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

被引:35
作者
Jafari, Pourya Arbab [1 ]
Ayatollahi, Hossein [1 ]
Sadeghi, Ramin [2 ]
Sheikhi, Maryam [3 ]
Asghari, Amir [4 ]
机构
[1] Mashhad Univ Med Sci, Fac Med, Dept Hematol & Blood Banking, Mashhad, Iran
[2] Mashhad Univ Med Sci, Fac Med, Dept Nucl Med, Mashhad, Iran
[3] Mashhad Univ Med Sci, Canc Mol Pathol Res Ctr, Fac Med, Mashhad, Iran
[4] Mashhad Univ Med Sci, Dept Physiol, Fac Med, Mashhad, Iran
关键词
Myelodysplastic syndrome; SRSF2; mutation; prognosis; meta-analysis; GENETIC-BASIS; MACHINERY; PATHWAY; U2AF1; SF3B1;
D O I
10.1080/10245332.2018.1471794
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:778 / 784
页数:7
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