Improved Survival for Children and Young Adults With T-Lineage Acute Lymphoblastic Leukemia: Results From the Children’s Oncology Group AALL0434 Methotrexate Randomization

医学 甲氨蝶呤 养生 内科学 中期分析 急性淋巴细胞白血病 随机化 外科 临床研究阶段 齿轮 淋巴细胞白血病 胃肠病学 白血病 化疗 临床试验 人工智能 计算机科学
作者
Stuart S. Winter,Kimberly P. Dunsmore,Meenakshi Devidas,Brent L. Wood,Natia Esiashvili,Zhiguo Chen,Nancy Eisenberg,Nikki Briegel,Robert J. Hayashi,Julie M. Gastier‐Foster,Andrew J. Carroll,Nyla A. Heerema,Barbara L. Asselin,Paul S. Gaynon,Michael J. Borowitz,Mignon L. Loh,Karen R. Rabin,Elizabeth A. Raetz,Patrick A. Zweidler‐McKay,Naomi J. Winick
出处
期刊:Journal of Clinical Oncology [American Society of Clinical Oncology]
卷期号:36 (29): 2926-2934 被引量:197
标识
DOI:10.1200/jco.2018.77.7250
摘要

Early 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.COG AALL0434 included a 2 × 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.AALL0434 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.AALL0434 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.
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