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费城阴性细胞中的克隆性染色体畸变,如7号染色体单体和8号染色体三体,可能会持续数年,而对慢性髓性白血病患者的长期预后没有影响。

Clonal chromosomal aberrations in Philadelphia negative cells such as monosomy 7 and trisomy 8 may persist for years with no impact on the long term outcome in patients with chronic myeloid leukemia.

作者信息

Wasilewska Ewa M, Panasiuk Barbara, Gniot Michał, Sawicka Anna, Kozłowska Katarzyna, Lewandowski Krzysztof, Kłoczko Janusz, Midro Alina T

机构信息

Department of Hematology, Medical University of Bialystok, 24A Skłodowskiej-Curie Street, 15-276 Białystok, Poland.

Department of Clinical Genetics, Medical University of Bialystok, 13 Waszyngtona Street, 15-089 Białystok, Poland.

出版信息

Cancer Genet. 2017 Oct;216-217:1-9. doi: 10.1016/j.cancergen.2017.04.066. Epub 2017 Apr 28.

Abstract

The appearance of clonal chromosomal aberrations in Philadelphia negative cells (CCA/Ph-) during the treatment of chronic myeloid leukemia (CML) was recently confirmed. Importance of these findings has not been clearly defined. We present data on the time of appearance, persistence, size of the CCA/Ph- clone in terms of drugs used and hematological, cytogenetic and molecular response rates. The focus was on the peripheral blood cytopenias and myelodysplastic changes in the bone marrow microscopic evaluation. In 5 out of 155 (3,2%) CML patients, the persistent presence (up to nine years) of CCA/Ph- was found (monosomy 7 and trisomy 8 in unrelated clones in two patients treated with tyrosine kinase inhibitors; trisomy 8 in two patients on imatinib; trisomy 21 in one patient on interferon alfa treatment). Aberrations were present in median 24% Ph- cells in 3-15 subsequent analyses at different cytogenetic and molecular response time points. No evident myelodysplastic changes nor transformation to MDS/AML occurred in patients with CCA/Ph-. All the patients achieved major molecular response (MMR). It seems that CCA/Ph- presence does not affect the long term outcome in patients with chronic myeloid leukemia. Further complex monitoring of the CML patients with CCA/Ph- is still needed.

摘要

近期已证实,在慢性髓性白血病(CML)治疗期间,费城阴性细胞(CCA/Ph-)中会出现克隆性染色体畸变。这些发现的重要性尚未明确界定。我们根据所用药物以及血液学、细胞遗传学和分子反应率,呈现了CCA/Ph-克隆的出现时间、持续时间和大小的数据。重点关注外周血细胞减少以及骨髓显微镜评估中的骨髓发育异常变化。在155例CML患者中的5例(3.2%)中,发现CCA/Ph-持续存在(长达9年)(2例接受酪氨酸激酶抑制剂治疗的患者中,无关克隆出现7号染色体单体和8号染色体三体;2例接受伊马替尼治疗的患者出现8号染色体三体;1例接受干扰素α治疗的患者出现21号染色体三体)。在不同细胞遗传学和分子反应时间点的3 - 15次后续分析中,畸变存在于中位24%的Ph-细胞中。CCA/Ph-患者未出现明显的骨髓发育异常变化,也未转化为MDS/AML。所有患者均实现了主要分子反应(MMR)。似乎CCA/Ph-的存在并不影响慢性髓性白血病患者的长期预后。仍需要对CCA/Ph-的CML患者进行进一步的综合监测。

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