骨髓增生异常综合症
国际预后积分系统
医学
肿瘤科
髓系白血病
内科学
7号染色体(人类)
染色体
队列
细胞遗传学
总体生存率
预测模型
髓样
基因
贫血
染色体异常
白血病
生存分析
判别式
生物信息学
来那度胺
血液学
预后变量
阿扎胞苷
队列研究
多元分析
比例危险模型
回顾性队列研究
作者
María Julia Montoro,Vı́ctor Navarro,Pamela Acha,Claudia Haferlach,Onyee Chan,Yasuo Kubota,Felicitas Schulz,Robert Briski,Najla Al-Ali,Blanca Xicoy,Felix Lopez-Cadenas,Francesc Bosch,Anna Aguilera,Manja Meggendorfer,Lea Naomi Eder,Andrés Jérez,Y C Wang,Alessia Campagna,Luca Lanino,Beate Betz
标识
DOI:10.1182/bloodadvances.2026020633
摘要
Myelodysplastic syndromes with isolated deletion of chromosome 5q [MDS-del(5q)] constitute a distinct biological entity traditionally associated with favorable outcomes, although up to one quarter of patients progress to acute myeloid leukemia (AML). Existing prognostic models, developed in heterogeneous MDS populations, may not adequately capture risk within this subgroup. We assembled an international cohort of 682 patients with MDS-del(5q) to evaluate the performance of the IPSS-R and IPSS-M, identify prognostic variables, and develop a disease-specific prognostic tool, the IPSS-del(5q). Most patients were classified as lower-risk by IPSS-R (94.4%) and IPSS-M (85.5%), yet both systems showed limited discriminatory ability (C-indices ≈0.5). Independent adverse prognostic factors included age ≥70 years, male sex, anemia (hemoglobin ≤10 g/dL), thrombocytopenia (platelets ≤100×10⁹/L), the presence of one additional chromosomal abnormality, ≥2 gene mutations, SF3B1 mutations, and high-risk TP53 status. Six variables were included in the IPSS-del(5q), stratifying patients into standard-risk (74.3%) and high-risk (25.7%) groups with significantly different LFS (69.2 vs. 32.0 months; p<0.01). Moreover, this model reclassified 19.1% of lower-risk IPSS-R and 14.6% of lower-risk IPSS-M patients into the high-risk IPSS-del(5q) group. However, its discriminative power remained modest, with a C-index of 0.60. Overall, this study provides the most comprehensive prognostic evaluation of MDS-del(5q) to date, demonstrates the limited discriminatory capacity of existing MDS scores in this entity, and underscores the need to develop refined disease-specific prognostic approaches for this MDS subtype.