Department of Hematology and Oncology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya 466-8550, Japan.
Int J Hematol. 2010 Nov;92(4):664-6. doi: 10.1007/s12185-010-0706-6. Epub 2010 Oct 22.
T315I mutation of the ABL-kinase domain in chronic myeloid leukemia (CML) confers resistance to imatinib (IM) as well as second-generation tyrosine kinase inhibitors (TKIs). We report a chronic-phase CML patient undergoing IM treatment, who showed the overt existence of the T315I mutation after 15 months. We retrospectively analyzed the distribution of the T315I mutation using the invader assay and direct DNA sequencing among FACSAria-sorted populations from bone marrow cells: total mononuclear cells (TMC), hematopoietic stem cells (HSC)/Thy-1(+), HSC/Thy-1⁻, common myeloid progenitors (CMP), granulocyte macrophage progenitors (GMP), and megakaryocyte erythroid progenitors (MEP), at 0, 3, 6, 9, and 12 months after IM treatment. T315I was barely detectable by 12 months in TMC, but detectable in 19.2% of HSC/Thy-1⁻ and 46.4% of MEP at diagnosis, and finally expanded into all populations. These results suggest that the monitoring of gene mutations in HSC and progenitors at diagnosis might be helpful for the early detection of TKI-resistant CML patients and facilitate appropriate therapeutic decision.
T315I 突变的 ABL-激酶结构域在慢性髓性白血病 (CML) 中导致对伊马替尼 (IM) 以及第二代酪氨酸激酶抑制剂 (TKI) 的耐药性。我们报告了一位接受 IM 治疗的慢性期 CML 患者,在 15 个月后出现明显的 T315I 突变。我们通过入侵检测和直接 DNA 测序,对骨髓细胞中来自 FACSAria 分选的群体中的 T315I 突变分布进行了回顾性分析:总单核细胞 (TMC)、造血干细胞 (HSC)/Thy-1(+)、HSC/Thy-1⁻、共同髓系祖细胞 (CMP)、粒细胞-巨噬细胞祖细胞 (GMP)和巨核细胞-红细胞祖细胞 (MEP),在 IM 治疗后 0、3、6、9 和 12 个月。12 个月时 TMC 中几乎检测不到 T315I,但在诊断时可检测到 19.2%的 HSC/Thy-1⁻和 46.4%的 MEP,最终扩展到所有群体。这些结果表明,在诊断时对 HSC 和祖细胞中的基因突变进行监测可能有助于早期发现 TKI 耐药性 CML 患者,并有助于做出适当的治疗决策。