Veerman A J, Hählen K, Kamps W A, Van Leeuwen E F, De Vaan G A, Solbu G, Suciu S, Van Wering E R, Van der Does-Van der Berg A
Dutch Childhood Leukemia Study Group, Hague, The Netherlands.
J Clin Oncol. 1996 Mar;14(3):911-8. doi: 10.1200/JCO.1996.14.3.911.
Here we report the results of a nationwide cooperative study in the Netherlands on acute lymphoblastic leukemia (ALL) in children. The aim of the study was to improve the cure rate and to minimize side effects in a group of non-high-risk ALL patients, especially with regard to the CNS. A second aim was to study potential prognostic factors.
Children (age 0 to 15 years) with non-high-risk ALL (WBC count < 50 x 10(9)/L, no mediastinal mass, no B-cell phenotype, and no CNS involvement) were treated with a uniform protocol, ALL VI. The treatment protocol used 6-week induction regimen with three drugs (vincristine, dexamethasone, and asparaginase), three weekly doses of intravenous (IV) medium high-dose methotrexate (2 g/m2), and 2-year maintenance therapy that consisted of alternating 5-week periods of methotrexate and mercaptopurine and 2-week periods of vincristine and dexamethasone. In the first year of maintenance, triple intrathecal therapy was administered every 7 weeks.
From December 1, 1984 until July 1, 1988, 291 children with ALL were diagnosed; 206 were categorized as non-high-risk (71%), and 190 were treated according to protocol ALL VI. At 8 years, the event-free survival (EFS) rate was 81% (SE = 3%) and survival rate 85% (SE = 2.9%); the median follow-up time was 7.3 years (range, 36 to 117 months). The CNS relapse rate was 1.1% (two of 184 patients who achieved a complete remission [CR]). The only factor found to be of negative prognostic importance in terms of EFS (P = .05) was a positive acid phosphatase reaction.
For children with non-high-risk ALL, the combination of IV medium high-dose methotrexate (2 g/m2 times three), triple intrathecal therapy in the first year of maintenance treatment, and the use of dexamethasone for induction and pulses during maintenance treatment has proved to be highly effective, especially in the prevention of CNS relapse. A high cure rate was achieved without the use of anthracyclines, alkylating agents, and cranial irradiation.
本文报告了荷兰一项关于儿童急性淋巴细胞白血病(ALL)的全国性合作研究结果。该研究的目的是提高一组非高危ALL患者的治愈率,并将副作用降至最低,尤其是在中枢神经系统(CNS)方面。第二个目的是研究潜在的预后因素。
对年龄在0至15岁的非高危ALL患儿(白细胞计数<50×10⁹/L,无纵隔肿块,无B细胞表型,无CNS受累)采用统一方案ALL VI进行治疗。治疗方案采用为期6周的诱导方案,使用三种药物(长春新碱、地塞米松和天冬酰胺酶),每周静脉注射(IV)中高剂量甲氨蝶呤(2 g/m²)三次,以及为期2年的维持治疗,包括甲氨蝶呤和巯嘌呤交替进行的5周疗程以及长春新碱和地塞米松的2周疗程。在维持治疗的第一年,每7周进行一次三联鞘内注射治疗。
从1984年12月1日至1988年7月1日,共诊断出291例ALL患儿;其中206例被归类为非高危(71%),190例按照ALL VI方案进行治疗。8年时,无事件生存率(EFS)为81%(标准误=3%),生存率为85%(标准误=2.9%);中位随访时间为7.3年(范围为36至117个月)。CNS复发率为1.1%(184例达到完全缓解[CR]的患者中有2例)。就EFS而言,唯一被发现具有负面预后意义的因素(P = 0.05)是酸性磷酸酶反应呈阳性。
对于非高危ALL患儿,静脉注射中高剂量甲氨蝶呤(2 g/m²×3次)、维持治疗第一年的三联鞘内注射治疗以及在诱导和维持治疗期间使用地塞米松进行脉冲治疗的联合方案已被证明非常有效,尤其是在预防CNS复发方面。在不使用蒽环类药物、烷化剂和颅脑照射的情况下实现了高治愈率。