Department of Hematology and Blood Banking, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Department of Hematology and Blood Banking, cancer Molecular Pathology Research Center, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Crit Rev Oncol Hematol. 2020 Jan;145:102832. doi: 10.1016/j.critrevonc.2019.102832. Epub 2019 Nov 15.
Splicing factor 3B subunit 1 (SF3B1) is a complex takes part in intron splicing of pre-mRNA and mutations within it have been reported frequently in myeloid malignancies including myelodysplastic syndromes (MDS). However, its prognostic value has been controversial. Hence, we aimed this meta-analysis to investigate the prognostic effect of SF3B1 mutations in patients with MDS. Several electronic databases were searched in of EMBASE, PubMed, the Cochrane Library and Web of Science (published up to November 2017) to obtain eligible studies. The pooled Hazard Ratio (HRs) and 95% confidence interval (CI) for overall survival (OS) and leukemia-free survival (LFS) as the primary and secondary endpoint, respectively, were chosen and extracted to determine the prognostic impact of SF3B1 mutations and to compare SF3B1 mutations to those with wild-type. Nine cohort studies with a total of 2259 patients were obtained, and the pooled HRs for OS was 0.93 (95% CI: 0.56-1.52, p-value = 0.78) and revealed no significant effect on overall survival of MDS patients by random effect models. Our meta-analysis suggested that SF3B1 has no impact on OS of patients with MDS, however, an adequately designed prospective study with a large number of patients with different type of SF3B1 mutations is needed to confirm these results. Additionally, Begg's and Egger's tests did not show any publication bias.
剪接因子 3B 亚基 1(SF3B1)是一种复合物,参与前体 mRNA 的内含子剪接,其突变已在包括骨髓增生异常综合征(MDS)在内的髓系恶性肿瘤中频繁报道。然而,其预后价值一直存在争议。因此,我们旨在进行这项荟萃分析,以研究 SF3B1 突变对 MDS 患者的预后影响。我们检索了 EMBASE、PubMed、Cochrane 图书馆和 Web of Science 等多个电子数据库(截至 2017 年 11 月发布),以获取合格的研究。选择并提取了总体生存(OS)和无白血病生存(LFS)的合并危险比(HRs)和 95%置信区间(CI)作为主要和次要终点,以确定 SF3B1 突变的预后影响,并将 SF3B1 突变与野生型进行比较。共获得了 9 项队列研究,总计 2259 例患者,OS 的合并 HR 为 0.93(95%CI:0.56-1.52,p 值=0.78),并且通过随机效应模型未发现 SF3B1 突变对 MDS 患者总体生存有显著影响。我们的荟萃分析表明,SF3B1 对 MDS 患者的 OS 没有影响,然而,需要一项设计合理、有大量不同类型 SF3B1 突变患者的前瞻性研究来证实这些结果。此外,Begg 和 Egger 检验未显示任何发表偏倚。