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[儿童急性淋巴细胞白血病治疗方案的最终结果及对比分析]

[End results and comparative analysis of treatment programs for childhood acute lymphocytic leukemia].

作者信息

Kawai S, Fujimoto T

出版信息

Gan To Kagaku Ryoho. 1987 Jan;14(1):17-26.

PMID:3467655
Abstract

The outcome of sixteen treatment programs for childhood acute lymphocytic leukemia reported by cooperative study groups were reviewed and analysed. The rate of disease-free survival for 3 years or more ranged from 34% to 75%, depending on each clinical trial. Remission induction therapy always consists of at least vincristine (V) and prednisone (P). L-asparaginase or daunorubicin is generally added to VP therapy. The following central nervous system (CNS) prophylaxis therapies were compared: craniospinal irradiation cranial irradiation (either 2400 rads or 1800 rads) plus intrathecal methotrexate, intrathecal drugs (either methotrexate alone or so-called triple therapy consisting of methotrexate, cytosine arabinoside and hydrocortisone) and intermediate- or high-dose methotrexate plus intrathecal methotrexate. These therapies have reduced the incidence of CNS leukemia to less than 10%. The intensification phase was the most variable component of treatment. In order to obtain maximum leukemic cell killing early in treatment, a number of protocols are investigating the use of an intensive consolidation course. An early consolidation study by the Berlin-Munster-Frankfurt group in West Germany achieved successful results. However, intensive therapy for low-risk patients failed to improve the disease-free survival. Further studies will be needed to assess the effectiveness of prolonged intensification for patients having any of the prognostic risk features. The standard duration of therapy varies between 2 and 3 years, but the minimum duration of effective chemotherapy is still unknown. It should be clarified whether a more intensive chemotherapy, can facilitate a shorter duration of treatment.

摘要

对合作研究小组报告的16种儿童急性淋巴细胞白血病治疗方案的结果进行了回顾和分析。3年或更长时间的无病生存率在34%至75%之间,具体取决于每项临床试验。缓解诱导治疗通常至少包括长春新碱(V)和泼尼松(P)。左旋门冬酰胺酶或柔红霉素通常会添加到VP治疗中。对以下中枢神经系统(CNS)预防疗法进行了比较:全脑全脊髓照射、颅脑照射(2400拉德或1800拉德)加鞘内注射甲氨蝶呤、鞘内药物(单独使用甲氨蝶呤或由甲氨蝶呤、阿糖胞苷和氢化可的松组成的所谓三联疗法)以及中剂量或高剂量甲氨蝶呤加鞘内注射甲氨蝶呤。这些疗法已将中枢神经系统白血病的发病率降低至10%以下。强化阶段是治疗中变化最大的部分。为了在治疗早期最大程度地杀伤白血病细胞,许多方案正在研究使用强化巩固疗程。西德柏林-明斯特-法兰克福小组进行的一项早期巩固研究取得了成功结果。然而,低风险患者的强化治疗未能提高无病生存率。需要进一步研究来评估延长强化治疗对具有任何预后风险特征患者的有效性。治疗的标准持续时间在2至3年之间,但有效化疗的最短持续时间仍不清楚。应明确更强化的化疗是否可以缩短治疗持续时间。

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