Hsiao Hui-Hua, Sashida Goro, Ito Yoshikazu, Kodama Atsushi, Fukutake Katsuyuki, Ohyashiki Junko H, Ohyashiki Kazuma
The First Department of Internal Medicine; Department of Internal Medicine, Kaohsiung Medical University Hospital, 100, Tz-You 1st Road, Kaohsiung 807, Taiwan.
Cancer Genet Cytogenet. 2006 Mar;165(2):161-6. doi: 10.1016/j.cancergencyto.2005.09.003.
We analyzed 23 patients with myelodysplastic syndromes (MDS) and acute myeloid leukemia (AML) showing a der(1;7)(q10;p10) [hereafter der(1;7)] to identify the exact predictive factor of this cytogenetic change. Eight (34.8%) patients, including six with MDS and two with AML patients, had a previous history of genotoxic exposure, especially radiation and/or antimetabolites. Patients with der(1;7) consisted of three groups: one third of patients had a previous history of genotoxic agents, one third had additional cytogenetic changes at the time of MDS/AML diagnosis without previous exposure history, and the remaining one third had neither a previous exposure history nor additional cytogenetic changes. The current study demonstrated that the poor outcome of MDS/AML with der(1;7) is caused by the high frequency of associated risk factors (i.e., previous history of genotoxic exposure, the presence of additional cytogenetic changes, or both). Identification of prognostic disadvantage might be required for applying the appropriate strategy in managing MDS/AML patients with rare der(1;7) abnormality.
我们分析了23例骨髓增生异常综合征(MDS)和急性髓系白血病(AML)患者,这些患者显示出der(1;7)(q10;p10) [以下简称der(1;7)],以确定这种细胞遗传学改变的确切预测因素。8例(34.8%)患者,包括6例MDS患者和2例AML患者,有既往遗传毒性暴露史,尤其是辐射和/或抗代谢物。有der(1;7)的患者分为三组:三分之一的患者有既往遗传毒性物质暴露史,三分之一的患者在MDS/AML诊断时伴有其他细胞遗传学改变但无既往暴露史,其余三分之一既无既往暴露史也无其他细胞遗传学改变。当前研究表明,伴有der(1;7)的MDS/AML预后不良是由相关危险因素的高频率所致(即既往遗传毒性暴露史、存在其他细胞遗传学改变或两者皆有)。对于管理伴有罕见der(1;7)异常的MDS/AML患者,可能需要识别预后不良因素以应用适当的策略。