| Literature DB >> 25765803 |
Seiichiro Katagiri1, Tetsuzo Tauchi, Tomohiro Umezu, Yuu Saito, Tamiko Suguro, Michiyo Asano, Seiichiro Yoshizawa, Toshihiko Kitahara, Daigo Akahane, Yuko Tanaka, Hiroaki Fujimoto, Seiichi Okabe, Moritaka Gotoh, Yoshikazu Ito, Junko H Ohyashiki, Kazuma Ohyashiki.
Abstract
A 51-year-old man with chronic myeloid leukemia (CML) was treated with imatinib (IM). After 24 months of treatment, he achieved a complete molecular response (CMR), which he sustained for 3 years. However, 4 months after discontinuing IM treatment, the CML relapsed. The patient was treated again with IM and achieved CMR. A combination of IM and interferon-α (IFNα) was administered for the following year, and then discontinued. The patient has since sustained CMR without therapy for 24 months, to date. This patient was found to have a BCL2L11 (BIM) deletion polymorphism. CML patients with a BIM deletion polymorphism show a low response to IM, and we infer that the BIM deletion polymorphism is a negative factor for discontinuation of IM. IFNα treatment is expected to prevent relapse during immunological surveillance. Therefore, the combination of IM and IFNα might be a feasible approach for CML patients who experience difficulty with IM discontinuation.Entities:
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Year: 2015 PMID: 25765803 DOI: 10.11406/rinketsu.56.216
Source DB: PubMed Journal: Rinsho Ketsueki ISSN: 0485-1439