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卡斯尔曼病:从基础机制到分子治疗学。

Castleman's disease: from basic mechanisms to molecular therapeutics.

机构信息

Department of Investigational Cancer Therapeutics (Phase I Clinical Trials Program), MD Anderson Cancer Center, Unit 455, P.O. Box 301402, Houston, Texas 77030, USA.

出版信息

Oncologist. 2011;16(4):497-511. doi: 10.1634/theoncologist.2010-0212. Epub 2011 Mar 25.

Abstract

Castleman's disease is a rare lymphoproliferative disorder in which there has been recent progress in elucidating underlying mechanisms with potential therapeutic implications. Unicentric Castleman's disease is an indolent condition that is often treated with local approaches. In contrast, patients with multicentric Castleman's disease (MCD) have a less favorable prognosis and require systemic treatment. Cytotoxic chemotherapy, with its attendant risk for toxicity, has been widely used to treat MCD, with variable efficacy. The discovery of putative etiologic factors and targets in MCD, particularly human herpes virus 8, CD20, and interleukin (IL)-6, has been translated into the use of rituximab and anti-IL-6-based therapy, as well as antiviral agents. In this article, we review the current state of the art of our understanding of Castleman's disease and its treatment and we provide insight into future treatment strategies based on disease biology.

摘要

血管滤泡性淋巴结增生症是一种罕见的淋巴组织增生性疾病,目前在阐明潜在发病机制方面取得了一定的进展,这些机制可能具有治疗意义。局灶型血管滤泡性淋巴结增生症是一种惰性疾病,通常采用局部治疗方法。相比之下,多中心型血管滤泡性淋巴结增生症(MCD)患者的预后较差,需要全身性治疗。细胞毒性化疗因其毒性而被广泛用于治疗 MCD,但疗效不一。在 MCD 中发现了潜在的病因和靶点,特别是人类疱疹病毒 8、CD20 和白细胞介素(IL)-6,这已经转化为利妥昔单抗和基于抗 IL-6 的治疗以及抗病毒药物的应用。本文回顾了目前对血管滤泡性淋巴结增生症及其治疗的理解,并基于疾病生物学提供了对未来治疗策略的见解。

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Castleman's disease: from basic mechanisms to molecular therapeutics.卡斯尔曼病:从基础机制到分子治疗学。
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