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首页> 外文期刊>Journal of Clinical Oncology >Therapy-related myeloid leukemias are observed in patients with chronic lymphocytic leukemia after treatment with fludarabine and chlorambucil: results of an intergroup study, cancer and leukemia group B 9011.
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Therapy-related myeloid leukemias are observed in patients with chronic lymphocytic leukemia after treatment with fludarabine and chlorambucil: results of an intergroup study, cancer and leukemia group B 9011.

机译:在氟达拉滨和苯丁酸氮芥治疗后的慢性淋巴细胞性白血病患者中观察到与治疗相关的骨髓性白血病:一项小组间研究的结果,癌症和白血病B 9011组。

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PURPOSE: Patients with chronic lymphocytic leukemia (CLL) may have disease transformation to non-Hodgkin's lymphoma or prolymphocytic leukemia; however, development of therapy-related acute myeloid leukemia (t-AML) is unusual. A series of patients enrolled onto an intergroup CLL trial were examined for this complication. PATIENTS AND METHODS: A total of 544 previously untreated B-cell CLL patients were enrolled onto a randomized intergroup study comparing treatment with chlorambucil, fludarabine, or fludarabine plus chlorambucil. Case report forms from 521 patients were reviewed for t-AML. RESULTS: With a median follow-up of 4.2 years, six patients (1.2%) to date have developed therapy-related myelodysplastic syndrome (t-MDS; n = 3), t-AML (n = 2), or t-MDS evolving to t-AML (n = 1), from 27 to 53 months (median, 34 months) after study entry. This included five (3.5%) of 142 patients treated with fludarabine plus chlorambucil and one (0.5%) of 188 receiving fludarabine; no chlorambucil-treated patients developed t-MDS or t-AML (P =.007). At study entry, the median age among these six patients was 56 years (range, 44 to 72 years); three were male; the CLL Rai stage was I/II (n = 4) or III/IV (n = 2). Response to CLL therapy was complete (n = 4) or partial remission (n = 1) and stable disease (n = 1). Marrow cytogenetics, obtained in three of six cases at diagnosis of t-MDS or t-AML, were complex, with abnormalities in either or both chromosomes 5 and 7. Other abnormalities involved chromosomes X, 1, 8, 12, 17, and 19. Median survival after diagnosis of t-MDS/AML was 3.5 months (range, 0.5 to 10.1 months). CONCLUSION: Our findings raise the possibility that alkylator-purine analog combination therapy may increase the risk of therapy-related myeloid malignancies, which is of particular relevance with regard to ongoing trials using these combination therapies.
机译:目的:患有慢性淋巴细胞性白血病(CLL)的患者可能会转变为非霍奇金淋巴瘤或前淋巴细胞性白血病;但是,与治疗有关的急性髓细胞性白血病(t-AML)的发展并不常见。检查了参加组间CLL试验的一系列患者的并发症。患者和方法:总共544名先前未接受治疗的B细胞CLL患者参加了一项随机分组研究,比较了苯丁酸氮芥,氟达拉滨或氟达拉滨加苯丁酸氮芥的治疗。审查了521例患者的病例报告表中的t-AML。结果:中位随访时间为4.2年,迄今已有6例患者(1.2%)发生了与治疗相关的骨髓增生异常综合征(t-MDS; n = 3),t-AML(n = 2)或t-MDS在进入研究后27到53个月(中位数为34个月)演变为t-AML(n = 1)。其中包括接受氟达拉滨加苯丁酸氮芥治疗的142例患者中的5例(3.5%)和接受氟达拉滨的188例患者中的1例(0.5%);没有苯丁酸氮芥治疗的患者发生t-MDS或t-AML(P = .007)。在研究开始时,这六名患者的中位年龄为56岁(范围为44至72岁)。三是男性; CLL Rai阶段为I / II(n = 4)或III / IV(n = 2)。对CLL疗法的反应完全(n = 4)或部分缓解(n = 1)且疾病稳定(n = 1)。在诊断为t-MDS或t-AML的6例病例中,有3例获得了骨髓细胞遗传学,很复杂,在5号和7号染色体中或其中一个均具有异常。诊断为t-MDS / AML后的中位生存期为3.5个月(范围为0.5到10.1个月)。结论:我们的发现增加了烷化剂-嘌呤类似物联合疗法可能增加与治疗相关的骨髓恶性肿瘤风险的可能性,这与正在进行的使用这些联合疗法的试验特别相关。

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