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地塞米松与泼尼松龙治疗儿童急性淋巴细胞白血病的疗效比较:英国医学研究委员会ALL97随机试验结果

Benefit of dexamethasone compared with prednisolone for childhood acute lymphoblastic leukaemia: results of the UK Medical Research Council ALL97 randomized trial.

作者信息

Mitchell C D, Richards S M, Kinsey S E, Lilleyman J, Vora A, Eden T O B

机构信息

Paediatric Haematology/Oncology, John Radcliffe Hospital, Oxford, UK.

出版信息

Br J Haematol. 2005 Jun;129(6):734-45. doi: 10.1111/j.1365-2141.2005.05509.x.

Abstract

Corticosteroids are an essential component of treatment for acute lymphoblastic leukaemia (ALL). Prednisolone is the most commonly used steroid, particularly in the maintenance phase of therapy. There is increasing evidence that, even in equipotent dosage for glucocorticoid effect, dexamethasone has enhanced lymphoblast cytotoxicity and penetration of the central nervous system (CNS) compared with prednisolone. Substitution of dexamethasone for prednisolone in the treatment of ALL might, therefore, result in improved event-free and overall survival. Children with newly diagnosed ALL were randomly assigned to receive either dexamethasone or prednisolone in the induction, consolidation (all received dexamethasone in intensification) and continuation phases of treatment. Among 1603 eligible randomized patients, those receiving dexamethasone had half the risk of isolated CNS relapse (P = 0.0007). Event-free survival was significantly improved with dexamethasone (84.2% vs. 75.6% at 5 years; P = 0.01), with no evidence of differing effects in any subgroup of patients. The use of 6.5 mg/m(2) dexamethasone throughout treatment for ALL led to a significant decrease in the risk of relapse for all risk-groups of patients and, despite the increased toxicity, should now be regarded as part of standard therapy for childhood ALL.

摘要

皮质类固醇是急性淋巴细胞白血病(ALL)治疗的重要组成部分。泼尼松龙是最常用的类固醇,尤其在治疗的维持阶段。越来越多的证据表明,即使在糖皮质激素作用等效剂量下,与泼尼松龙相比,地塞米松具有更强的淋巴细胞毒性和中枢神经系统(CNS)穿透力。因此,在ALL治疗中用地塞米松替代泼尼松龙可能会改善无事件生存期和总生存期。新诊断的ALL患儿在治疗的诱导、巩固(强化期均接受地塞米松)和延续阶段被随机分配接受地塞米松或泼尼松龙治疗。在1603例符合条件的随机分组患者中,接受地塞米松治疗的患者孤立性CNS复发风险减半(P = 0.0007)。地塞米松显著改善了无事件生存期(5年时为84.2%对75.6%;P = 0.01),且在任何亚组患者中均无不同效应的证据。在ALL的整个治疗过程中使用6.5mg/m²地塞米松可显著降低所有风险组患者的复发风险,尽管毒性增加,但现在应被视为儿童ALL标准治疗的一部分。

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