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α干扰素治疗成人系统性肥大细胞增多症:一项针对20例患者的多中心II期试验结果

Treatment of adult systemic mastocytosis with interferon-alpha: results of a multicentre phase II trial on 20 patients.

作者信息

Casassus Philippe, Caillat-Vigneron Nadine, Martin Antoine, Simon Jeanne, Gallais Valérie, Beaudry Patrice, Eclache Virginie, Laroche Liliane, Lortholary Pierre, Raphaël Martine, Guillevin Loïc, Lortholary Olivier

机构信息

Service d'Hématologie Clinique, Hôpital Avicenne, Université Paris-Nord, Bobigny, Paris, France.

出版信息

Br J Haematol. 2002 Dec;119(4):1090-7. doi: 10.1046/j.1365-2141.2002.03944.x.

Abstract

Systemic mastocytosis (SM) is characterized by proliferation of mast cells in various organs, which may release a wide variety of mediators, thereby explaining the broad clinical spectrum of disease manifestations. The potentially life-threatening systemic symptoms and tumoral proliferation are poorly controlled despite the use of several cytotoxic chemotherapies and/or symptomatic treatments. Twenty consecutive adult SM patients with histologically confirmed bone marrow (BM) involvement received interferon-alpha subcutaneously (1-5 million units/m2/d, with progressive dose intensification over the first month of treatment) and were evaluated after 6 months of therapy. Seven of them had previously received symptomatic treatments, including steroids, which were ineffective. Among the 13 patients treated for at least 6 months, seven partial and six minor responses, mainly concerning vascular congestion and skin lesions, were obtained, while BM infiltration remained unchanged in 12 patients. The significant reduction of mast-cell mediator levels after 6 months of treatment was not predictive of clinical remission. The rate of depression was unexpectedly high (seven patients; 35%). Two patients died soon after starting therapy (one myocardial infarction, one septic shock). Six months of interferon-alpha may relieve vascular congestion in adults with SM, probably by inhibiting mast-cell degranulation.

摘要

系统性肥大细胞增多症(SM)的特征是肥大细胞在各个器官中增殖,这些肥大细胞可能释放多种介质,从而解释了该病临床表现的广泛范围。尽管使用了多种细胞毒性化疗药物和/或对症治疗,但潜在的危及生命的全身症状和肿瘤增殖仍难以得到有效控制。连续20例经组织学证实有骨髓(BM)受累的成年SM患者接受皮下注射α干扰素(100万 - 500万单位/m²/天,在治疗的第一个月逐渐增加剂量强度),并在治疗6个月后进行评估。其中7例患者此前接受过包括类固醇在内的对症治疗,但均无效。在接受至少6个月治疗的13例患者中,获得了7例部分缓解和6例轻微缓解,主要涉及血管充血和皮肤病变,而12例患者的骨髓浸润情况未变。治疗6个月后肥大细胞介质水平的显著降低并不能预测临床缓解。抑郁发生率出乎意料地高(7例患者,占35%)。两名患者在开始治疗后不久死亡(1例心肌梗死,1例感染性休克)。α干扰素治疗6个月可能通过抑制肥大细胞脱颗粒缓解成年SM患者的血管充血。

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