Literature DB >> 25765803

[Treatment-free molecular remission achieved by combination therapy with imatinib and IFNα in CML with BIM deletion polymorphism relapsed after stop imatinib].

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.

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Year:  2015        PMID: 25765803     DOI: 10.11406/rinketsu.56.216

Source DB:  PubMed          Journal:  Rinsho Ketsueki        ISSN: 0485-1439


  1 in total

1.  Effects of a Particular Heptapeptide on the IFN-α-Sensitive CML Cells.

Authors:  Fu-Lan Yang; Fang-Zhi Chen; Xin-Xing Wan; Xi Zhou; Mei-Juan Zhou; Han-Chun Chen; Jun-Jiang Fu; Dian-Zheng Zhang
Journal:  Biomed Res Int       Date:  2015-09-01       Impact factor: 3.411

  1 in total

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