Whang-Peng J, Knutsen T, O'Donnell J F, Brereton H D
Cancer. 1979 Nov;44(5):1592-600. doi: 10.1002/1097-0142(197911)44:5<1592::aid-cncr2820440509>3.0.co;2-a.
Seven cases of acute nonlymphocytic leukemia (ANLL) and one of malignant myeloproliferative syndrome were identified from a pool of 189 cases of non-Hodgkin's lymphoma (NHL) and CLL treated primarily with extensive radiotherapy at the Clinical Center, the National Institutes of Health. Four patients also received chemotherapy, two for only short periods. The median time interval from the diagnosis of the primary malignancy to the development of leukemia was 61 months (range 33 to 98 months) and the median survival after the diagnosis of leukemia was two months (0 to 9 months). All eight patients were cytogenetically abnormal and serial chromosome studies revealed that hypodiploidy was the most commonly observed chromosomal abnormality. Abnormalities of chromosome no. 7 were seen in all five patients analyzed by the chromosome banding technique; four of them had monosomy 7. The next most frequently involved chromosome was no. 5. The complexity, extensive nature, and long duration of the cytogenetic abnormalities prior to the diagnosis of leukemia in these patients may be characteristic of secondary leukemia in radiation-treated lymphoma and the presence of such anomalies may predict leukemic transformation.
在美国国立卫生研究院临床中心接受主要以广泛放疗治疗的189例非霍奇金淋巴瘤(NHL)和慢性淋巴细胞白血病(CLL)患者中,确诊了7例急性非淋巴细胞白血病(ANLL)和1例恶性骨髓增殖综合征。4例患者还接受了化疗,其中2例仅短期化疗。从原发性恶性肿瘤诊断到白血病发生的中位时间间隔为61个月(范围33至98个月),白血病诊断后的中位生存期为2个月(0至9个月)。所有8例患者细胞遗传学均异常,连续染色体研究显示亚二倍体是最常见的染色体异常。通过染色体显带技术分析的所有5例患者均可见7号染色体异常;其中4例为7号染色体单体。其次最常受累的染色体是5号染色体。这些患者在白血病诊断前细胞遗传学异常的复杂性、广泛性和持续时间长,可能是放疗后淋巴瘤继发性白血病的特征,此类异常的存在可能预示着白血病转化。