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首页> 外文期刊>Blood: The Journal of the American Society of Hematology >Gemtuzumab ozogamicin as postconsolidation therapy does not prevent relapse in children with AML: Results from NOPHO-AML 2004
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Gemtuzumab ozogamicin as postconsolidation therapy does not prevent relapse in children with AML: Results from NOPHO-AML 2004

机译:Gemtuzumab ozogamicin作为巩固治疗后不能预防AML儿童复发:NOPHO-AML 2004的结果

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There are no data on the role of postconsolidation therapy with gemtuzumab ozogamicin (GO; Mylotarg) in children with acute myeloid leukemia (AML). The NOPHO-AML 2004 protocol studied postconsolidation randomization to GO or no further therapy. GO was administered at 5 mg/m2 and repeated after 3 weeks. We randomized 120 patients; 59 to receive GO. Survival was analyzed on an intention-to-treat basis. The median follow-up for patients who were alive was 4.2 years. Children who received GO showed modest elevation of transaminase and bilirubin without signs of venoocclusive disease. Severe neutropenia followed 95% and febrile neutropenia 40% of the GO courses. Only a moderate decline in platelet count and a minor decrease in hemoglobin occurred. Relapse occurred in 24 and 25 of those randomized to GO or no further therapy. The median time to relapse was 16 months versus 10 months (nonsignificant). The 5-year event-free survival and overall survival was 55% versus 51% and 74% versus 80% in those randomized to receive GO or no further therapy, respectively. Results were similar in all subgroups. In conclusion, GO therapy postconsolidation as given in this trial was well tolerated, showed a nonsignificant delay in time to relapse, but did not change the rate of relapse or survival (clinicaltrials.gov identifier NCT00476541).
机译:目前尚无关于吉妥单抗ozogamicin(GO; Mylotarg)合并后治疗在急性髓性白血病(AML)儿童中的作用的数据。 NOPHO-AML 2004方案研究了巩固后随机分配至GO或无进一步治疗的可能性。 GO的剂量为5 mg / m2,3周后重复给药。我们随机分配了120名患者; 59接收GO。以意向性治疗为基础分析生存率。存活患者的中位随访时间为4.2年。接受GO治疗的儿童的转氨酶和胆红素水平适度升高,而没有静脉闭塞性疾病的迹象。重度中性粒细胞减少症占GO疗程的95%,高热性中性粒细胞减少症占40%。仅发生血小板计数的中度下降和血红蛋白的轻微下降。随机分为GO或无进一步治疗者中有24和25例复发。复发的中位时间为16个月,而10个月(无统计学意义)。随机接受GO或不接受进一步治疗的患者的5年无事件生存率和总生存率分别为55%,51%和74%和80%。所有亚组的结果均相似。综上所述,在该试验中,GO治疗巩固后的耐受性良好,复发时间无明显延迟,但未改变复发率或生存率(clinicaltrials.gov标识符NCT00476541)。

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