| Literature DB >> 29541231 |
Qian Li1, Xiao-Ji Lin2, Hui Chen1, Jian Gong1, Zhen Li3, Xiang-Nan Chen1.
Abstract
More than 90% of patients with chronic myeloid leukemia (CML) have the chromosomal translocation t(9;22)(q34;q11), while 5-8% of patients have complex variant translocations that have previously been thought not to affect the efficacy of imatinib therapy. The present study reports a patient with CML in B-lymphoid blast crisis who had a rare three-way Philadelphia (Ph) variant t(3;9;22)(p21;q34;q11), in addition to isodicentric Ph chromosomes. The patient was initially treated with imatinib for >2 months with a very poor response. When no T315I or F317L mutations in the ABL proto-oncogene 1 region were detected, the patient received dasatinib treatment (140 mg daily) and achieved a complete hematologic response. Following allo-hematopoietic stem cell transplantation, the patient displayed clinical, hematological and cytogenetic remission, with complete molecular response and complete donor chimerism, and stopped taking dasatinib at the last follow-up. The present data suggest that BCR-ABL gene amplification may be associated with imatinib resistance, which can be overcome with dasatinib. The present analysis suggests an alternative therapy strategy for CML involving isodicentric Ph chromosomes.Entities:
Keywords: chronic myelogenous leukemia; fluorescence in situ hybridization; imatinib resistance; isodicentric Ph chromosome; t(3,9,22)(p21;q34;q11)
Year: 2018 PMID: 29541231 PMCID: PMC5835883 DOI: 10.3892/ol.2018.7866
Source DB: PubMed Journal: Oncol Lett ISSN: 1792-1074 Impact factor: 2.967