Clinical Hematology, University Hospital Nancy Brabois, Vandœuvre-lès-Nancy, France.
Blood. 2011 Jul 21;118(3):679-85. doi: 10.1182/blood-2010-09-307264. Epub 2011 May 26.
The prognosis of acute myeloid leukemia (AML) is very poor in elderly patients, especially in those classically defined as having unfavorable cytogenetics. The recent monosomal karyotype (MK) entity, defined as 2 or more autosomal monosomies or combination of 1 monosomy with structural abnormalities, has been reported to be associated with a worse outcome than the traditional complex karyotype (CK). In this retrospective study of 186 AML patients older than 60 years, the prognostic influence of MK was used to further stratify elderly patients with unfavorable cytogenetics. CK was observed in 129 patients (69%), and 110 exhibited abnormalities according to the definition of MK (59%). MK(+) patients had a complete response rate significantly lower than MK(-) patients: 37% vs 64% (P = .0008), and their 2-year overall survival was also decreased at 7% vs 22% (P < .0001). In multivariate analysis, MK appeared as the major independent prognostic factor related to complete remission achievement (odds ratio = 2.3; 95% confidence interval, 1-5.4, P = .05) and survival (hazard ratio = 1.7; 95% confidence interval, 1.1-2.5, P = .008). In the subgroup of 129 CK(+) patients, survival was dramatically decreased for MK(+) patients (8% vs 28% at P = .03). These results demonstrate that MK is a major independent factor of very poor prognosis in elderly AML.
老年急性髓系白血病(AML)患者的预后非常差,尤其是那些经典定义为具有不良细胞遗传学特征的患者。最近,单倍体核型(MK)实体被定义为 2 个或更多常染色体单体缺失或 1 个单体缺失与结构异常的组合,与传统的复杂核型(CK)相比,被报道与更差的预后相关。在这项对 186 名年龄大于 60 岁的 AML 患者的回顾性研究中,MK 的预后影响被用于进一步分层具有不良细胞遗传学特征的老年患者。在 129 名患者(69%)中观察到 CK,110 名患者(59%)根据 MK 的定义表现出异常。MK(+)患者的完全缓解率明显低于 MK(-)患者:37%对 64%(P =.0008),其 2 年总生存率也从 7%下降至 22%(P <.0001)。在多变量分析中,MK 似乎是与完全缓解率相关的主要独立预后因素(优势比=2.3;95%置信区间,1-5.4,P =.05)和生存(风险比=1.7;95%置信区间,1.1-2.5,P =.008)。在 129 名 CK(+)患者亚组中,MK(+)患者的生存明显下降(P =.03)。这些结果表明,MK 是老年 AML 患者预后非常差的主要独立因素。