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Increased likelihood of post-polycythemia vera myelofibrosis in Ph-negative MPN patients with chromosome 12 abnormalities

机译:Ph阴性MPN患者12号染色体异常的真性红细胞增多症后真核纤维化的可能性增加

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摘要

Chromosome 12 (Chr12) abnormalities have been described for individual patients with Philadelphia chromosome-negative myeloproliferative neoplasms (Ph-neg MPN), however the frequency, characteristics, and outcomes of such patients as a whole have not been investigated. We reviewed a database of 1787 consecutive Ph-neg MPN patients seen at our institution and determined that 2% of Ph-neg MPN patients harbored an alteration involving Chr12 by cytogenetic evaluation. Retrospective chart review revealed that patients with Chr12 abnormalities had a higher likelihood of having myelofibrosis (MF) compared to patients without a Chr12 abnormality, and were more likely to have post-polycythemia vera MF. The most common alterations in Chr12 in MF patients involved 12q13, 12q15, 12q24, and trisomy 12, and >40% of Chr12 Ph-neg MPN patients had cytogenetic evolution. Chr12 abnormalities did not significantly correlate with JAK2 status, progression to acute myeloid leukemia, or survival, however patients with 12q24 abnormalities trended towards poorer outcomes.
机译:已经描述了费城染色体阴性骨髓增生性肿瘤(Ph-neg MPN)的个别患者的12号染色体(Chr12)异常,但是总体上尚未研究此类患者的频率,特征和结局。我们回顾了我们机构中连续出现的1787名Ph-neg MPN患者的数据库,并通过细胞遗传学评估确定2%的Ph-neg MPN患者具有涉及Chr12的改变。回顾性图表回顾显示,与Chr12异常患者相比,Chr12异常患者发生骨髓纤维化(MF)的可能性更高,并且真性红细胞增多症也更容易发生。 MF患者中最常见的Chr12改变涉及12q13、12q15、12q24和12三体性,并且Chr12 Ph-neg MPN患者中> 40%具有细胞遗传学进化。 Chr12异常与JAK2的状态,进展为急性髓细胞性白血病或生存没有显着相关,但是12q24异常的患者倾向于转归较差。

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