Novel e4a2 BCR∷ABL1 transcript with insertion of CSE1L exons 9 and 10 in a CML patient: a case report

The <i>BCR::ABL1</i> fusion gene, resulting from the Philadelphia (Ph) chromosome, is the defining feature of Chronic Myeloid Leukemia (CML). The fusion transcript typically results from the juxtaposition of <i>ABL1</i> exons 2 or 3 and <i>BCR</i> exons 1, 13, 14 or 19, while exons 6 and 8 are less frequently involved. Here, we report the first case of a translocation in a patient with newly diagnosed chronic-phase CML harboring a novel e4a2 <i>BCR::ABL1</i> fusion gene. This unique fusion includes a 298 bp insertion, derived from a <i>CSE1L</i> gene exons 9 and 10, at the fusion site. The patient showed resistance to first-line dasatinib but achieved a molecular response with the third-generation tyrosine kinase inhibitor ponatinib.

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Publication Details

Journal
Frontiers in Oncology
Published
2025-08-13
DOI
https://doi.org/10.3389/fonc.2025.1596256
Primary Topic
Chronic Myeloid Leukemia Treatments
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article
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article

Novel e4a2 BCR∷ABL1 transcript with insertion of CSE1L exons 9 and 10 in a CML patient: a case report

Eleonora Toffoletti, Sara Di Giusto, Mario Tiribelli, Daniela Damiani et al.
Frontiers in Oncology
Chronic Myeloid Leukemia Treatments
article

Novel e4a2 BCR∷ABL1 transcript with insertion of CSE1L exons 9 and 10 in a CML patient: a case report

Eleonora Toffoletti, Sara Di Giusto, Mario Tiribelli, Daniela Damiani, Renato Fanin, Moira Moro, Cinzia Cozzarolo, Tomas Liani
article en

Abstract

The <i>BCR::ABL1</i> fusion gene, resulting from the Philadelphia (Ph) chromosome, is the defining feature of Chronic Myeloid Leukemia (CML). The fusion transcript typically results from the juxtaposition of <i>ABL1</i> exons 2 or 3 and <i>BCR</i> exons 1, 13, 14 or 19, while exons 6 and 8 are less frequently involved. Here, we report the first case of a translocation in a patient with newly diagnosed chronic-phase CML harboring a novel e4a2 <i>BCR::ABL1</i> fusion gene. This unique fusion includes a 298 bp insertion, derived from a <i>CSE1L</i> gene exons 9 and 10, at the fusion site. The patient showed resistance to first-line dasatinib but achieved a molecular response with the third-generation tyrosine kinase inhibitor ponatinib.

Frontiers in OncologyVol. 15
University of Udine (IT)
Openalex Percentile: Top 75%
Chronic Myeloid Leukemia Treatments
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