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肥大细胞增多症患者的当前治疗选择:2015年现状与未来展望

Current treatment options in patients with mastocytosis: status in 2015 and future perspectives.

作者信息

Arock Michel, Akin Cem, Hermine Olivier, Valent Peter

机构信息

Molecular Oncology and Pharmacology, LBPA CNRS UMR8113, Ecole Normale Supérieure de Cachan, Cachan, France.

Laboratory of Hematology, Pitié-Salpêtrière Hospital, Paris, France.

出版信息

Eur J Haematol. 2015 Jun;94(6):474-90. doi: 10.1111/ejh.12544. Epub 2015 Mar 26.

Abstract

Mastocytosis is a term referring to a heterogeneous group of disorders characterized by abnormal mast cell (MC) accumulation in the skin and/or internal organs. In children, the disease involves mostly the skin (cutaneous mastocytosis; CM), whereas in adults, the disease is usually systemic (systemic mastocytosis; SM). Advanced SM variants with end-organ damage and reduced life expectancy have also been described, but are rare. Clinical signs and symptoms in SM result from excessive mediator release by MCs and, in aggressive forms, from organ failure related to MC infiltration. As a consequence, treatment of indolent SM aims primarily at the control of symptoms caused by MC mediator release. By contrast, in advanced SM, such as aggressive SM, MC leukemia, and MC sarcoma, intensive (chemo)therapy with or without allogeneic stem cell transplantation has to be considered. In addition, activating mutations in KIT (mostly KIT D816V in adults) are found in most patients with SM, so that targeted therapies aimed at blocking mutant KIT variants or/and downstream signaling pathways are currently being developed. Other targets, such as specific surface antigens expressed on neoplastic MCs, might be considered for the development of future therapies in advanced SM.

摘要

肥大细胞增多症是一个术语,指的是一组异质性疾病,其特征是肥大细胞(MC)在皮肤和/或内脏器官中异常积聚。在儿童中,该疾病主要累及皮肤(皮肤肥大细胞增多症;CM),而在成人中,该疾病通常是全身性的(系统性肥大细胞增多症;SM)。也有关于伴有终末器官损害和预期寿命缩短的晚期SM变异型的描述,但很罕见。SM的临床体征和症状源于MC释放过多介质,在侵袭性形式中,则源于与MC浸润相关的器官衰竭。因此,惰性SM的治疗主要旨在控制MC介质释放引起的症状。相比之下,在晚期SM中,如侵袭性SM、MC白血病和MC肉瘤,则必须考虑进行强化(化疗)治疗(无论是否进行异基因干细胞移植)。此外,大多数SM患者中发现有KIT激活突变(成人中大多为KIT D816V),因此目前正在开发旨在阻断突变KIT变体或/和下游信号通路的靶向疗法。其他靶点,如肿瘤性MC上表达的特定表面抗原,可能会被考虑用于晚期SM未来治疗的开发。

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