Jiang Yunyun, Ludwig Joseph, Janku Filip
Department of Investigational Cancer Therapeutics (Phase I Clinical Trials Program), The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Department of Sarcoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Cancer Treat Rev. 2015 May;41(5):391-400. doi: 10.1016/j.ctrv.2015.03.008. Epub 2015 Mar 27.
The prognosis of adolescent and young adult patients battling metastatic Ewing sarcoma family of tumors (ESFT) remains less than 30% despite the development of systemic therapies. In the era of personalized medicine, novel molecular targets have been tested in preclinical or clinical settings in ESFT. In this review, we focus on early clinical and translational research that identified multiple molecular targets, including IGF-1R; mTOR; tyrosine kinase inhibitors; EWS-FLI1-related targets, and others. Overall, novel targeted therapies demonstrated modest efficacy; however pronounced and durable antineoplastic responses have been observed in small subsets of treated patients, for example with IGF-1R antibodies. Identifying outcome-predicting biomarkers and overcoming treatment resistance remain major challenges. Due to the rarity of ESFT, multi-institutional collaboration efforts of clinicians, basic and translational scientists are needed in order to understand biology of therapeutic response or resistance, which can lead to development of novel therapeutic methods and improved patient outcomes.
尽管已经开发出全身治疗方法,但患有转移性尤因肉瘤家族性肿瘤(ESFT)的青少年和年轻成年患者的预后仍低于30%。在个性化医疗时代,新型分子靶点已在ESFT的临床前或临床环境中进行了测试。在本综述中,我们重点关注早期临床和转化研究,这些研究确定了多个分子靶点,包括胰岛素样生长因子1受体(IGF-1R);哺乳动物雷帕霉素靶蛋白(mTOR);酪氨酸激酶抑制剂;EWS-FLI1相关靶点等。总体而言,新型靶向疗法显示出适度的疗效;然而,在一小部分接受治疗的患者中观察到了明显且持久的抗肿瘤反应,例如使用IGF-1R抗体的患者。识别预测预后的生物标志物和克服治疗耐药性仍然是主要挑战。由于ESFT罕见,需要临床医生、基础和转化科学家进行多机构合作,以了解治疗反应或耐药性的生物学机制,这可能会导致开发新的治疗方法并改善患者预后。