e14a2 Transcript Favors Treatment-Free Remission in Chronic Myeloid Leukemia When Associated with Longer Treatment with Tyrosine Kinase Inhibitors and Sustained Deep Molecular Response

被引:2
作者
Marce, Silvia [1 ]
Mendez, Aleix [1 ]
Xicoy, Blanca [1 ]
Estrada, Natalia [1 ]
Cabezon, Marta [1 ]
Sturla, Antonella Luciana [2 ]
Garcia, Miriam Ratia [2 ]
Angona, Anna [3 ]
Amat, Paula [4 ]
Escribano Serrat, Silvia [5 ]
Scalzulli, Emilia [6 ]
Morgades, Mireia [1 ]
Senin, Alicia [2 ]
Hernandez-Boluda, Juan Carlos [4 ]
Ferrer-Marin, Francisca [7 ]
Anguita, Eduardo [5 ]
Cortes, Montserrat [8 ]
Plensa, Esther [9 ]
Breccia, Massimo [6 ]
Garcia-Gutierrez, Valentin [10 ]
Zamora, Lurdes [1 ]
机构
[1] ICO Badalona Hosp Germans Trias i Pujol, Josep Carreras Leukaemia Res Inst IJC, Myeloid Neoplasms Grp, Hematol Dept, Badalona 08916, Spain
[2] ICO Hosp Hosp Duran y Reynals, Hematol Dept, Barcelona 08908, Spain
[3] ICO Girona Hosp Josep Trueta, Hematol Dept, Girona 17007, Spain
[4] Hosp Clin Univ INCLIVA Valencia, Hematol Dept, Valencia 46010, Spain
[5] Univ Complutense Madrid UCM, Hosp Clin San Carlos, Hematol Dept, IML,IdISSC, Madrid 28040, Spain
[6] Sapienza Univ, Dept Precis & Translat Med, Policlin Umberto 1, I-00189 Rome, Italy
[7] Hosp Gen Univ Morales Meseguer CIBERER, Hematol Dept, IMIB, UCAM, Murcia 30008, Spain
[8] Hosp Gen Granollers, Hematol Dept, Granollers 08402, Spain
[9] Hosp Mataro, Consorci Sanitari Maresme, Consorci Sanit Maresme, Mataro 08301, Spain
[10] Univ Alcalala Madrid, Hosp Ramon y Cajal, Hematol Dept, IRYCIS, Madrid 28801, Spain
关键词
chronic myeloid leukemia; BCR::ABL1 transcript type; tyrosine kinase inhibitors; discontinuation; treatment free remission; PROGNOSTIC DISCRIMINATION; IMATINIB; DISCONTINUATION; DASATINIB; NILOTINIB; THERAPY; RELAPSE; RISK;
D O I
10.3390/jcm13030779
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
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页数:12
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