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Secondary myelodysplastic syndrome/acute myeloid leukaemia following mitoxantrone-based therapy for breast carcinoma

机译:基于米托蒽醌治疗的乳腺癌继发性骨髓增生异常综合症/急性髓细胞性白血病

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摘要

Of 1774 patients with breast cancer given mitoxantrone (MTZ) with methotrexate (n = 492) or with methotrexate and mitomycin C (n = 1282), nine developed MDS/AML after a median of 2.5 years. Median duration of survival from diagnosis of MDS/AML was 10 months and six patients died. The crude incidence of developing MDS/AML after MMM or MM chemotherapy was 15 per 100 000 patient years follow-up, while the actuarial risk was 1.1% and 1.6% at 5 and 10 years respectively. MTZ-based regimens carry a 10 × higher risk of subsequent MDS/AML compared to that seen in the general population. © 2000 Cancer Research Campaign
机译:在1774例接受甲氨蝶呤(n = 492)或甲氨蝶呤和丝裂霉素C(n = 1282)给予米托蒽醌(MTZ)的乳腺癌患者中,有9名在中位时间为2.5年后发展为MDS / AML。诊断为MDS / AML的中位生存期为10个月,有6名患者死亡。接受MMM或MM化疗后发生MDS / AML的粗略发生率为每10万患者年随访15次,而5年和10年的精算风险分别为1.1%和1.6%。与普通人群相比,基于MTZ的方案进行后续MDS / AML的风险高10倍。 ©2000癌症研究运动

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