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Prognostic significance of SRSF2 mutations in myelodysplastic syndromes and chronic myelomonocytic leukemia: a meta-analysis

机译:SRSF2突变在骨髓增生异常综合症和慢性粒细胞单核细胞白血病中的预后意义:一项荟萃分析

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Objective: Serine/arginine-rich splicing factor 2 (SRSF2) mutations were detected frequently in myelodysplastic syndrome (MDS) and chronic myelomonocytic leukemia (CMML) patients. However, its prognostic value has not yet been fully clarified. Methods: In this meta-analysis, Hazard Ratio (HR) and 95% confidence interval (CI) for overall-survival (OS) were chosen to evaluate the prognostic impact of SRSF2 mutations and to compare SRSF2 mutations to those with wild-type. Results: A total of 2056 patients from 12 studies were obtained. The pooled HRs for OSsuggested that patients with MDS had a poorer prognosis (HR?=?1.780, 95% CI (1.410–2.249)), while analysis on SRSF2 mutations revealed no significant effect on the prognosis of CMML patients (HR?=?1.091, 95% CI (0.925–1.286)). The frequency of SRSF2 mutations was found to be 11.5% and 39.8% in patients with MDS and CMML, respectively. Discussion: This meta-analysis suggests that SRSF2 has a poor prognosis in patients with MDS, but no prognosis impact on patients with CMML. Conclusion: In conclusion, SRSF2 mutations were significantly related to the shorter OS in patients with MDS which may consider as an adverse prognostic risk factor. Whereas, analysis did not show any prognostic effect on OS of CMML patients with SRSF2 mutations.
机译:目的:在骨髓增生异常综合症(MDS)和慢性粒细胞性单核细胞白血病(CMML)患者中经常检测到富含丝氨酸/精氨酸的剪接因子2(SRSF2)突变。但是,其预后价值尚未完全阐明。方法:在这项荟萃分析中,选择整体生存率(OS)的危险比(HR)和95%置信区间(CI)来评估SRSF2突变的预后影响,并将SRSF2突变与野生型进行比较。结果:从12项研究中总共获得2056例患者。 OS汇总的HRs提示MDS患者的预后较差(HR = 1.780,95%CI(1.410-2.249)),而对SRSF2突变的分析显示,对CMML患者的预后没有显着影响(HR ==? 1.091,95%CI(0.925-1.286)。发现MDS和CMML患者的SRSF2突变频率分别为11.5%和39.8%。讨论:这项荟萃分析表明,SRSF2在MDS患者中预后较差,但对CMML患者无预后影响。结论:总之,SRSF2突变与MDS患者较短的OS密切相关,这可能被认为是不良的预后危险因素。鉴于分析未显示对具有SRSF2突变的CMML患者的OS有任何预后影响。

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