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儿童急性淋巴细胞白血病两种强化治疗方案的比较结果:柏林-法兰克福-明斯特方案与达纳-法伯癌症研究所方案

Comparative results of two intensive treatment programs for childhood acute lymphoblastic leukemia: The Berlin-Frankfurt-Münster and Dana-Farber Cancer Institute protocols.

作者信息

Niemeyer C M, Reiter A, Riehm H, Donnelly M, Gelber R D, Sallan S E

机构信息

Kinderklinik der Medizinischen Hochschule, Hannover, FRG.

出版信息

Ann Oncol. 1991 Nov-Dec;2(10):745-9. doi: 10.1093/oxfordjournals.annonc.a057856.

Abstract

We analyzed two of the most successful trials for childhood acute lymphoblastic leukemia, from the Berlin-Frankfurt-Münster group (BFM) and the Dana-Farber Cancer Institute (DFCI), to determine their similarities and differences and suggest ways to improve future treatments. Protocol ALL-BFM 81 (n = 611) was conducted between 1981-1983 in 37 centers in West Germany and Austria; Protocol DFCI 81-01 (n = 286) was conducted between 1981-1985 in seven centers within the United States. The BFM study used a risk score, based on peripheral lymphoblast count, liver size, and spleen size at the time of diagnosis to assign patients into one of the three treatment arms. The DFCI study classified patients into two groups: standard risk patients (age 2-9 years, with white blood count less than 20,000/mm3, and with no T-cell markers, mediastinal mass, nor central nervous system disease), and high risk patients (all others). Both studies involved intensive chemotherapy, although treatment strategies, cumulative drug doses and cranial radiation protocols differed. Study populations in the two trials were comparable with respect to age, sex, white blood count and proportion of patients with T-cell markers at the time of diagnosis. Using DFCI risk group criteria, 37% of BFM and 38% of DFCI patients were classified as standard risk. Median follow-up times were 6.8 years and 6.1 years, respectively.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们分析了柏林-法兰克福-明斯特协作组(BFM)和丹娜-法伯癌症研究所(DFCI)开展的两项针对儿童急性淋巴细胞白血病最成功的试验,以确定它们的异同,并提出改进未来治疗方法的建议。ALL-BFM 81方案(n = 611)于1981年至1983年在西德和奥地利的37个中心进行;DFCI 81-01方案(n = 286)于1981年至1985年在美国境内的7个中心进行。BFM研究采用了一种风险评分方法,该方法基于诊断时的外周血淋巴细胞计数、肝脏大小和脾脏大小,将患者分为三个治疗组之一。DFCI研究将患者分为两组:标准风险患者(年龄2至9岁,白细胞计数低于20,000/mm³,且无T细胞标志物、纵隔肿块或中枢神经系统疾病)和高风险患者(其他所有患者)。两项研究均涉及强化化疗,不过治疗策略、累积药物剂量和颅脑放疗方案有所不同。两项试验中的研究人群在年龄、性别、白细胞计数以及诊断时具有T细胞标志物的患者比例方面具有可比性。按照DFCI风险组标准,BFM组37%的患者和DFCI组38%的患者被归类为标准风险。中位随访时间分别为6.8年和6.1年。(摘要截选于250字)

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