Einhorn N, Eklund G, Franzén S, Lambert B, Lindsten J, Söderhäll S
Cancer. 1982 Jun 1;49(11):2234-41. doi: 10.1002/1097-0142(19820601)49:11<2234::aid-cncr2820491106>3.0.co;2-q.
Late side effects of chemotherapy were studied in 51 women who had received at least 300 mg of melphalan for ovarian cancer and had survived for at least three years. Hematologic, statistical, and cytogenetic methods were employed. Six cases of iatrogenic leukemia were found. They appeared to represent a hematologic entity that is fairly difficult to recognize. The risk of iatrogenic leukemia in women who survived for three years or more after melphalan treatment was calculated to be 950 times greater than the leukemia risk in the total female population. The cytogenetic changes were studied with three methods focused on sister chromatid exchange, chromosome aberrations, and DNA damage. The sister chromatid exchange frequency showed a marked increase, but it was corrected within a few months. Chromosome aberrations expressed by chromosome rearrangements were increased in the peripheral lymphocytes and may persist for several years. The frequency of DNA stand breaks was decreased indicating the presence of DNA cross-links. Any of these types of genetic alteration could be the initiating event in carcinogenesis.
对51名因卵巢癌接受至少300毫克美法仑治疗且存活至少三年的女性进行了化疗晚期副作用的研究。采用了血液学、统计学和细胞遗传学方法。发现6例医源性白血病病例。它们似乎代表了一种相当难以识别的血液学实体。美法仑治疗后存活三年或更长时间的女性发生医源性白血病的风险经计算比全体女性人群的白血病风险高950倍。采用三种方法研究细胞遗传学变化,重点是姐妹染色单体交换、染色体畸变和DNA损伤。姐妹染色单体交换频率显著增加,但在几个月内得到纠正。外周淋巴细胞中由染色体重排表示的染色体畸变增加,且可能持续数年。DNA链断裂频率降低,表明存在DNA交联。这些类型的基因改变中的任何一种都可能是致癌作用的起始事件。