肿瘤细胞治疗研究
英文原题:Multi-omics-guided dynamic precision medicine in leukemia: An AML-centered framework integrating genotype, cellular state, bone marrow pathology, and the immune ecosystem.
Multi-omics-guided dynamic precision medicine in leukemia: An AML-centered framework integrating genotype, cellular state, bone marrow pathology, and the immune ecosystem.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
白血病是一组以显著分子异质性、细胞状态可塑性和临床结局高度可变性为特征的血液系统恶性肿瘤。随着高通量测序、单细胞与空间组学、分子可测量残留病监测以及免疫工程技术的发展,白血病的诊断与治疗范式正从传统的基于形态学和细胞遗传学的分层,转向由多组学数据驱动的动态精准医学。本文以急性髓系白血病为核心模型,系统整合基因组学、表观基因组学、转录组学、蛋白质组学、代谢组学和空间组学证据,阐明驱动突变、表观遗传调控、白血病干细胞可塑性、克隆演化、骨髓微环境和免疫微环境在疾病分型、风险评估、治疗耐受和复发中的协同作用。关键分子事件,包括 FLT3、NPM1、TP53、IDH1/2、KMT2A 重排和 menin 依赖通路,已显著推进了靶向治疗和风险适应管理。
然而,单一遗传学异常本身不足以完全解释治疗反应和长期预后。相比之下,整合动态 MRD 状态、细胞状态转变、功能性药物脆弱性和免疫生态特征的多维框架,可能更好地识别复发风险、优化治疗顺序,并指导 CAR-T/CAR-NK 治疗、表观遗传治疗和联合免疫治疗策略的个体化应用。尽管多组学数据整合、检测标准化、临床可及性、算法可解释性和前瞻性验证仍是主要挑战,但单细胞与空间组学、AI辅助决策以及数字预测模型有望进一步推动白血病精准医学从静态分型向实时监测、预测建模和适应性干预转变。
总体而言,白血病精准医学的核心目标并非单纯识别更多分子异常,而是将多维生物学信息转化为临床可验证、可操作且可持续优化的决策系统。
Leukemia comprises a group of hematologic malignancies characterized by pronounced molecular heterogeneity, cellular-state plasticity, and highly variable clinical outcomes. With the rapid development of high-throughput sequencing, single-cell and spatial omics, molecular measurable residual disease monitoring, and immune-engineering technologies, the diagnostic and therapeutic paradigm of leukemia is shifting from conventional morphology- and cytogenetics-based stratification toward dynamic precision medicine driven by multi-omics data.
Using acute myeloid leukemia as the core model, this review systematically integrates evidence from genomics, epigenomics, transcriptomics, proteomics, metabolomics, and spatial omics to elucidate the coordinated roles of driver mutations, epigenetic regulation, leukemia stem cell plasticity, clonal evolution, the bone marrow niche, and the immune microenvironment in disease classification, risk assessment, therapeutic tolerance, and relapse.
Key molecular events, including FLT3, NPM1, TP53, IDH1/2, KMT2A rearrangements, and menin-dependent pathways, have substantially advanced targeted therapy and risk-adapted management.
However, single genetic abnormalities alone are insufficient to fully explain treatment response and long-term prognosis. By contrast, a multidimensional framework integrating dynamic MRD status, cellular-state transitions, functional drug vulnerabilities, and immune-ecological features may better identify relapse risk, optimize treatment sequencing, and guide the individualized application of CAR-T/CAR-NK therapy, epigenetic therapy, and combination immunotherapeutic strategies.
Although multi-omics data integration, assay standardization, clinical accessibility, algorithmic interpretability, and prospective validation remain major challenges, single-cell and spatial omics, AI-assisted decision-making, and digital predictive models are expected to further promote the transition of precision medicine in leukemia from static classification to real-time monitoring, predictive modeling, and adaptive intervention.
Overall, the central goal of precision medicine in leukemia is not simply to identify more molecular abnormalities, but to translate multidimensional biological information into a clinically verifiable, actionable, and continuously optimizable decision-making system.
MEMBER ACCOUNT
登录成功会直接打开下一页。