(3)
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceScientia
dc.subjectLeucèmia mieloide crònica
dc.subjectProteïnes quinases - Inhibidors
dc.subjectMedicaments antineoplàstics
dc.subject.meshLeukemia, Myeloid, Chronic-Phase
dc.subject.meshProtein Kinase Inhibitors
dc.subject.meshLeukemia, Myelogenous, Chronic, BCR-ABL Positive
dc.titlee14a2 Transcript Favors Treatment-Free Remission in Chronic Myeloid Leukemia When Associated with Longer Treatment with Tyrosine Kinase Inhibitors and Sustained Deep Molecular Response
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.3390/jcm13030779
dc.subject.decsleucemia mieloide de fase crónica
dc.subject.decsinhibidores de proteínas cinasas
dc.subject.decsleucemia mielogenosa crónica BCR-ABL positiva
dc.relation.publishversionhttps://doi.org/10.3390/jcm13030779
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.authoraffiliation[Marcé S, Méndez A, Xicoy B, Estrada N, Cabezón M] Hematology Department, Myeloid Neoplasms Group, ICO Badalona-Hospital Germans Trias i Pujol, Josep Carreras Leukaemia Research Institute (IJC), Badalona, Spain. [Sturla AL] Hematology Department, ICO Hospitalet-Hospital Duran y Reynals, Barcelona, Spain. [Cortés M] Hematology Department, Hospital General de Granollers, Granollers, Spain
dc.identifier.pmid38337473
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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