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慢性髓性白血病患者酪氨酸激酶抑制剂治疗后达到主要分子学缓解,继而发生伴有 IDH2 和 NPM1 突变的费城染色体阴性急性髓系白血病。

Development of Philadelphia chromosome-negative acute myeloid leukemia with IDH2 and NPM1 mutations in a patient with chronic myeloid leukemia who showed a major molecular response to tyrosine kinase inhibitor therapy.

机构信息

Department of Hematology and Oncology, Dokkyo Medical University, 880 Kitakobayashi, Mibu-machi, Shimotsuga-gun, Tochigi, 321-0293, Japan.

Department of Pathology and Tumor Biology, Kyoto University, Kyoto, Japan.

出版信息

Int J Hematol. 2021 Jun;113(6):936-940. doi: 10.1007/s12185-020-03074-7. Epub 2021 Jan 5.

Abstract

Tyrosine kinase inhibitors (TKIs) are standard therapies for chronic myeloid leukemia (CML) that can eradicate Ph-positive leukemic cells. However, disease control is not achievable in a minority of cases, most commonly due to evolution of TKI-resistant clones. There have also been rare cases of emergence of Ph-negative clones with other cytogenetic abnormalities, and, less commonly, development of Ph-negative acute myeloid leukemia (AML), whose molecular pathogenesis is largely unknown. Here we report molecular features of a patient with Ph + CML who developed Ph-negative AML after showing a major molecular response to dasatinib. A 55-year-old man was diagnosed with CML. He achieved a complete cytogenetic response three months after dasatinib therapy but developed AML with normal karyotype 1 year later. After receiving induction and consolidation chemotherapy for AML, the patient achieved complete remission with no evidence of CML under maintenance with bosutinib. Targeted sequencing of serial bone marrow samples identified mutations in IDH2 and NPM1 in the Ph-negative AML cells, which had not been detected in CML cells. These results suggest that Ph-negative AML in this patient originated from a preleukemic population, which might have expanded during or after the successful elimination of CML clones with TKI therapy.

摘要

酪氨酸激酶抑制剂 (TKI) 是治疗慢性髓性白血病 (CML) 的标准疗法,可消除 Ph 阳性白血病细胞。然而,在少数情况下无法控制疾病,最常见的原因是 TKI 耐药克隆的演变。也有少数 Ph 阴性克隆伴有其他细胞遗传学异常的病例,以及不太常见的 Ph 阴性急性髓系白血病 (AML) 的病例,其分子发病机制尚不清楚。这里我们报告了一名 Ph+CML 患者的分子特征,该患者在对达沙替尼表现出主要分子反应后发展为 Ph 阴性 AML。一名 55 岁男性被诊断为 CML。他在达沙替尼治疗三个月后达到完全细胞遗传学缓解,但一年后出现正常核型的 AML。在接受 AML 的诱导和巩固化疗后,患者在接受 bosutinib 维持治疗时完全缓解,无 CML 证据。对系列骨髓样本的靶向测序在 Ph 阴性 AML 细胞中发现了 IDH2 和 NPM1 的突变,而在 CML 细胞中未检测到这些突变。这些结果表明,该患者的 Ph 阴性 AML 起源于 Preleukemic 人群,可能在 TKI 治疗成功消除 CML 克隆期间或之后扩增。

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