TY - JOUR
T1 - e14a2 Transcript Favors Treatment-Free Remission in Chronic Myeloid Leukemia When Associated with Longer Treatment with Tyrosine Kinase Inhibitors and Sustained Deep Molecular Response
AU - Marcé, Silvia
AU - Méndez, Aleix
AU - Xicoy, Blanca
AU - Estrada, Natalia
AU - Cabezón, Marta
AU - Sturla, Antonella Luciana
AU - García, Miriam Ratia
AU - Angona, Anna
AU - Amat, Paula
AU - Universidad Complutense de Madrid, null
AU - Scalzulli, Emilia
AU - Morgades, Mireia
AU - Senín, Alicia
AU - Hernandez-Boluda, Juan Carlos
AU - Ferrer-Marín, Francisca
AU - Anguita, Eduardo
AU - Cortés, Montserrat
AU - Plensa, Esther
AU - Breccia, M.
AU - Garcia-Gutierrez, Valentin
AU - Zamora, Lurdes
PY - 2024/1/29
Y1 - 2024/1/29
N2 - 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.
AB - 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.
KW - chronic myeloid leukemia
KW - BCR::ABL1 transcript type
KW - tyrosine kinase inhibitors
KW - discontinuation
KW - treatment free remission
UR - https://www.scopus.com/pages/publications/85184706948
UR - https://www.mendeley.com/catalogue/75475e97-8716-3e8c-910f-a51b8aa34c26/
U2 - 10.3390/jcm13030779
DO - 10.3390/jcm13030779
M3 - Article
C2 - 38337473
SN - 2077-0383
VL - 13
JO - Journal of Clinical Medicine
JF - Journal of Clinical Medicine
IS - 3
M1 - 779
ER -