Chessells J M, Bailey C C, Richards S
Leukemia. 1992;6 Suppl 2:157-61.
MRC UKALL X, the successor of UKALL VIII ran from 1985 to 1990 and accrued 1614 patients aged 0-15 years. After standard induction all children except those with initial white cell count greater than 100 x 10(9)/1 were randomised to one of four regimens; +/- early intensification +/- late intensification. CNS protection for all comprised cranial irradiation and intrathecal methotrexate with continuing treatment for two years. At a median follow up of four years the overall event free survival for all children is 66% (SE 1.5). This is a significant improvement over the previous MRC UKALL VIII trial. Age, sex and leucocyte count were highly significant prognostic factors. Analysis of the results indicates that the regimen containing both intensifications is superior. The strategy of early and late intensification has been adopted in the successor protocol MRC UKALL XI in which patients are additionally randomised to receive high dose methotrexate.
英国医学研究理事会(MRC)UKALL X是UKALL VIII的后续试验,从1985年持续至1990年,纳入了1614名0至15岁的患者。在进行标准诱导治疗后,除初始白细胞计数大于100×10⁹/L的儿童外,所有儿童被随机分配至四种治疗方案之一;±早期强化治疗±晚期强化治疗。所有患者的中枢神经系统保护措施包括颅脑照射和鞘内注射甲氨蝶呤,并持续治疗两年。在中位随访四年时,所有儿童的总体无事件生存率为66%(标准误1.5)。这相较于之前的MRC UKALL VIII试验有显著改善。年龄、性别和白细胞计数是高度显著的预后因素。结果分析表明,包含两种强化治疗的方案更优。早期和晚期强化治疗策略已被后续的MRC UKALL XI方案采用,该方案中患者还被随机分配接受大剂量甲氨蝶呤治疗。