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 Sílvia1ORCID,Méndez Aleix1,Xicoy Blanca1ORCID,Estrada Natalia1,Cabezón Marta1,Sturla Antonella Luciana2,García Miriam Ratia2,Angona Anna3,Amat Paula4,Escribano Serrat Silvia5ORCID,Scalzulli Emilia6,Morgades Mireia1,Senín Alicia2,Hernández-Boluda Juan Carlos4ORCID,Ferrer-Marín Francisca7,Anguita Eduardo5ORCID,Cortés Montserrat8,Plensa Esther9,Breccia Massimo6ORCID,García-Gutierrez Valentín10ORCID,Zamora Lurdes1ORCID

Affiliation:

1. Hematology Department, Myeloid Neoplasms Group, ICO Badalona-Hospital Germans Trias i Pujol, Josep Carreras Leukaemia Research Institute (IJC), 08916 Badalona, Spain

2. Hematology Department, ICO Hospitalet-Hospital Duran y Reynals, 08908 Barcelona, Spain

3. Hematology Department, ICO Girona-Hospital Josep Trueta, 17007 Girona, Spain

4. Hematology Department, Hospital Clínico Universitario-INCLIVA de Valencia, 46010 Valencia, Spain

5. Hematology Department, Hospital Clínico San Carlos, IML, IdISSC, Universidad Complutense de Madrid (UCM), 28040 Madrid, Spain

6. Hematology, Department of Precision and Translational Medicine, Policlinico Umberto 1, Sapienza University, 00189 Rome, Italy

7. Hematology Department, Hospital General Universitario Morales Meseguer-CIBERER, IMIB, UCAM, 30008 Múrcia, Spain

8. Hematology Department, Hospital General de Granollers, 08402 Granollers, Spain

9. Hematology Department, Consorci Sanitari del Maresme, Hospital de Mataró, 08301 Mataró, Spain

10. Hematology Department, Hospital Ramón y Cajal, IRYCIS, Universidad de Alcalalá Madrid, 28801 Madrid, Spain

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.

Funder

GRC) Generalitat de Catalunya

CERCA Programme/Generalitat de Catalunya

Josep Carreras International Foundation

“La Caixa” Foundation

Publisher

MDPI AG

Subject

General Medicine

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