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Glutathione S-transferase homozygous deletions and relapse in childhood acute lymphoblastic leukemia: a novel study design in a large Italian AIEOP cohort

机译:谷胱甘肽S-转移酶纯合缺失和儿童急性淋巴细胞白血病复发:在意大利AIEOP大型队列研究的一种新颖的研究设计。

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Aim: In the AIEOP-BFM 2000 trial, 15% of pediatric patients treated according to risk-adapted polychemotherapeutic regimens relapsed. The present study aimed to investigate the influence of GST-M1 and GST-T1 deletions on clinical outcome of children with acute lymphoblastic leukemia treated according to the AIEOP-BFM ALL 2000 study protocol. Materials & methods: A novel-design, two-phase study was applied to select a subsample of 614 children to be genotyped for the delations of GST genes. Cumulative incidence of relapse was then estimated by weighted Kaplan-Meier analysis, and the Cox model was applied to evaluate the effect of GST-M1 and GST-T1 isoenzyme deletions oh relapse. Results: No overall effect was found, but the GST-M1 deletion was associated with better clinical outcome within prednisone poor-responder patients (hazard ratio [HR]: 0.45; 95% Cl: 0.23-0.91; p ? 0,026), whereas the GST-T1 deletion was associated with worse outcome in the standard-risk groupv
机译:目的:在AIEOP-BFM 2000试验中,根据适应风险的多化学疗法方案治疗的小儿患者中有15%复发。本研究旨在研究根据AIEOP-BFM ALL 2000研究方案治疗的GST-M1和GST-T1缺失对急性淋巴细胞白血病儿童临床结局的影响。材料与方法:采用新颖设计的两阶段研究方法,从614名儿童的子样本中选择了要进行GST基因鉴定的基因分型。然后通过加权Kaplan-Meier分析估计复发的累积发生率,并使用Cox模型评估GST-M1和GST-T1同工酶缺失对复发的影响。结果:未发现总体效果,但在泼尼松反应较差的患者中,GST-M1缺失与较好的临床结局相关(危险比[HR]:0.45; 95%Cl:0.23-0.91; p = 0,026),而在标准风险组v

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