急性髓性白血病与年龄有关的动态变化:对预后、风险分层和治疗反应的影响

IF 0.1 Q4 HEMATOLOGY Iraqi Journal of Hematology Pub Date : 2024-03-15 DOI:10.4103/ijh.ijh_7_24
A. Aljabban, J. Alalsaidissa
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引用次数: 0

摘要

急性髓性白血病(AML)是一种由获得性体细胞突变驱动的复杂、异质性疾病。特定突变的存在会促进分层、治疗和预后。随着时间的推移,突变的线性累积是癌症发展的一个关键因素,尤其是在老年患者中。我们最近对急性髓细胞性白血病基因重排的研究显示,年龄与不良风险病例之间存在显著关联。 本研究旨在探讨伊拉克新发急性髓细胞性白血病患者的年龄分布、分子特征、风险分层以及基于年龄的治疗反应。 一项前瞻性队列研究在 2020 年 12 月至 2022 年 5 月期间招募了 115 名使用形态学和流式细胞术诊断为新发急性髓细胞性白血病的伊拉克成年患者。白血病 Q-Fusion 筛查试剂盒采用多重反转录-实时定量聚合酶链反应,可检测 30 个基因重排,用于鉴定基因重排。患者在医疗城巴格达教学医院血液科接受治疗和随访。研究开始前已获得巴格达大学医学院伦理委员会的伦理批准,确保整个研究过程符合伦理标准。 患者的年龄分布呈双峰型,平均年龄为 45.1 ± 17.5 岁,从 18 岁到 84 岁不等,中位数为 46 岁。39.1%的患者在35岁之前被诊断为急性髓细胞性白血病,43%的患者在51岁之后被诊断为急性髓细胞性白血病。RARA基因突变、RUNX1:: RUNX1T1基因改变和NPM1基因突变的急性髓细胞性白血病患者主要见于年轻人,以及诊断为分化型急性髓细胞性白血病的患者。相反,KMT2A重排在年龄较大的人群中更为普遍,根据世界卫生组织(WHO)的急性髓细胞性白血病分类,不同年龄段的分布差异有统计学意义(P = 0.001)。根据年龄和反应评估进行的风险分层显示,老年患者的风险明显较高,这与不良风险、较差的反应和死亡率有关(P < 0.05)。将年龄加入WHO分类和ELN 2022风险分层后,治疗反应预测的准确率有所提高(73.5%-87.9%)。 年龄对急性髓细胞性白血病的预后和治疗反应有重大影响。将年龄纳入风险分层可提高准确性。考虑年龄的定制方法对于优化急性髓细胞白血病的管理和预后至关重要。
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Age-related dynamics in acute myeloid leukemia: Implications for prognosis, risk stratification, and treatment response
Acute myeloid leukemia (AML) is a complex, heterogeneous disease driven by acquired somatic mutations. The presence of specific mutations advances stratification, treatment, and prognosis. Linear accumulation of mutations over time is a crucial factor in cancer development, particularly among elderly patients. Our recent study on gene rearrangement in AML revealed a significant association between age and adverse risk cases. The aim of this study was to examine the distribution of age, molecular characteristics, risk stratification, and treatment response based on age among patients with de novo AML in Iraq. A prospective cohort study enrolled 115 Iraqi adult patients diagnosed with de novo AML using morphology and flow cytometry from December 2020 to May 2022. The Leukemia Q-Fusion Screening Kit, employing multiplex reverse transcription–real-time quantitative polymerase chain reaction with 30 gene rearrangements, was employed for the identification of gene rearrangement. The patients received care and follow-up at the Hematology Unit of Baghdad Teaching Hospital in Medical City. Ethical approval from the College of Medicine’s Ethical Committee at the University of Baghdad was secured before commencing the research, ensuring adherence to ethical standards throughdout the study. The age distribution exhibited a bimodal pattern, with a mean of 45.1 ± 17.5 years, ranging from 18 to 84 years, and a median of 46 years. A total of 39.1% of patients were diagnosed with AML before the age of 35 years, while 43% were diagnosed after the age of 51 years. AML patients with RARA mutations, RUNX1:: RUNX1T1 alterations, and NPM1 mutations were predominantly observed in younger individuals, as well as those diagnosed with AML defined by differentiation. Conversely, KMT2A rearrangements were more prevalent among older age groups, with a statistically significant difference in the distribution of AML classifications according to the World Health Organization (WHO) by age categories (P = 0.001). The risk stratification based on age and response assessment showed a notable higher risk profile observed among elderly patients that was associated with adverse risk and poorer response and mortality (P < 0.05). The prediction of treatment response accuracy rate was improved by adding age to the WHO classification and ELN 2022 risk stratification (73.5%–87.9%). Age significantly influences AML prognosis and treatment response. Incorporating age into risk stratification improves accuracy. Tailored approaches considering age are vital for optimizing AML management and outcomes.
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