Noujaim Jonathan, Thway Khin, Bajwa Zia, Bajwa Ayeza, Maki Robert G, Jones Robin L, Keller Charles
Royal Marsden Hospital , London , UK.
Children's Cancer Therapy Development Institute , Fort Collins, CO , USA.
Front Oncol. 2015 Aug 17;5:186. doi: 10.3389/fonc.2015.00186. eCollection 2015.
Epithelioid sarcoma (ES) is a soft tissue sarcoma of children and young adults for which the preferred treatment for localized disease is wide surgical resection. Medical management is to a great extent undefined, and therefore for patients with regional and distal metastases, the development of targeted therapies is greatly desired. In this review, we will summarize clinically relevant biomarkers (e.g., SMARCB1, CA125, dysadherin, and others) with respect to targeted therapeutic opportunities. We will also examine the role of EGFR, mTOR, and polykinase inhibitors (e.g., sunitinib) in the management of local and disseminated disease. Toward building a consortium of pharmaceutical, academic, and non-profit collaborators, we will discuss the state of resources for investigating ES with respect to cell line resources, tissue banks, and registries so that a roadmap can be developed toward effective biology-driven therapies.
上皮样肉瘤(ES)是儿童和年轻人的一种软组织肉瘤,对于局限性疾病,首选治疗方法是广泛手术切除。医学管理在很大程度上尚不明确,因此对于有区域和远处转移的患者,非常需要开发靶向治疗方法。在本综述中,我们将总结与靶向治疗机会相关的临床相关生物标志物(如SMARCB1、CA125、失粘连蛋白等)。我们还将研究表皮生长因子受体(EGFR)、雷帕霉素靶蛋白(mTOR)和多激酶抑制剂(如舒尼替尼)在局部和播散性疾病管理中的作用。为了建立一个由制药公司、学术机构和非营利组织组成的合作联盟,我们将讨论在细胞系资源、组织库和登记处等方面研究ES的资源状况,以便制定一条通向有效生物学驱动疗法的路线图。