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用干扰素α-2b治疗慢性骨髓增殖性疾病中的血小板增多症。

Treatment of thrombocytosis in chronic myeloproliferative disorders with interferon alfa-2b.

作者信息

Seewann H L, Zikulnig R, Gallhofer G, Schmid C

机构信息

III Department of Medicine, County Hospital, Graz, Austria.

出版信息

Eur J Cancer. 1991;27 Suppl 4:S58-62; discussion S62-3. doi: 10.1007/978-3-642-75510-1_71.

DOI:10.1007/978-3-642-75510-1_71
PMID:1799482
Abstract

Thirty-six patients with chronic myeloproliferative disorders (CMPD) with thrombocytosis (essential thrombocythaemia 19 patients, chronic megakaryocytic granulocytic myelosis five, polycythaemia vera six, chronic myelogenous leukaemia six) were treated with interferon alfa-2b to reduce the platelet count. The pre-treatment platelet count was in the range 450-700 x 10(9)/L in eight patients, 700-1000 x 10(9)/L in eight and above 1000 x 10(9)/L in 20. In the induction phase of treatment 22 patients were treated with interferon alfa-2b 3 million units (MU) daily subcutaneously for 2 months or until the platelet count returned to normal, if earlier. Fourteen patients received 5 MU interferon alfa-2b daily in the same way. In the maintenance phase the doses were reduced to 3 MU and 5 MU thrice weekly, respectively. Complete response (CR), defined as a reduction of platelet count to below 450 x 10(9)/L, was achieved in 78% of patients (within 2 months of induction in 64%). The platelet depleting effect was dose dependent: CR in 2 months in 52% on 3 MU interferon alfa-2b versus 75% on 5 MU. Reduction of interferon dose was followed by an increase in platelet count in 39% of patients. The white cell count fell by 50% in Philadelphia-negative CMPD. Side effects were common, though generally mild, but led to withdrawal of treatment in six patients. Three patients suffered cerebrovascular events during treatment and one shortly thereafter.

摘要

36例慢性骨髓增殖性疾病(CMPD)伴血小板增多症患者(原发性血小板增多症19例、慢性巨核细胞粒细胞性骨髓增生症5例、真性红细胞增多症6例、慢性粒细胞白血病6例)接受了α-2b干扰素治疗以降低血小板计数。8例患者治疗前血小板计数在450 - 700×10⁹/L之间,8例在700 - 1000×10⁹/L之间,20例高于1000×10⁹/L。在治疗诱导期,22例患者皮下注射α-2b干扰素300万单位(MU),每日1次,共2个月,或血小板计数恢复正常(若更早恢复正常则提前结束)。14例患者以同样方式接受5MUα-2b干扰素每日治疗。在维持期,剂量分别减至3MU和5MU,每周3次。完全缓解(CR)定义为血小板计数降至450×10⁹/L以下,78%的患者达到完全缓解(64%在诱导期2个月内达到)。血小板减少效应呈剂量依赖性:接受3MUα-2b干扰素治疗的患者中52%在2个月内达到CR,而接受5MU治疗的患者中这一比例为75%。39%的患者在减少干扰素剂量后血小板计数升高。费城染色体阴性的CMPD患者白细胞计数下降50%。副作用常见,虽一般较轻,但6例患者因此停止治疗。3例患者在治疗期间发生脑血管事件,1例在治疗后不久发生。

相似文献

1
Treatment of thrombocytosis in chronic myeloproliferative disorders with interferon alfa-2b.用干扰素α-2b治疗慢性骨髓增殖性疾病中的血小板增多症。
Eur J Cancer. 1991;27 Suppl 4:S58-62; discussion S62-3. doi: 10.1007/978-3-642-75510-1_71.
2
alpha Interferon treatment of essential thrombocythaemia and other myeloproliferative disorders with excessive thrombocytosis.α干扰素治疗原发性血小板增多症及其他伴有血小板过度增多的骨髓增殖性疾病。
Eur J Cancer. 1991;27 Suppl 4:S69-71. doi: 10.1016/0277-5379(91)90578-2.
3
[Alfa-2b interferon in the treatment of thrombocytosis associated to chronic non leukemic myeloproliferative syndromes].
Med Clin (Barc). 1993 Nov 13;101(16):601-3.
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Treatment of thrombocytosis in myeloproliferative disorders with interferon alpha-2a.用α-2a干扰素治疗骨髓增殖性疾病中的血小板增多症。
Blut. 1989 Jan;58(1):15-9. doi: 10.1007/BF00320230.
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alpha Interferon in the management of essential thrombocythaemia.α干扰素在原发性血小板增多症治疗中的应用
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Interferon alpha-2b as treatment for Philadelphia-negative chronic myeloproliferative disorders with excessive thrombocytosis.干扰素α-2b治疗伴有血小板增多症的费城染色体阴性慢性骨髓增殖性疾病
Br J Haematol. 1989 Jun;72(2):173-7. doi: 10.1111/j.1365-2141.1989.tb07679.x.
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Maintenance therapy in the myeloproliferative disorders: the current options.骨髓增殖性疾病的维持治疗:当前的选择。
Br J Haematol. 1991 Oct;79 Suppl 1:92-5. doi: 10.1111/j.1365-2141.1991.tb08130.x.
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[Interferon therapy in essential thrombocythemia].[原发性血小板增多症的干扰素治疗]
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Interferon alpha-2b in the long-term treatment of essential thrombocythemia.干扰素α-2b用于原发性血小板增多症的长期治疗。
Ann Hematol. 1991 Oct;63(4):206-9. doi: 10.1007/BF01703444.
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Recombinant interferon-alpha therapy of Philadelphia chromosome-negative myeloproliferative disorders with thrombocytosis.采用重组α干扰素治疗伴有血小板增多症的费城染色体阴性骨髓增殖性疾病。
Am J Med. 1989 May;86(5):554-8. doi: 10.1016/0002-9343(89)90384-7.

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