首页> 外文期刊>European journal of cancer: official journal for European Organization for Research and Treatment of Cancer (EORTC) [and] European Association for Cancer Research (EACR) >The low incidence of secondary acute myelogenous leukaemia in children and adolescents treated with dexrazoxane for acute lymphoblastic leukaemia: a report from the Dana-Farber Cancer Institute ALL Consortium.
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The low incidence of secondary acute myelogenous leukaemia in children and adolescents treated with dexrazoxane for acute lymphoblastic leukaemia: a report from the Dana-Farber Cancer Institute ALL Consortium.

机译:右雷佐生治疗急性淋巴细胞白血病的儿童和青少年继发性急性骨髓性白血病的发生率低:Dana-Farber癌症研究所ALL联合会的报告。

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摘要

BACKGROUND: Dexrazoxane reduces the risk of anthracycline-related cardiotoxicity. In a study of children with Hodgkin lymphoma, the addition of dexrazoxane may have been associated with a higher risk for developing second malignant neoplasms (SMNs) including acute myelogenous leukaemia (AML) and myelodysplastic syndrome (MDS). We determined the incidence of SMNs in children and adolescents with acute lymphoblastic leukaemia (ALL) who were treated with dexrazoxane. METHODS: Between 1996 and 2010, the Dana-Faber Cancer Institute ALL Consortium conducted three consecutive multicentre trials for children with newly diagnosed ALL. In the first (1996-2000), high risk patients were randomly assigned to receive doxorubicin (30mg/m(2)/dose, cumulative dose 300mg/m(2)) preceded by dexrazoxane (300mg/m(2)/dose, 10 doses), or the same dose of doxorubicin without dexrazoxane, during induction and intensification phases. In subsequent trials (2000-2005 and 2005-2010), all high risk and very high risk patients received doxorubicin preceded by dexrazoxane. Cases of SMNs were collected prospectively and were pooled for analysis. The frequency and 5-year cumulative incidence (CI) of SMNs were determined for patients who had received dexrazoxane. FINDINGS: Among 553 patients treated with dexrazoxane (1996-2000, N=101; 2000-2005, N=196; and 2005-2010, N=256), the number of SMNs observed by protocol was 0 (median follow-up 9.6years), 0 (median follow-up 5.2years), and 1 (median follow-up 2.1years). The only SMN was a case of AML, which developed in a patient with MLL-rearranged ALL 2.14years after initial diagnosis. The overall 5-year CI of SMNs for all 553 patients was 0.24+/-0.24%. INTERPRETATION: In a large population of children with high risk ALL who received dexrazoxane as a cardioprotectant drug, the occurrence of secondary AML was a rare event.
机译:背景:右雷佐生降低了蒽环类药物相关心脏毒性的风险。在一项针对霍奇金淋巴瘤儿童的研究中,添加右雷佐生可能与罹患包括急性骨髓性白血病(AML)和骨髓增生异常综合症(MDS)在内的第二恶性肿瘤(SMN)的风险较高相关。我们确定了接受右雷佐生治疗的急性淋巴细胞白血病(ALL)儿童和青少年中SMN的发生率。方法:1996年至2010年,达纳-法伯癌症研究所ALL协会对新诊断为ALL的儿童进行了三个连续的多中心试验。在第一个(1996-2000年)中,高危患者被随机分配接受阿霉素(30mg / m(2)/剂量,累积剂量300mg / m(2)),然后是右雷佐生(300mg / m(2)/剂量, 10剂),或在诱导和强化阶段使用相同剂量的阿霉素而不使用右雷佐生。在随后的试验(2000-2005年和2005-2010年)中,所有高危和极高危患者均先接受阿霉素,然后接受右雷佐生。前瞻性收集SMN的病例,并汇总以进行分析。确定了接受右雷佐生治疗的患者SMN的发生频率和5年累积发生率(CI)。结果:在接受右雷佐生治疗的553例患者中(1996-2000年,N = 101; 2000-2005年,N = 196; 2005-2010年,N = 256),方案观察到的SMN数量为0(中位随访9.6)年),0(中位随访时间为5.2年)和1(中位随访时间为2.1年)。唯一的SMN是AML,这是在初诊后2.14年经MLL重排的ALL患者发展而成的。所有553例患者的SMN总体5年CI为0.24 +/- 0.24%。解释:在接受右雷佐生作为心脏保护药的高危ALL儿童中,继发性AML的发生是罕见的。

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