F359C mutation of the BCR-ABL1 gene in adolescent with chronic myeloid leukemia. Case report

Author:

Borisevich M. V.1ORCID,Savitskaya T. V.1

Affiliation:

1. Republican Scientific and Practical Center for Pediatric Oncology, Hematology and Immunology, Ministry of Health of the Republic of Belarus

Abstract

Chronic myeloid leukemia (CML) in children is rare, less than 3 % of all cases of leukemia in pediatric practice. Along with the successes achieved in the treatment of CML with imatinib, it’s necessary to study of molecular factors in predicting resistance to therapy. According to the literature, about 30 % of adult patients with imatinib resistance have point mutations in the kinase domain of BCR-ABL1 gene. The number of reports about mutation spectrum of the BCR-ABL1 gene in children with resistant forms of CML is limited. This article describes the clinical case of secondary resistance to imatinib in a 15-year-old girl with the F359C mutation of BCR-ABL1 gene and a review of the literature.

Publisher

OOO Grafika

Subject

Oncology,Hematology,Pediatrics, Perinatology, and Child Health

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