Cuzick J, Erskine S, Edelman D, Galton D A
Br J Cancer. 1987 May;55(5):523-9. doi: 10.1038/bjc.1987.107.
Twelve of 648 patients in the Medical Research Council's first two trials in myelomatosis have developed myelodysplasia or acute leukaemia. This corresponds to a 5-year actuarial prevalence of 3% and an 8-year prevalence of 10%. Patients were randomised to treatment with either melphalan or cyclophosphamide and the relative capabilities of these two drugs to cause these conditions were examined as a function of duration of treatment. A significant relationship with length of melphalan treatment was found but no relationship was observed for cyclophosphamide treatment. The amount of melphalan treatment given in various intervals before diagnosis of myelodysplasia or leukaemia was studied and it was found that the amount of treatment in the most recent 3-year period was the most important determinant of risk (P = 0.0001). It is estimated that the risk of haemopoietic neoplasia after 10 years of follow-up is about 3% for each year of melphalan treatment and that much of this risk will occur within three years of the last treatment.
医学研究委员会在前两项骨髓瘤试验的648名患者中,有12人发生了骨髓发育异常或急性白血病。这相当于5年精算患病率为3%,8年患病率为10%。患者被随机分配接受美法仑或环磷酰胺治疗,并根据治疗持续时间研究这两种药物导致这些病症的相对能力。发现与美法仑治疗时长存在显著关系,但未观察到与环磷酰胺治疗的关系。研究了在诊断骨髓发育异常或白血病之前不同时间段给予的美法仑治疗量,发现最近3年的治疗量是风险的最重要决定因素(P = 0.0001)。据估计,美法仑治疗每1年,随访10年后发生造血肿瘤的风险约为3%,且这种风险大部分将在最后一次治疗后的3年内出现。