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

被引:41
|
作者
Khanna, Vishesh [1 ,2 ,3 ]
Pierce, Scott T. [4 ]
Dao, Kim-Hien T. [1 ]
Tognon, Cristina E. [1 ]
Hunt, David E. [5 ]
Junio, Brian [1 ]
Tyner, Jeffrey W. [1 ]
Druker, Brian J. [1 ,6 ,7 ]
机构
[1] Oregon Hlth & Sci Univ, Knight Canc Inst, Portland, OR 97201 USA
[2] Howard Hughes Med Inst, Howard Hughes Med Inst Med Res Fellows Program, Chevy Chase, MD USA
[3] Case Western Reserve Univ, Cleveland Clin, Lerner Coll Med, Cleveland, OH 44106 USA
[4] St Joseph Hosp, Dept Hematol Oncol, Nashua, NH USA
[5] Howard Hughes Med Inst, Howard Hughes Med Inst Investigator Program, Chevy Chase, MD USA
[6] Oregon Hlth & Sci Univ, Div Hematol & Med Oncol, Portland, OR 97201 USA
[7] Oregon Hlth & Sci Univ, Dept Cell Dev & Canc Biol, Portland, OR 97201 USA
来源
CUREUS | 2015年 / 7卷 / 12期
关键词
atypical chronic myeloid leukemia; chronic neutrophilic leukemia; trametinib; nras;
D O I
10.7759/cureus.414
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 welldefined. 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.
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页数:5
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