Arthur D C, Bloomfield C D
Cancer Genet Cytogenet. 1984 Jul;12(3):189-99. doi: 10.1016/0165-4608(84)90030-x.
We have analyzed G-banded metaphase chromosomes from 20 patients with treatment-associated acute nonlymphocytic leukemia (t-ANLL). Nine patients were previously treated for hematologic malignancies and 11 for solid tumors. The interval from initial therapy to t-ANLL ranged from 35 to 182 mo (median 75.5 mo). Medial age at diagnosis of t-ANLL was 58.5 years. Clonal chromosome abnormalities were found in 19 patients (95%). Loss or partial deletion of the long arm of chromosomes #5 and/or #7 were most common, occurring in nine patients. These abnormalities were associated with hypodiploid complex karyotypes. Other nonrandom abnormalities recurring among karyotypes with abnormalities of chromosome #5 included loss of one #18, partial deletion of the long arm of chromosome #2, ring chromosomes, and a Philadelphia (Ph1) chromosome. We also identified a group of five patients whose only karyotypic abnormality was addition of whole chromosomes. The remaining five patients had other karyotypic abnormalities, the most common of which were structural rearrangements in a pseudodiploid clone. Combined data from our study and the three previously published large series of patients with t-ANLL studied with banding suggest a relationship between karyotype and intensity of prior therapy, with abnormalities of chromosomes #5 and #7 occurring more often in the intensively treated patients.
我们分析了20例治疗相关急性非淋巴细胞白血病(t-ANLL)患者的G显带中期染色体。9例患者既往接受过血液系统恶性肿瘤治疗,11例接受过实体瘤治疗。从初始治疗到发生t-ANLL的时间间隔为35至182个月(中位时间75.5个月)。t-ANLL诊断时的中位年龄为58.5岁。19例患者(95%)发现有克隆性染色体异常。5号和/或7号染色体长臂的缺失或部分缺失最为常见,9例患者出现此类情况。这些异常与亚二倍体复杂核型有关。在5号染色体异常的核型中反复出现的其他非随机异常包括18号染色体单体、2号染色体长臂部分缺失、环形染色体和费城(Ph1)染色体。我们还发现一组5例患者,其唯一的核型异常是整条染色体的增加。其余5例患者有其他核型异常,最常见的是假二倍体克隆中的结构重排。我们的研究数据与之前发表的3个用显带技术研究t-ANLL患者的大型系列数据综合分析表明,核型与既往治疗强度之间存在关联,5号和7号染色体异常在接受强化治疗的患者中更常见。