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首页> 外文期刊>Journal of Clinical Oncology >Improved Survival for Children and Young Adults With T-Lineage Acute Lymphoblastic Leukemia: Results From the Children's Oncology Group AALL0434 Methotrexate Randomization
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Improved Survival for Children and Young Adults With T-Lineage Acute Lymphoblastic Leukemia: Results From the Children's Oncology Group AALL0434 Methotrexate Randomization

机译:改善儿童生存和血栓急性淋巴细胞白血病的生存:儿童肿瘤学群AALL0434甲氨蝶呤随机化的结果

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摘要

PurposeEarly intensification with methotrexate (MTX) is a key component of acute lymphoblastic leukemia (ALL) therapy. Two different approaches to MTX intensification exist but had not been compared in T-cell ALL (T-ALL): the Children's Oncology Group (COG) escalating dose intravenous MTX without leucovorin rescue plus pegaspargase escalating dose, Capizzi-style, intravenous MTX (C-MTX) regimen and the Berlin-Frankfurt-Muenster (BFM) high-dose intravenous MTX (HDMTX) plus leucovorin rescue regimen.Patients and MethodsCOG AALL0434 included a 2 x 2 randomization that compared the COG-augmented BFM (ABFM) regimen with either C-MTX or HDMTX during the 8-week interim maintenance phase. All patients with T-ALL, except for those with low-risk features, received prophylactic (12 Gy) or therapeutic (18 Gy for CNS3) cranial irradiation during either the consolidation (C-MTX; second month of therapy) or delayed intensification (HDMTX; seventh month of therapy) phase.ResultsAALL0434 accrued 1,895 patients from 2007 to 2014. The 5-year event-free survival and overall survival rates for all eligible, evaluable patients with T-ALL were 83.8% (95% CI, 81.2% to 86.4%) and 89.5% (95% CI, 87.4% to 91.7%), respectively. The 1,031 patients with T-ALL but without CNS3 disease or testicular leukemia were randomly assigned to receive ABFM with C-MTX (n = 519) or HDMTX (n = 512). The estimated 5-year disease-free survival (P = .005) and overall survival (P = .04) rates were 91.5% (95% CI, 88.1% to 94.8%) and 93.7% (95% CI, 90.8% to 96.6%) for C-MTX and 85.3% (95% CI, 81.0%-89.5%) and 89.4% (95% CI, 85.7%-93.2%) for HDMTX. Patients assigned to C-MTX had 32 relapses, six with CNS involvement, whereas those assigned to HDMTX had 59 relapses, 23 with CNS involvement.ConclusionAALL0434 established that ABFM with C-MTX was superior to ABFM plus HDMTX for T-ALL in approximately 90% of patients who received CRT, with later timing for those receiving HDMTX.
机译:目的地强化甲氨蝶呤(MTX)是急性淋巴细胞白血病(全部)治疗的关键组成部分。存在两种不同的MTX强化方法,但尚未在T细胞(T-Closs)中进行比较:儿童肿瘤组(COG)升级剂量静脉内MTX,没有Leucovorin Rescue加上Pegaspargase升级剂量,Capizzi-Sique,静脉注射MTX(C -MTX)方案和柏林 - 法兰克福 - Muenster(BFM)高剂量静脉注射MTX(HDMTX)加上Leucovorin救援方案.Patiants和MethodScog AALL0434包括2×2随机化,将Cog-Cudmented BFM(ABFM)方案进行了两种C-MTX或HDMTX在8周临时维护阶段。所有患者均为T-all,除了具有低风险特征的人,在整合(C-MTX;治疗的C-MTX;治疗)或延迟强化期间接受预防性(12 GY)或治疗(CNS3)的治疗(18GY)颅辐射( HDMTX;七个月治疗)阶段。阶段,从2007年至2014年累积了1,895名患者。为所有符合条件的患者的无需符合条件的患者的无需生存和整体生存率为83.8%(95%CI,81.2%分别为86.4%)和89.5%(95%CI,87.4%至91.7%)。随机分配1,031名T-and,但没有CNS3疾病或睾丸白血病,以接受C-MTX(n = 519)或HDMTx(n = 512)的ABFM。估计的5年疾病存活(P = .005)和总存活率(P = .04)率为91.5%(95%CI,88.1%至94.8%)和93.7%(95%CI,90.8% 96.6%)对于C-MTX,85.3%(95%CI,81.0%-89.5%)和89.4%(95%CI,85.7%-93.2%)用于HDMTX。分配给C-MTX的患者已复发,六个具有CNS参与,而分配给HDMTX的人已复发59,CNS参与其中23.ConlusionAALL0434与C-MTX的ABFM均优于ABFM Plus HDMTX,在大约90中优于ABFM Plus HDMTX收到CRT的患者的百分比,稍后为那些接受HDMTX的时间。

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