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中枢神经系统白血病的长期控制

Long-term control of central nervous system leukaemia.

作者信息

Gribbin M A, Hardisty R M, Chessells J M

出版信息

Arch Dis Child. 1977 Sep;52(9):673-8. doi: 10.1136/adc.52.9.673.

Abstract

Seventy-four children with acute lymphoblastic leukaemia had one or more episodes of central nervous system (CNS) leukaemia. 5 children had CNS involvement at diagnosis; 4 survived for less than one year. In 35 children who had not had a previous bone marrow relapse on treatment and who received combination chemotherapy, the median duration of haematological remission from the time of first CNS relapse was almost 3 years. 5 children received full dose (2400 rads) craniospinal irradiation after their first CNS relapse; 4 have remained in CNS and haematological remission for 2 1/2 years or more. 18 children who had a CNS relapse after irradiation received 4-weekly intrathecal methotrexate; in 8 children this was given via an intraventricular reservoir. The median duration of CNS remission in children receiving intrathecal methotrexate was 2 years. Systemic and intrathecal treatment was stopped in 7 children after 2 1/2 years in continuous remission and in 2 children after 2 years. 4 of these 9 children remain in remission at intervals from 41 to 69 weeks off treatment but one is severely retarded. These results show that CNS disease is compatible with prolonged survival, but illustrate the difficulties of eradicating established CNS leukaemia.

摘要

74名急性淋巴细胞白血病患儿出现了一次或多次中枢神经系统(CNS)白血病发作。5名患儿在诊断时即有中枢神经系统受累;4名存活时间不到一年。在35名治疗期间未曾有过骨髓复发且接受联合化疗的患儿中,自首次中枢神经系统复发时起血液学缓解的中位持续时间近3年。5名患儿在首次中枢神经系统复发后接受了全剂量(2400拉德)的颅脑脊髓照射;4名患儿中枢神经系统和血液学缓解已持续2年半或更长时间。18名照射后出现中枢神经系统复发的患儿接受了每4周一次的鞘内注射甲氨蝶呤;8名患儿通过脑室内储液器给药。接受鞘内注射甲氨蝶呤的患儿中枢神经系统缓解的中位持续时间为2年。7名患儿在持续缓解2年半后、2名患儿在持续缓解2年后停止了全身和鞘内治疗。这9名患儿中有4名在停止治疗41至69周期间仍处于缓解状态,但有一名严重发育迟缓。这些结果表明,中枢神经系统疾病与长期存活是相容的,但也说明了根除已确立的中枢神经系统白血病的困难。

相似文献

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Long-term control of central nervous system leukaemia.中枢神经系统白血病的长期控制
Arch Dis Child. 1977 Sep;52(9):673-8. doi: 10.1136/adc.52.9.673.
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Outcome following late marrow relapse in childhood acute lymphoblastic leukemia.
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Prevention of central nervous system leukemia by irradiation.
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Encephalopathy in acute leukaemia associated with methotrexate therapy.
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