National AIDS Center, Istituto Superiore di Sanità, Viale Regina Elena 299, 00161 Rome, Italy.
Expert Opin Pharmacother. 2011 Aug;12(11):1669-90. doi: 10.1517/14656566.2011.577066. Epub 2011 Apr 25.
Kaposi's sarcoma (KS) is an angioproliferative disease that occurs in four clinical-epidemiological forms sharing the same immunological and histopathological features, suggesting common etiological and pathogenic factors. Infection with the human herpesvirus 8, cytokine- and angiogenic factor-induced growth together with an immuno-dysregulated state represent fundamental conditions for the development of this tumor. Despite the recent improvements in KS management, it remains an incurable disease.
The growing knowledge of KS biology provides multiple opportunities for the development of rational, molecularly targeted therapies. The present review summarizes the current management of KS, including local and systemic conventional therapies, and thoroughly describes the results obtained with new pathogenesis-based anti-KS treatments.
Kaposi's sarcoma represents a paradigm of how the elucidation of disease pathogenesis can drive the development of molecularly targeted treatments. The multifactorial pathogenesis of KS has led to the evaluation of many experimental agents targeting one or more specific factors or pathways involved in the development or progression of the disease. Although targeted therapy so far represents investigational treatment, clinical evaluation of several of these agents is yielding promising results.
卡波氏肉瘤(KS)是一种血管增生性疾病,有四种临床流行病学形式,具有相同的免疫和组织病理学特征,提示存在共同的病因和发病因素。人类疱疹病毒 8 感染、细胞因子和血管生成因子诱导的生长以及免疫失调状态是这种肿瘤发生的基本条件。尽管 KS 的治疗最近有所改善,但它仍然是一种无法治愈的疾病。
对 KS 生物学的日益了解为开发合理的、针对分子靶点的治疗方法提供了多种机会。本综述总结了 KS 的当前治疗方法,包括局部和全身常规治疗,并详细描述了基于新发病机制的抗 KS 治疗的结果。
卡波氏肉瘤代表了一种范例,即阐明疾病发病机制如何能够推动针对分子靶点的治疗方法的发展。KS 的多因素发病机制导致了对许多针对疾病发展或进展中涉及的一个或多个特定因素或途径的实验性药物的评估。尽管靶向治疗目前代表了研究性治疗,但对这些药物中的几种进行临床评估正在产生有希望的结果。