Appelbaum Frederick R, Gundacker Holly, Head David R, Slovak Marilyn L, Willman Cheryl L, Godwin John E, Anderson Jeanne E, Petersdorf Stephen H
Southwest Oncology Group, Operations Office, 14980 Omicron Dr, San Antonio, TX 78245-3217, USA.
Blood. 2006 May 1;107(9):3481-5. doi: 10.1182/blood-2005-09-3724. Epub 2006 Feb 2.
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.
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。