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骨髓增生异常综合征患者造血多谱系反应经全反式维甲酸、粒细胞集落刺激因子、促红细胞生成素和α-生育酚联合治疗后得到改善。

Improved multilineage response of hematopoiesis in patients with myelodysplastic syndromes to a combination therapy with all-trans-retinoic acid, granulocyte colony-stimulating factor, erythropoietin and alpha-tocopherol.

作者信息

Ganser A, Maurer A, Contzen C, Seipelt G, Ottmann O G, Schadeck-Gressel C, Kolbe K, Haas R, Zander C, Reutzel R, Hoelzer D

机构信息

Department of Hematology, University of Frankfurt, Germany.

出版信息

Ann Hematol. 1996 Apr;72(4):237-44. doi: 10.1007/s002770050166.

Abstract

Differentiation induction therapy is being tested in myelodysplastic syndromes to ameliorate maturation defects and to restore normal hematopoietic function. To this end, 17 patients (eight with refractory anemia, two with refractory anemia and ring sideroblasts, and seven with refractory anemia and excess of blast cells) were treated with a combination of all-trans-retinoic acid (ATRA), granulocyte colony-stimulating factor (G-CSF), erythropoietin (EPO), and alpha-tocopherol for durations of 8-16 weeks. Absolute neutrophil counts increased in all patients; platelet counts increased in five patients with discontinuation of transfusion needs in two of four transfusion-dependent patients. Stimulation of erythropoiesis was seen in eight patients with an increase in hemoglobin concentration in three, a discontinuation of transfusion requirements in another three, and a significant increase in reticulocyte counts as the only parameter in two patients. Clinically important multilineage responses with increases of hemoglobin levels or discontinuation of transfusion needs were thus seen in six patients (35.3%) with three patients having a trilineage response. Serum erythropoietin concentrations did not differ significantly between responders and nonresponders, but the erythroid response was accompanied by a rise in the serum transferrin receptor levels. In the bone marrow, the myeloid-to-erythroid ratio and the maturation index of myeloid cells increased during therapy, while the percentage of blast cells did not change. Cytogenetic analysis demonstrated the persistence of the abnormal clones. Prior to therapy, nonresponders had a significantly higher serum TNF level than responders. Serum concentrations of TNF-alpha and soluble TNF-alpha receptor significantly increased during therapy, but mainly in the patients without an erythroid and platelet response. Soluble IL-2 receptor and soluble ICAM-1 concentrations both increased. This pilot study demonstrates that treatment with ATRA/G-CSF/EPO/tocopherol is well tolerated, leading to normalization of neutrophil counts in most, and to improvement of platelets and red blood cells in a significant subgroup of patients.

摘要

分化诱导疗法正在骨髓增生异常综合征中进行测试,以改善成熟缺陷并恢复正常造血功能。为此,17例患者(8例难治性贫血、2例难治性贫血伴环形铁粒幼细胞、7例难治性贫血伴原始细胞增多)接受了全反式维甲酸(ATRA)、粒细胞集落刺激因子(G-CSF)、促红细胞生成素(EPO)和α-生育酚联合治疗,疗程为8至16周。所有患者的绝对中性粒细胞计数均增加;5例患者血小板计数增加,4例依赖输血的患者中有2例不再需要输血。8例患者出现促红细胞生成,3例血红蛋白浓度升高,另外3例不再需要输血,2例患者网织红细胞计数显著增加为唯一参数。因此,6例患者(35.3%)出现了具有临床意义的多系反应,血红蛋白水平升高或不再需要输血,3例患者出现三系反应。反应者和无反应者的血清促红细胞生成素浓度无显著差异,但红系反应伴随着血清转铁蛋白受体水平的升高。在骨髓中,治疗期间髓系与红系比例及髓系细胞成熟指数增加,而原始细胞百分比未改变。细胞遗传学分析显示异常克隆持续存在。治疗前,无反应者的血清TNF水平显著高于反应者。治疗期间血清TNF-α和可溶性TNF-α受体浓度显著升高,但主要见于无红系和血小板反应的患者。可溶性IL-2受体和可溶性ICAM-1浓度均升高。这项初步研究表明,ATRA/G-CSF/EPO/生育酚治疗耐受性良好,多数患者中性粒细胞计数恢复正常,相当一部分患者血小板和红细胞得到改善。

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