A Rare t(9;22;16)(q34;q11;q24) Translocation in Chronic Myeloid Leukemia for Which Imatinib Mesylate Was Effective: A Case Report
Author(s) -
Masahiro Manabe,
Yumi Yoshii,
Satoru Mukai,
Erina Sakamoto,
Hiroshi Kanashima,
Takeshi Inoue,
Hirofumi Teshima
Publication year - 2011
Publication title -
leukemia research and treatment
Language(s) - English
Resource type - Journals
eISSN - 2090-3219
pISSN - 2090-3227
DOI - 10.4061/2011/592519
Subject(s) - chromosomal translocation , imatinib mesylate , myeloid leukemia , imatinib , trisomy 8 , philadelphia chromosome , karyotype , cancer research , medicine , biology , chromosome , genetics , gene
The t(9;22)(q34;q11) translocation is found in about 90% of chronic myeloid leukemia (CML) patients. About 5–10% of CML patients have complex variant translocations involving a third chromosome in addition to chromosomes 9 and 22. Herein, we describe a CML-chronic phase male with a complex translocation involving chromosome 16, t(9;22;16)(q34;q11;q24). First, he was treated with interferon-alpha and intermittent hydroxyurea, but only a partial cytogenetic response was attained. Subsequently, the patient was treated with imatinib mesylate because of an additional chromosome abnormality, trisomy 8. A major molecular response was obtained after one year's imatinib therapy, and the follow-up chromosomal analysis performed 4 years and 3 months after the initiation of imatinib therapy displayed a normal karyotype of 46,XY.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom