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[慢性和急性白血病治疗的当前方面]

[Current aspects of therapy in chronic and acute leukemias].

作者信息

Seipelt G, Hoelzer D

机构信息

Medizinische Klinik III, J.-W.-Goethe-Universität, Frankfurt.

出版信息

Schweiz Med Wochenschr. 1995 Jul 11;125(27-28):1354-63.

PMID:7624746
Abstract

A significant fraction of patients with chronic myelogenous leukemia (CML) in the chronic phase have durable hematologic remissions following treatment with interferon-alpha. Some clinical trials are beginning to show a modest overall survival advantage with interferon compared to hydroxyurea. The only curative therapy for CML is allogeneic bone marrow transplantation. In chronic lymphocytic leukemia (CLL), stable early stage disease requires no treatment. Recent trials have confirmed that several new purine analogues are effective in CLL. In acute myeloid leukemias there appears to be a dose-dependent effect on remission and intensified treatment may increase the percentage of disease free survivors. Hemopoietic growth factors may reduce treatment-related morbidity and mortality. Enhancement of cytotoxicity by prestimulation with GM-CSF is still controversial. All-trans retinoic acid induces remissions in 80% of patients with acute promyelocytic leukemia by forcing the leukemic promyelocytes to maturation. Allogeneic bone marrow transplantation is effective in high risk patients with Philadelphia chromosome positive acute lymphocytic leukemia (ALL), in patients with relapse or resistant acute myelogenous leukemia (AML) or ALL. In patients with ALL a risk-adapted therapy including allogeneic and autologous bone marrow transplantation and the use of hemopoietic growth factors to improve supportive therapy may result in more cures.

摘要

慢性期慢性粒细胞白血病(CML)患者中有相当一部分在用α干扰素治疗后可获得持久的血液学缓解。一些临床试验开始显示,与羟基脲相比,干扰素在总体生存方面有适度优势。CML唯一的治愈性疗法是异基因骨髓移植。在慢性淋巴细胞白血病(CLL)中,早期病情稳定无需治疗。最近的试验证实,几种新的嘌呤类似物对CLL有效。在急性髓系白血病中,似乎对缓解存在剂量依赖性效应,强化治疗可能会增加无病生存者的比例。造血生长因子可能会降低治疗相关的发病率和死亡率。通过GM-CSF预刺激增强细胞毒性仍存在争议。全反式维甲酸通过促使白血病早幼粒细胞成熟,可使80%的急性早幼粒细胞白血病患者获得缓解。异基因骨髓移植对费城染色体阳性急性淋巴细胞白血病(ALL)的高危患者、复发或难治性急性髓系白血病(AML)或ALL患者有效。在ALL患者中,采用包括异基因和自体骨髓移植以及使用造血生长因子来改善支持治疗的风险适应性疗法可能会带来更多治愈病例。

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