E14a2 Transcript Favors Treatment-Free Remission in Chronic Myeloid Leukemia When Associated with Longer Treatment with Tyrosine Kinase Inhibitors and Sustained Deep Molecular Response

dc.contributor.authorMarcé, Sílvia
dc.contributor.authorMéndez, Aleix
dc.contributor.authorXicoy, Blanca
dc.contributor.authorEstrada, Natalia
dc.contributor.authorCabezón, Marta
dc.contributor.authorSturla, Antonella Luciana
dc.contributor.authorRatia García, Miriam
dc.contributor.authorAngona, Anna
dc.contributor.authorAmat, Paula
dc.contributor.authorEscribano Serrat, Silvia
dc.contributor.authorScalzulli, Emilia
dc.contributor.authorMorgades, Mireia
dc.contributor.authorSenín, Alicia
dc.contributor.authorHernández Boluda, Juan Carlos
dc.contributor.authorFerrer Marín, Francisca
dc.contributor.authorAnguita, Eduardo
dc.contributor.authorCortés, Montserrat
dc.contributor.authorPlensa, Esther
dc.contributor.authorBreccia, Massimo
dc.contributor.authorGarcía Gutiérrez, Valentín
dc.contributor.authorZamora, Lurdes
dc.date.accessioned2024-03-05T12:34:56Z
dc.date.available2024-03-05T12:34:56Z
dc.date.issued2024-01-29
dc.date.updated2024-02-26T12:50:43Z
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.format.extent12 p.
dc.format.mimetypeapplication/pdf
dc.identifier.issn2077-0383
dc.identifier.pmid38337473
dc.identifier.urihttps://hdl.handle.net/2445/208393
dc.language.isoeng
dc.publisherMDPI AG
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.3390/jcm13030779
dc.relation.ispartofJournal of Clinical Medicine, 2024, vol. 13, num. 3, p. 779
dc.relation.urihttps://doi.org/10.3390/jcm13030779
dc.rightscc by (c) Marcé, Sílvia et al., 2024
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.sourceArticles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
dc.subject.classificationLeucèmia mieloide
dc.subject.classificationInhibidors enzimàtics
dc.subject.otherMyeloid leukemia
dc.subject.otherEnzyme inhibitors
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.typeinfo:eu-repo/semantics/publishedVersion

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