基因检测时代骨髓增生异常综合征的诊断与治疗

Junshik Hong
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摘要

骨髓增生异常综合征(MDS)是一种异质性疾病,其预后受细胞减少症、基因变异和骨髓中骨髓细胞比例的影响而各不相同。准确的预后预测和量身定制的治疗方案至关重要。国际预后评分系统-分子(IPSS-M)除了反映临床和实验室信息外,还反映了 MDS 相关基因突变的影响,与现有系统(如修订版国际预后评分系统(IPSS-R))相比,有望提供更高的预后准确性。尽管该系统在统计上较为复杂,但其基于网络的计算方法以及利用直观数据集与患者讨论结果的便利性却具有显著优势。SF3B1 基因突变病例中使用红细胞生成饱和剂有效纠正贫血,TP53 基因突变病例中努力改善不良预后,这些都是 MDS 治疗取得进展的例证,反映了基于基因的 MDS 干预方法在不断发展。基因诊断技术的进步,加上对骨髓生态位的进一步了解,预计将在未来显著改善 MDS 的治疗效果。
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Diagnosis and Treatment of Myelodysplastic Syndrome in the Era of Genetic Testing
Myelodysplastic syndrome (MDS) is a heterogeneous disorder with diverse prognoses influenced by cytopenias, genetic variants, and myeloblast proportions in the bone marrow. Accurate prognosis prediction and tailored treatment plans are essential. The International Prognostic Scoring System-Molecular (IPSS-M), which additionally reflects the impact of MDS-related genetic mutations to the clinical and laboratory information, is anticipated to offer superior prognostic accuracy compared to existing systems like the Revised International Prognostic Scoring System (IPSS-R). Despite its statistical complexity, its web-based calculation and ease of discussing results with patients using intuitive data sets provide notable advantages. Progress in MDS treatment, exemplified by effective anemia correction with an erythropoiesis-maturation agent in SF3B1-mutated cases and efforts to refine poor prognoses in TP53-mutated cases, reflects the evolving landscape of genetic-based interventions in MDS. Advancements in genetic diagnostic technology, combined with enhanced knowledge of the bone marrow niche, are anticipated to lead to significant improvement in MDS treatment outcomes in the future.
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