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鲁索替尼(Ruxolitinib)加地西他滨(Decitabine)通过降低 KRAS 的变异等位基因频率,有效治疗无法分类的骨髓增生异常综合征/骨髓增生性肿瘤
Authors Luo S, Xu X, Ye X, Zhu X, Wu C, Chen D, Jin J, Zheng Y, Zheng M, Huang J
Received 15 July 2020
Accepted for publication 15 September 2020
Published 9 October 2020 Volume 2020:13 Pages 10143—10148
DOI https://doi.org/10.2147/OTT.S272207
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 3
Editor who approved publication: Dr Arseniy Yuzhalin
Abstract: Myelodysplastic syndrome/myeloproliferative neoplasm, unclassifiable (MDS/MPN-U) is a subtype of MDS/MPN that exhibits a combination of the features of both MDS and MPN. To date, no curative treatment is available for MDS/MPN-U; however, previous studies have suggested a potential survival advantage for ruxolitinib and hypomethylating agents. We reported a case of a JAK2 -negative but KRAS -positive MDS/MPN-U patient treated with ruxolitinib plus decitabine. After treatment, the patient’s clinical symptoms were moderated, and the size of the spleen and the peripheral blood cell counts were reduced. These effects might be due to the regimen’s ability to reduce STAT5 activation and upregulate microRNA-181c to downregulate the variant allele frequency (VAF) of KRAS .
Keywords: myelodysplastic syndrome, myeloproliferative neoplasm, decitabine, ruxolitinib, KRAS
