Molecular Markers and Prognosis of Myelofibrosis in the Genomic Era: A Meta-analysis

Clin Lymphoma Myeloma Leuk. 2018 Sep;18(9):558-568. doi: 10.1016/j.clml.2018.06.004. Epub 2018 Jun 8.

Abstract

Molecular markers are important in guiding treatment and predicting outcome in the genomic era. Meta-analysis of molecular markers in myelofibrosis through a search of PubMed and Medline through October 31, 2017 was performed. Markers with more than 3 studies that compared overall survival (OS) and leukemia-free survival (LFS) were analyzed. A total of 16 studies were included. Hazard ratios (HRs) for OS were as follows: IDH 2.65 (95% confidence interval [CI], 1.66-4.21), SRSF2 2.12 (95% CI, 1.18-3.79), high-risk myeloma 2.11 (95% CI, 1.70-2.61), ASXL1 1.92 (95% CI, 1.60-2.32), EZH2 1.88 (95% CI, 1.32-2.67), JAK2 1.41 (95% CI, 1.04-1.93) in the univariate analysis and 1.49 (95% CI, 0.42-5.30) in the multivariate analysis. LFS of JAK2 and SRSF2 had HRs of 1.81 (95% CI, 0.42-5.30) and 0.36 (95% CI, 0.02-6.48), respectively. In conclusion, mutations in IDH, SRSF2, and ASXL1 had worse prognosis in OS with HRs around 2. JAK2 and SRSF2 mutation were not associated with increased leukemia transformation. The adverse effect of triple-negative, which was often compared with CALR mutation, needs to be explored.

Keywords: Leukemia-free survival; Meta-analysis; Molecular markers; Myelofibrosis; Overall survival.

Publication types

  • Meta-Analysis
  • Review

MeSH terms

  • Biomarkers / analysis*
  • Genomics / methods*
  • Humans
  • Mutation*
  • Primary Myelofibrosis / genetics
  • Primary Myelofibrosis / pathology*
  • Primary Myelofibrosis / therapy
  • Prognosis

Substances

  • Biomarkers