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Treatment of acute lymphoblastic leukemia in Hong Kong children: HKALL 93 study.

机译:香港儿童的急性淋巴细胞白血病的治疗:HKALL 93研究。

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A population-based multicentre study for childhood acute lymphoblastic leukemia (ALL) was conducted in Hong Kong from 1993 to 1997. One hundred and forty-five newly diagnosed ALL patients were treated by the HKALL 93 protocol. Patients were stratified into three risk groups according to age, presenting white cell count, immunophenotyping and cytogenetic study. The patients received the same induction and early and late intensification at week 5 and week 20. Fifty-eight standard risk (SR) patients received regular intrathecal methotrexate as CNS preventive therapy, while 49 intermediate risk (IR) patients received high dose intravenous methotrexate and regular intrathecal methotrexate. Thirty-eight high risk (HR) patients were treated with prophylactic cranial irradiation and an additional intensification block at week 35. The induction remission rate was 97.2% with 2% induction death. Two patients died during first complete remission. Relapse occurred in 20.7, 42.9 and 42.1% of SR, IR and HR patients respectively. By multivariate logistic regression, age>/=10 years and white cell count>/=100x10(9)/l were the two significant variables accounting for mortality. The 5-year overall and event-free survival of the whole group was 81.3 and 62.6% respectively. According to risk groups, the event-free survival was 79, 49 and 61% for SR, IR and HR patients respectively, while the overall survival was 96, 73 and 68% for SR, IR and HR patients respectively. In conclusion, the treatment protocol had low treatment-related mortality but was associated with a rather high relapse rate, especially in IR patients. Salvage therapy achieved sustained second remission in some patients. More intensive treatment especially a late intensification is required to improve the outcome. Copyright 2002 John Wiley & Sons, Ltd.
机译:1993年至1997年在香港进行了一项基于人群的儿童急性淋巴细胞白血病(ALL)多中心研究。HKALL93方案治疗了145例新诊断的ALL患者。根据年龄将患者分为三个风险组,分别进行白细胞计数,免疫表型和细胞遗传学研究。在第5周和第20周,患者接受相同的诱导和早期和晚期强化治疗。58名标准风险(SR)患者接受定期鞘内注射甲氨蝶呤作为中枢神经系统预防性治疗,而49名中等风险(IR)患者接受大剂量静脉注射甲氨蝶呤和治疗。定期鞘内注射甲氨蝶呤。在第35周时,对38例高危(HR)患者进行了预防性颅脑照射和额外的强化阻断治疗。诱导缓解率为97.2%,诱导死亡为2%。首次完全缓解期间有两名患者死亡。 SR,IR和HR患者分别发生复发,分别占20.7%,42.9%和42.1%。通过多元逻辑回归分析,年龄> / = 10岁和白细胞计数> / = 100x10(9)/ l是造成死亡率的两个重要变量。整个组的5年总生存率和无事件生存率分别为81.3和62.6%。根据风险人群,SR,IR和HR患者的无事件生存率分别为79%,49%和61%,而SR,IR和HR患者的总生存率分别为96%,73%和68%。总之,该治疗方案的治疗相关死亡率较低,但复发率较高,尤其是在IR患者中。打捞疗法使部分患者获得了持续的第二次缓解。需要更深入的治疗,尤其是后期强化治疗,以改善疗效。版权所有2002 John Wiley&Sons,Ltd.

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