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escalating 静脉注射甲氨蝶呤可提高标准风险急性淋巴细胞白血病患儿的无事件生存:来自儿童肿瘤组的报告。

Escalating intravenous methotrexate improves event-free survival in children with standard-risk acute lymphoblastic leukemia: a report from the Children's Oncology Group.

机构信息

Division of Hematology-Oncology, Rainbow Babies & Children's Hospital, Case Western Reserve University, Cleveland, OH 44106, USA.

出版信息

Blood. 2011 Jul 14;118(2):243-51. doi: 10.1182/blood-2010-12-322909. Epub 2011 May 11.

Abstract

Children's Cancer Group-1991 selected 2 components from the Children's Cancer Group studies shown to be effective in high-risk acute lymphoblastic leukemia and examined them in children with National Cancer Institute standard-risk acute B-precursor lymphoblastic leukemia. These were (1) vincristine and escalating IV methotrexate (MTX) without leucovorin rescue during the interim maintenance (IM) phases and (2) addition of a second delayed intensification (DI) phase. Eligible patients (n = 2078) were randomly assigned to regimens containing either oral (PO) MTX, PO mercaptopurine, dexamethasone, and vincristine or IV MTX during IM phases, and regimens with either single DI or double DI. Five-year event-free survival (EFS) and overall survival for patients on the PO MTX arms were 88.7% ± 1.4% and 96% ± 0.9% versus 92.6% ± 1.2% and 96.5% ± 0.8% for those on the IV MTX arms (P = .009, P = .66). Five-year EFS and overall survival for patients who received single DI were 90.9% ± 1.3% and 97.1% ± 0.8% versus 90.5% ± 1.3% and 95.4% ± 3.8% for those who received double DI (P = .71, P = .12). No advantage was found for a second DI; however, replacement of PO MTX, PO mercaptopurine, vincristine, and dexamethasone during IM with vincristine and escalating IV MTX improved EFS.

摘要

儿童癌症组-1991 年从儿童癌症组的研究中选择了 2 种在高危急性淋巴细胞白血病中有效的成分,并在国家癌症研究所标准风险急性 B 前体淋巴细胞白血病患儿中进行了研究。这是(1)长春新碱和递增的 IV 甲氨蝶呤(MTX),在中期维持(IM)期间没有亚叶酸钙解救,(2)添加第二个延迟强化(DI)阶段。合格的患者(n=2078)被随机分配到含有口服(PO)MTX、PO 巯基嘌呤、地塞米松和长春新碱或 IM 期间 IV MTX 的方案,以及含有单一 DI 或双重 DI 的方案。PO MTX 臂患者的 5 年无事件生存率(EFS)和总生存率为 88.7%±1.4%和 96%±0.9%,而 IV MTX 臂患者为 92.6%±1.2%和 96.5%±0.8%(P=0.009,P=0.66)。接受单 DI 的患者 5 年 EFS 和总生存率分别为 90.9%±1.3%和 97.1%±0.8%,而接受双 DI 的患者分别为 90.5%±1.3%和 95.4%±3.8%(P=0.71,P=0.12)。第二个 DI 没有优势;然而,在 IM 期间用长春新碱和递增的 IV MTX 代替 PO MTX、PO 巯基嘌呤、长春新碱和地塞米松可提高 EFS。

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