Please use this identifier to cite or link to this item: https://dipositint.ub.edu/dspace/handle/2445/208393
Title: E14a2 Transcript Favors Treatment-Free Remission in Chronic Myeloid Leukemia When Associated with Longer Treatment with Tyrosine Kinase Inhibitors and Sustained Deep Molecular Response
Author: Marcé, Sílvia
Méndez, Aleix
Xicoy, Blanca
Estrada, Natalia
Cabezón, Marta
Sturla, Antonella Luciana
García, Miriam Ratia
Angona, Anna
Amat, Paula
Escribano Serrat, Silvia
Scalzulli, Emilia
Morgades, Mireia
Senín, Alicia
Hernández-boluda, Juan Carlos
Ferrer-marín, Francisca
Anguita, Eduardo
Cortés, Montserrat
Plensa, Esther
Breccia, Massimo
García-gutierrez, Valentín
Zamora, Lurdes
Issue Date: 29-Jan-2024
Publisher: MDPI AG
Abstract: e13a2 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.
Note: Reproducció del document publicat a: https://doi.org/10.3390/jcm13030779
It is part of: Journal of Clinical Medicine, 2024, vol. 13, issue. 3, p. 779
URI: http://hdl.handle.net/2445/208393
Related resource: https://doi.org/10.3390/jcm13030779
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

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