Chessells Judith M, Harrison Georgina, Richards Susan M, Gibson Brenda E, Bailey Clifford C, Hill Frank G H, Hann Ian M
Molecular Haematology Unit, Camelia Botnar Laboratories, Institute of Child Health, 30 Guilford Street, London WC1N 1EH, UK.
Br J Haematol. 2002 Aug;118(2):445-55. doi: 10.1046/j.1365-2141.2002.03647.x.
The impact of various types of intensification therapy was examined in a cohort of 3617 children aged 1-14 years with acute lymphoblastic leukaemia (ALL) enrolled in the Medical Research Council (MRC) UKALL X (1985-90) and UKALL XI (1990-97) trials. UKALL XI was modified in 1992 to incorporate the "best arm" of UKALL X with two 5-d intensification blocks at 5 and 20 weeks, and an additional randomization in respect of a third intensification at 35 weeks but omission of two consecutive injections of daunorubicin during induction. All children were eligible for randomization irrespective of risk group. The impact of the various types of intensification therapy was examined in a stratified analysis. At a median follow up of 102 months, both trials had an identical event-free survival of 61% (95% CI 58-63%) at 8 years. Survival at 8 years in UKALL XI was significantly better in than in UKALL X, 81% (79-83%) compared with 74% (72-76%) (P = < 0.001), owing to improved management of relapse. There was a highly significant trend in reduction of the number of relapses and deaths with increased intensity of therapy both for children with initial leucocyte count < 50 x 10(9)/l (P = < 0.001) and > or = 50 x 10(9)/l (P = 0.002). Introduction of a third late intensification block compensated for omission of anthracyclines during induction but produced little additional benefit. These results show, in a large cohort of patients, that minor modifications of therapy may influence relapse rate and obviate the benefit of previous randomized trials. The failure to adapt treatment for higher risk children contributed to these disappointing results.
在一项针对3617名1至14岁急性淋巴细胞白血病(ALL)儿童的队列研究中,考察了不同类型强化治疗的效果。这些儿童参加了英国医学研究理事会(MRC)的UKALL X(1985 - 1990年)和UKALL XI(1990 - 1997年)试验。UKALL XI在1992年进行了修改,纳入了UKALL X的“最佳方案”,即在第5周和第20周有两个为期5天的强化疗程,并且在第35周进行了关于第三次强化的额外随机分组,但在诱导期省略了连续两次柔红霉素注射。所有儿童无论风险分组如何均有资格参与随机分组。通过分层分析考察了不同类型强化治疗的效果。在中位随访102个月时,两项试验在8年时的无事件生存率均为61%(95%置信区间58 - 63%)。由于对复发的管理得到改善,UKALL XI在8年时的生存率显著高于UKALL X,分别为81%(79 - 83%)和74%(72 - 76%)(P = < 0.001)。对于初始白细胞计数<50×10⁹/L(P = < 0.001)和≥50×10⁹/L(P = 0.002)的儿童,随着治疗强度增加,复发和死亡数量减少的趋势非常显著。引入第三个晚期强化疗程弥补了诱导期蒽环类药物的省略,但几乎没有带来额外益处。这些结果表明,在一大群患者中,治疗的微小改变可能会影响复发率,使先前随机试验的益处失效。未能针对高风险儿童调整治疗导致了这些令人失望的结果。