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

被引:2
|
作者
Lee, Yen-Chien [1 ,2 ]
Hsieh, Chung-Cheng [3 ]
Lee, Yen-Ling [1 ]
Li, Chung-Yi [4 ,5 ]
机构
[1] Tainan Hosp, Minist Hlth & Welf, Dept Oncol, Tainan, Taiwan
[2] Natl Cheng Kung Univ, Dept Internal Med, Tainan, Taiwan
[3] Univ Massachusetts, Med Sch, Dept Mol Cell & Canc Biol, Worcester, MA 01605 USA
[4] Natl Cheng Kung Univ, Coll Med, Dept Publ Hlth, Tainan, Taiwan
[5] China Med Univ, Coll Publ Hlth, Dept Publ Hlth, Taichung, Taiwan
来源
CLINICAL LYMPHOMA MYELOMA & LEUKEMIA | 2018年 / 18卷 / 09期
关键词
Leukemia-free survival; Meta-analysis; Molecular markers; Myelofibrosis; Overall survival; JAK2V617F ALLELE BURDEN; STEM-CELL TRANSPLANTATION; MYELOPROLIFERATIVE NEOPLASMS; MUTATIONAL STATUS; JAK2; V617F; POLYCYTHEMIA-VERA; CALR MUTATIONS; SURVIVAL; MPL; TRANSFORMATION;
D O I
10.1016/j.clml.2018.06.004
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:558 / 568
页数:11
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