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造血干细胞移植后用去纤苷成功治疗窦性阻塞综合征。

Successful treatment with defibrotide for sinusoidal obstruction syndrome after hematopoietic stem cell transplantation.

作者信息

Yakushijin Kimikazu, Matsui Toshimitsu, Okamura Atsuo, Yamamoto Katsuya, Ito Mitsuhiro, Chihara Kazuo

机构信息

Division of Endocrinology/Metabolism, Neurology and Hematology/Oncology, Department of Clinical Molecular Medicine, Kobe University Graduate School of Medicine.

出版信息

Kobe J Med Sci. 2005;51(3-4):55-65.

Abstract

Sinusoidal obstruction syndrome (SOS) (formerly known as hepatic veno-occlusive disease (VOD)) is a life-threatening complication subsequent to hematopoietic stem cell transplantation. However, no completely satisfactory strategies for the treatment of SOS have been established yet. Defibrotide is a single-stranded polydeoxyribonucleotide with anti-thrombotic, anti-ischemic, anti-inflammatory and thrombolytic properties, but without systemic anticoagulant effects, and some encouraging results have been reported in western countries. We treated four patients with defibrotide for SOS, since there seemed to be no possibility to cure the patients with conventionally available treatments in Japan. All patients showed evidence of multiple organ failure at the start of the treatment. Defibrotide was administered intravenously in normal saline in four divided doses for 14 to 27 days. Three patients (75%) responded to the therapy, while one died of SOS and cytomegalovirus infection despite intensive therapy. None of the patients suffered from significant adverse effects such as severe hemorrhage. This is the first report dealing with the treatment with defibrotide of Japanese patients with SOS. Because defibrotide is considered to be promising for the treatment of SOS, it is important to start a phase II study as soon as possible.

摘要

窦性阻塞综合征(SOS)(以前称为肝静脉闭塞病(VOD))是造血干细胞移植后的一种危及生命的并发症。然而,目前尚未建立完全令人满意的SOS治疗策略。去纤苷是一种具有抗血栓形成、抗缺血、抗炎和溶栓特性的单链多聚脱氧核糖核苷酸,但无全身抗凝作用,西方国家已报道了一些令人鼓舞的结果。由于在日本用常规可用的治疗方法似乎无法治愈患者,我们用去纤苷治疗了4例SOS患者。所有患者在治疗开始时均表现出多器官功能衰竭的证据。去纤苷以生理盐水静脉滴注,分4次给药,持续14至27天。3例患者(75%)对治疗有反应,而1例尽管接受了强化治疗仍死于SOS和巨细胞病毒感染。没有患者出现严重出血等明显不良反应。这是关于日本SOS患者去纤苷治疗的首次报告。由于去纤苷被认为对SOS治疗有前景,尽快开展II期研究很重要。

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