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α干扰素在原发性血小板增多症治疗中的应用

alpha Interferon in the management of essential thrombocythaemia.

作者信息

Giralt M, Rubio D, Cortés M T, San Miguel J, Steegmann J L, Serena J, Fernández-Rañada J M, López-Borrasca A

机构信息

Department of Hematology, Hospital Miguel Servet, Zaragoza, Spain.

出版信息

Eur J Cancer. 1991;27 Suppl 4:S72-4. doi: 10.1016/0277-5379(91)90579-3.

DOI:10.1016/0277-5379(91)90579-3
PMID:1799486
Abstract

Thirteen patients (mean age 60.7 years; female:male ratio 10:3) with essential thrombocythaemia were treated with 3 million units (MU)/day interferon alfa-2b subcutaneously (s.c.) for 12 weeks, with all patients requiring a dose reduction after 4 weeks. The mean pretreatment platelet count was 1,400 x 10(9)/L and megakaryocytes were increased in all cases. Splenomegaly was present in six patients and haemorrhagic phenomena were observed in two. Nine patients (69.2%) had objective responses, including two (15.4%) complete responses (platelets less than 450 x 10(9)/L) which were then maintained with 5 MU interferon twice a week. Acute toxicity consisted of flu-like symptoms in 12 patients. Chronic toxicity (mainly leucopenia) was observed in nine patients. In conclusion, initial therapy and then requiring maintenance therapy at a reduced dose. However, the frequent side effects observed make it advisable to use a low dose of interferon alfa-2b, and to treat only those patients with significant symptoms and signs of thrombocytosis.

摘要

13例原发性血小板增多症患者(平均年龄60.7岁;男女比例为10:3)接受皮下注射300万单位(MU)/天的干扰素α-2b治疗,疗程12周,所有患者在4周后均需减量。治疗前血小板计数平均为1400×10⁹/L,所有病例巨核细胞均增多。6例患者有脾肿大,2例观察到出血现象。9例患者(69.2%)有客观反应,其中2例(15.4%)完全缓解(血小板低于450×10⁹/L),随后以5MU干扰素每周两次维持治疗。急性毒性表现为12例患者出现流感样症状。9例患者观察到慢性毒性(主要为白细胞减少)。总之,初始治疗后需要减量维持治疗。然而,观察到的频繁副作用表明,宜使用低剂量的干扰素α-2b,且仅治疗那些有明显血小板增多症状和体征的患者。

相似文献

1
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
Eur J Cancer. 1991;27 Suppl 4:S72-4. doi: 10.1016/0277-5379(91)90579-3.
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
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.
4
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.
5
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.
6
A long-term clinical trial of interferon alpha-therapy in essential thrombocythemia.干扰素α治疗原发性血小板增多症的长期临床试验。
Ann Hematol. 1992 May;64(5):207-9. doi: 10.1007/BF01738297.
7
Alpha interferon raises serum beta-2-microglobulin in patients treated for thrombocythaemia.α干扰素可使接受血小板增多症治疗的患者血清β2-微球蛋白升高。
Br J Haematol. 1993 Jun;84(2):353-5. doi: 10.1111/j.1365-2141.1993.tb03082.x.
8
Treatment of essential thrombocythaemia by alpha 2a interferon.α2a干扰素治疗原发性血小板增多症
Lancet. 1988 Oct 22;2(8617):960-1. doi: 10.1016/s0140-6736(88)92625-6.
9
[alpha-Interferon in the treatment of essential thrombocythemia].
Rinsho Ketsueki. 1992 Feb;33(2):232-7.
10
Essential thrombocythemia--clinical features, therapy and follow-up of 12 cases.原发性血小板增多症——12例临床特征、治疗及随访
Leukemia. 1992;6 Suppl 3:138S-140S.

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Interferon alpha therapy in essential thrombocythemia and polycythemia vera-a systematic review and meta-analysis.干扰素 α 治疗原发性血小板增多症和真性红细胞增多症的系统评价和荟萃分析。
Leukemia. 2021 Jun;35(6):1643-1660. doi: 10.1038/s41375-020-01020-4. Epub 2020 Sep 1.
2
Essential thrombocythaemia: a single institution experience of 16 years.原发性血小板增多症:一家机构16年的经验
Indian J Hematol Blood Transfus. 2013 Sep;29(3):139-46. doi: 10.1007/s12288-012-0172-9. Epub 2012 Jun 26.