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  4. Prognostic implications of genetic and transcriptomic abnormalities in MDS according to IPSS-R, IPSS-M, and the International Consensus Classification.
 
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Prognostic implications of genetic and transcriptomic abnormalities in MDS according to IPSS-R, IPSS-M, and the International Consensus Classification.

Journal
Blood Cancer Journal
Journal Volume
16
Journal Issue
1
Start Page
Article Number :34
ISSN
2044-5385
Date Issued
2026-03-12
Author(s)
WAN-HSUAN LEE  
HSIN-AN HOU  
Lo, Min-Yen
FENG-MING TIEN  
Xavier Cheng-Hong Tsai  
CHIEN-CHIN LIN  
Chang, Yu-Sung
Peng, Yen-Ling
Tseng, Mei-Hsuan
Kuo, Yuan-Yeh
SHAN-CHI YU  
Liu, Ming-Chih
CHI-YUAN YAO  
CHANG-TSU YUAN  
MING YAO  
CHIA-LANG HSU  
HWEI-FANG TIEN  
BOR-SHENG KO  
WEN-CHIEN CHOU  
DOI
10.1038/s41408-026-01456-4
URI
https://scholars.lib.ntu.edu.tw/handle/123456789/737421
Abstract
Cytogenetic abnormalities and recurrent gene mutations are central to the biology and prognosis of myelodysplastic syndromes/neoplasms (MDS); however, the significance of patients without detectable genomic lesions remains unclear. In this retrospective analysis of 758 patients with primary MDS, the participants were stratified according to the presence of gene mutations and/or cytogenetic abnormalities. Approximately twenty percent lacked both abnormalities and were characterized by younger age, female predominance, lower IPSS-R/IPSS-M risk, and the most favorable survival outcomes. Bulk RNA sequencing further revealed that mutation-negative/normal-karyotype MDS was characterized by immune-metabolic transcriptional programs, whereas genomically altered disease exhibited inflammatory, proliferative, and stress-response signatures, indicating a biologically distinct low-risk state. Therefore, patients without genomic abnormalities appear to constitute a biologically distinct subgroup of MDS. To refine risk assessment beyond IPSS-M systems, a multivariable Cox-based nomogram was developed incorporating age, ferritin level >800 ng/mL, lactate dehydrogenase level >200 U/L, bone marrow fibrosis, and IPSS-M. The proposed model outperformed IPSS-M alone and remained robust following bootstrap validation, allowing individualized 12- and 36-month survival estimation. These findings underscore the limitations of relying solely on molecular assays for risk stratification and support the integration of clinical, genomic, and model-based predictors to improve classification and guide individualized MDS management.
Publisher
Springer Nature
Type
journal article

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