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本文引用的文献

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The influence of age on prognosis of de novo acute myeloid leukemia differs according to cytogenetic subgroups.年龄对初发急性髓系白血病预后的影响因细胞遗传学亚组而异。
Haematologica. 2004 Sep;89(9):1082-90.
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Age-related epigenetic changes and the immune system.与年龄相关的表观遗传变化与免疫系统。
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Assessment of differences in patient populations selected for excluded from participation in clinical phase III acute myelogenous leukemia trials.对被选入排除参与III期急性髓性白血病临床试验的患者群体差异的评估。
J Clin Oncol. 2003 Nov 1;21(21):3933-9. doi: 10.1200/JCO.2003.03.186.
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An age-induced switch to a hyper-recombinational state.年龄诱导的向高重组状态的转变。
Science. 2003 Sep 26;301(5641):1908-11. doi: 10.1126/science.1087706.
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Outcome after induction chemotherapy for older patients with acute myeloid leukemia is not improved with mitoxantrone and etoposide compared to cytarabine and daunorubicin: a Southwest Oncology Group study.与阿糖胞苷和柔红霉素相比,米托蒽醌和依托泊苷用于老年急性髓系白血病患者诱导化疗后的疗效并无改善:一项西南肿瘤协作组的研究。
Blood. 2002 Dec 1;100(12):3869-76. doi: 10.1182/blood-2001-12-0354. Epub 2002 Aug 1.
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Dependence of age-specific incidence of acute myeloid leukemia on karyotype.急性髓系白血病的年龄别发病率与核型的相关性。
Blood. 2001 Dec 1;98(12):3500. doi: 10.1182/blood.v98.12.3500.
7
The predictive value of hierarchical cytogenetic classification in older adults with acute myeloid leukemia (AML): analysis of 1065 patients entered into the United Kingdom Medical Research Council AML11 trial.老年急性髓系白血病(AML)患者中细胞遗传学分层分类的预测价值:对纳入英国医学研究委员会AML11试验的1065例患者的分析
Blood. 2001 Sep 1;98(5):1312-20. doi: 10.1182/blood.v98.5.1312.
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Attempts to improve treatment outcomes in acute myeloid leukemia (AML) in older patients: the results of the United Kingdom Medical Research Council AML11 trial.改善老年急性髓系白血病(AML)患者治疗效果的尝试:英国医学研究委员会AML11试验的结果
Blood. 2001 Sep 1;98(5):1302-11. doi: 10.1182/blood.v98.5.1302.
9
Karyotype and age in acute myeloid leukemia. Are they linked?急性髓系白血病中的核型与年龄。它们有关联吗?
Cancer Genet Cytogenet. 2001 Apr 15;126(2):155-61. doi: 10.1016/s0165-4608(00)00414-3.
10
Mutations with loss of heterozygosity of p53 are common in therapy-related myelodysplasia and acute myeloid leukemia after exposure to alkylating agents and significantly associated with deletion or loss of 5q, a complex karyotype, and a poor prognosis.p53杂合性缺失的突变在接触烷化剂后的治疗相关骨髓增生异常综合征和急性髓系白血病中很常见,并且与5q缺失或丢失、复杂核型以及不良预后显著相关。
J Clin Oncol. 2001 Mar 1;19(5):1405-13. doi: 10.1200/JCO.2001.19.5.1405.

年龄与急性髓系白血病

Age and acute myeloid leukemia.

作者信息

Appelbaum Frederick R, Gundacker Holly, Head David R, Slovak Marilyn L, Willman Cheryl L, Godwin John E, Anderson Jeanne E, Petersdorf Stephen H

机构信息

Southwest Oncology Group, Operations Office, 14980 Omicron Dr, San Antonio, TX 78245-3217, USA.

出版信息

Blood. 2006 May 1;107(9):3481-5. doi: 10.1182/blood-2005-09-3724. Epub 2006 Feb 2.

DOI:10.1182/blood-2005-09-3724
PMID:16455952
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1895766/
Abstract

We conducted a retrospective analysis of 968 adults with acute myeloid leukemia (AML) on 5 recent Southwest Oncology Group trials to understand how the nature of AML changes with age. Older study patients with AML presented with poorer performance status, lower white blood cell counts, and a lower percentage of marrow blasts. Multidrug resistance was found in 33% of AMLs in patients younger than age 56 compared with 57% in patients older than 75. The percentage of patients with favorable cytogenetics dropped from 17% in those younger than age 56 to 4% in those older than 75. In contrast, the proportion of patients with unfavorable cytogenetics increased from 35% in those younger than age 56 to 51% in patients older than 75. Particularly striking were the increases in abnormalities of chromosomes 5, 7, and 17 among the elderly. The increased incidence of unfavorable cytogenetics contributed to their poorer outcome, and, within each cytogenetic risk group, treatment outcome deteriorated markedly with age. Finally, the combination of a poor performance status and advanced age identified a group of patients with a very high likelihood of dying within 30 days of initiating induction therapy. The distinct biology and clinical responses seen argue for age-specific assessments when evaluating therapies for AML.

摘要

我们对最近西南肿瘤协作组的5项试验中的968例急性髓系白血病(AML)成年患者进行了回顾性分析,以了解AML的特征如何随年龄变化。年龄较大的AML研究患者表现出较差的体能状态、较低的白细胞计数和较低的骨髓原始细胞百分比。56岁以下患者中33%的AML存在多药耐药,而75岁以上患者中这一比例为57%。细胞遗传学预后良好的患者比例从56岁以下者的17%降至75岁以上者的4%。相反,细胞遗传学预后不良的患者比例从56岁以下者的35%增至75岁以上患者的51%。特别显著的是老年人中5号、7号和17号染色体异常的增加。细胞遗传学预后不良的发生率增加导致了他们较差的预后,并且在每个细胞遗传学风险组中,治疗结果随年龄显著恶化。最后,体能状态差和高龄相结合确定了一组在诱导治疗开始后30天内死亡可能性非常高的患者。所观察到的不同生物学特性和临床反应表明,在评估AML治疗方法时应进行年龄特异性评估。