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骨髓增生异常综合征的治疗进展

Progress in the therapy of myelodysplastic syndromes.

作者信息

Boogaerts M A

机构信息

Department of Hematology, University Hospital Leuven, Belgium.

出版信息

Blut. 1989 Jun;58(6):265-70. doi: 10.1007/BF00320163.

DOI:10.1007/BF00320163
PMID:2472183
Abstract

The progress in the therapy of the myelodysplastic syndromes has been far from spectacular during recent years. No currently available treatment has been shown to be consistently effective in producing sustained improvement in hematopoiesis or in delaying leukemic evolution. With regard to both quantity and quality of life, no other treatment has been proven superior to classical supportive treatment, with the possible exception of bone marrow transplantation in younger patients. While in selected cases anecdotal successes have been noted with the use of hormonal therapy, some differentiation inducers, e.g. vitamin A- en D-analogues, have not hold their promises in placebo controlled trials. Attempts to induce complete remissions in MDS with antileukemic treatment have usually been unsuccessful. Toxicity is substantial and a considerable proportion of patients fare worse with chemotherapy than with standard supportive care. Recently, a flood of reports has appeared on the use of biological response modifiers e.g. cytokines and growth factors in the treatment of MDS. Perhaps some of these hold promises for a new era in MDS, but the data are preliminary and no follow-up on long term survival is at hand.

摘要

近年来,骨髓增生异常综合征的治疗进展并不显著。目前尚无任何一种治疗方法被证明能持续有效地改善造血功能或延缓白血病进展。在生活质量的数量和质量方面,除了年轻患者的骨髓移植可能是个例外,没有其他治疗方法被证明优于传统的支持性治疗。虽然在某些病例中使用激素治疗取得了一些成功的案例,但一些分化诱导剂,如维生素A和D类似物,在安慰剂对照试验中并未达到预期效果。试图通过抗白血病治疗诱导骨髓增生异常综合征完全缓解通常是不成功的。毒性很大,相当一部分患者接受化疗后的情况比接受标准支持性治疗更差。最近,大量关于使用生物反应调节剂(如细胞因子和生长因子)治疗骨髓增生异常综合征的报道涌现。也许其中一些对骨髓增生异常综合征的新时代有希望,但数据是初步的,目前尚无长期生存的随访结果。

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Ability of recombinant interferon gamma in vitro to restore the defective polymorphonuclear-cell- but not lymphocyte-mediated cytotoxic activities in patients with myelodysplastic syndromes.重组干扰素γ在体外恢复骨髓增生异常综合征患者缺陷性多形核细胞介导而非淋巴细胞介导的细胞毒活性的能力。
Cancer Immunol Immunother. 1992;34(6):414-8. doi: 10.1007/BF01741753.

本文引用的文献

1
Glucocorticoid therapy in the preleukemic syndrome (hemopoietic dysplasia): identification of responsive patients using in-vitro techniques.白血病前期综合征(造血发育异常)中的糖皮质激素治疗:运用体外技术识别反应性患者。
Ann Intern Med. 1980 Jan;92(1):55-8. doi: 10.7326/0003-4819-92-1-55.
2
Proposals for the classification of the myelodysplastic syndromes.骨髓增生异常综合征的分类建议。
Br J Haematol. 1982 Jun;51(2):189-99.
3
Effect of chemotherapy for the dysmyelopoietic syndrome.化疗对骨髓生成异常综合征的影响。
Cancer Treat Rep. 1981 Jul-Aug;65(7-8):601-5.
4
Chronic myelodysplastic syndrome: short survival with or without evolution to acute leukaemia.慢性骨髓增生异常综合征:无论是否演变为急性白血病,生存期均较短。
Br J Haematol. 1983 Dec;55(4):691-700. doi: 10.1111/j.1365-2141.1983.tb02852.x.
5
Phase I clinical trial of 13-cis-retinoic acid in myelodysplastic syndromes.
Cancer Treat Rep. 1983 Nov;67(11):981-6.
6
Allogeneic marrow transplantation in the treatment of preleukemia.异基因骨髓移植治疗白血病前期
Ann Intern Med. 1984 May;100(5):689-93. doi: 10.7326/0003-4819-100-5-689.
7
Blood neutrophil function in primary myelodysplastic syndromes.
Br J Haematol. 1983 Oct;55(2):217-27. doi: 10.1111/j.1365-2141.1983.tb01241.x.
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Induction of differentiation of human acute myelogenous leukemia cells: therapeutic implications.人急性髓性白血病细胞分化的诱导:治疗意义
Blood. 1983 Oct;62(4):709-21.
9
Treatment of advanced myelodysplastic syndrome with alfacalcidol.阿法骨化醇治疗晚期骨髓增生异常综合征
Lancet. 1984 Sep 29;2(8405):761. doi: 10.1016/s0140-6736(84)92676-x.
10
Myelodysplastic syndromes: a scoring system with prognostic significance.骨髓增生异常综合征:一种具有预后意义的评分系统。
Br J Haematol. 1985 Mar;59(3):425-33. doi: 10.1111/j.1365-2141.1985.tb07329.x.