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MEK抑制对NRAS突变的非典型慢性髓性白血病患者的持久疾病控制作用

Durable Disease Control with MEK Inhibition in a Patient with NRAS-mutated Atypical Chronic Myeloid Leukemia.

作者信息

Khanna Vishesh, Pierce Scott T, Dao Kim-Hien T, Tognon Cristina E, Hunt David E, Junio Brian, Tyner Jeffrey W, Druker Brian J

机构信息

Knight Cancer Institute, Oregon Health & Science University ; Howard Hughes Medical Institute Medical Research Fellows Program, Howard Hughes Medical Institute ; Cleveland Clinic Lerner College of Medicine, Case Western Reserve University.

Department of Hematology/Oncology, Saint Joseph Hospital.

出版信息

Cureus. 2015 Dec 17;7(12):e414. doi: 10.7759/cureus.414.

Abstract

Atypical chronic myeloid leukemia (aCML) and chronic neutrophilic leukemia (CNL) are rare hematologic neoplasms characterized by leukocytosis and a hypercellular bone marrow. Although recurrent mutations in the colony-stimulating factor 3 receptor (CSF3R) are frequently observed in patients with (CNL), the mutational landscape in (aCML) is less well-defined. In this report, we describe an 81-year-old male who was diagnosed with aCML. He presented with leukocytosis and anemia but no significant clinical symptoms. Standard laboratory studies revealed the absence of the Philadelphia chromosome. Massively parallel sequencing demonstrated no mutations in CSF3R, but the presence of a heterozygous NRAS-G12D variant (47% allele frequency). The patient was started on treatment with trametinib, an MEK1/2 inhibitor with Food and Drug Administration approval for malignant melanoma. Therapy with trametinib resulted in exceptional improvements in his blood counts and continued disease control with 14 months of follow-up. This case highlights the need for clinical trials evaluating the safety and efficacy of MEK1/2 as a therapeutic target for the treatment of patients with NRAS-mutated aCML/CNL.

摘要

非典型慢性髓性白血病(aCML)和慢性中性粒细胞白血病(CNL)是罕见的血液系统肿瘤,其特征为白细胞增多和骨髓细胞过多。虽然在慢性中性粒细胞白血病(CNL)患者中经常观察到集落刺激因子3受体(CSF3R)的复发性突变,但非典型慢性髓性白血病(aCML)中的突变情况尚不明确。在本报告中,我们描述了一名81岁被诊断为非典型慢性髓性白血病(aCML)的男性。他表现为白细胞增多和贫血,但无明显临床症状。标准实验室检查显示无费城染色体。大规模平行测序显示集落刺激因子3受体(CSF3R)无突变,但存在杂合NRAS - G12D变异(等位基因频率为47%)。该患者开始接受曲美替尼治疗,曲美替尼是一种经美国食品药品监督管理局批准用于治疗恶性黑色素瘤的MEK1/2抑制剂。曲美替尼治疗使他的血细胞计数有显著改善,并在14个月的随访中持续控制疾病。该病例强调了开展临床试验以评估MEK1/2作为NRAS突变的非典型慢性髓性白血病/慢性中性粒细胞白血病(aCML/CNL)患者治疗靶点安全性和有效性的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16bf/4725740/972c672030a5/cureus-0007-000000000414-i01.jpg

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