Suppr超能文献

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

Interferon alpha-2b as treatment for Philadelphia-negative chronic myeloproliferative disorders with excessive thrombocytosis.

作者信息

Lazzarino M, Vitale A, Morra E, Gagliardi A, Bernasconi P, Torromeo C, Inverardi D, Burgio V, Castello A, Bernasconi C

机构信息

Division of Hematology, Istituto Scientifico Policlinico S. Matteo, Pavia, Italy.

出版信息

Br J Haematol. 1989 Jun;72(2):173-7. doi: 10.1111/j.1365-2141.1989.tb07679.x.

Abstract

We treated 32 patients with Ph1-negative chronic myeloproliferative disorders (CMD) with excessive thrombocytosis with Interferon alpha-2b (IFN alpha-2b): 26 had essential thrombocythaemia, ET (18 previously untreated, eight pretreated); one thrombocythaemia after treatment for Hodgkin's disease (HD); two thrombocythaemia associated with non-Hodgkin's lymphoma (NHL); three stage II idiopathic myelofibrosis (IM). IFN was given at daily doses of 1-4 x 10(6) IU. Twenty-seven patients (84%) responded, 17 (53%) achieved complete haematologic response after a median time of 12 weeks, and 10 (31%) partial haematologic response. Median platelet levels declined in complete haematologic response patients from 1,190 to 335 x 10(9)/l. Normalization of megakaryocyte (MK) levels was observed in 8/17 complete haematologic response patients treated for 9-12 months, with decreased bone marrow (BM) cellularity. Side effects requiring dose reduction or discontinuation of treatment occurred in 28% of cases with IFN doses of 2 or 4 x 10(6) IU. After 1 year of continuous IFN treatment, responses were maintained with conventional chemotherapy or low-dose IFN. This study demonstrates that IFN has definite therapeutic activity in CMD with excessive thrombocytosis. This biological agent, either alone or in combination with other antineoplastic treatment, may represent a new therapeutic approach for these disorders.

摘要

我们用α-2b干扰素(IFNα-2b)治疗了32例伴有血小板增多的Ph1阴性慢性骨髓增殖性疾病(CMD)患者:26例为原发性血小板增多症(ET)(18例既往未治疗,8例曾接受过治疗);1例为霍奇金病(HD)治疗后出现的血小板增多症;2例为与非霍奇金淋巴瘤(NHL)相关的血小板增多症;3例为Ⅱ期特发性骨髓纤维化(IM)。IFN的给药剂量为每日1 - 4×10⁶IU。27例患者(84%)有反应,17例(53%)在中位时间12周后达到完全血液学缓解,10例(31%)为部分血液学缓解。完全血液学缓解患者的血小板中位水平从1190降至335×10⁹/L。在17例接受9 - 12个月治疗的完全血液学缓解患者中,观察到巨核细胞(MK)水平恢复正常,同时骨髓(BM)细胞数量减少。在使用2或4×10⁶IU IFN剂量的病例中,28%出现了需要减少剂量或停止治疗的副作用。持续IFN治疗1年后,通过传统化疗或低剂量IFN维持了疗效。本研究表明,IFN在伴有血小板增多的CMD中具有明确的治疗活性。这种生物制剂单独使用或与其他抗肿瘤治疗联合使用,可能代表了这些疾病的一种新的治疗方法。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验