Ross Keir A, Smyth Niall A, Murawski Christopher D, Kennedy John G
Hospital for Special Surgery, 523 East 72nd Street, Suite 507, New York, NY 10021, USA.
ISRN Oncol. 2013;2013:759725. doi: 10.1155/2013/759725. Epub 2013 Jan 10.
Objective. The goal of this study was to review the current literature on the biology of Ewing's sarcoma, including current treatments and the means by which an understanding of biological mechanisms could impact future treatments. Methods. A search of PubMed and The Cochrane Collaboration was performed. Both preclinical and clinical evidence was considered, but specific case reports were not. Primary research articles and reviews were analyzed with an emphasis on recent publications. Results. Ewing sarcoma is associated with specific chromosomal translocations and the resulting transcripts/proteins. Knowledge of the biology of Ewing sarcoma has been growing but has yet to significantly impact or produce new treatments. Localized cases have seen improvements in survival rates, but the same cannot be said of metastatic and recurrent cases. Standard surgical, radiation, and chemotherapy treatments are reaching their efficacy limits. Conclusion. Improving prognosis likely lies in advancing biomarkers and early diagnosis, determining a cell(s) of origin, and developing effective molecular therapeutics and antiangiogenic agents. Preclinical evidence suggests the utility of molecular therapies for Ewing sarcoma. Early clinical results also reveal potential for novel treatments but require further development and evaluation before widespread use can be advocated.
目的。本研究的目的是回顾目前关于尤因肉瘤生物学的文献,包括当前的治疗方法以及对生物学机制的理解可能影响未来治疗的方式。方法。对PubMed和考科蓝协作网进行了检索。同时考虑了临床前和临床证据,但不包括具体的病例报告。对主要研究文章和综述进行了分析,重点是近期的出版物。结果。尤因肉瘤与特定的染色体易位以及由此产生的转录本/蛋白质有关。对尤因肉瘤生物学的认识一直在增加,但尚未对治疗产生显著影响或带来新的治疗方法。局限性病例的生存率有所提高,但转移性和复发性病例并非如此。标准的手术、放疗和化疗治疗正接近其疗效极限。结论。改善预后可能在于推进生物标志物和早期诊断、确定起源细胞以及开发有效的分子疗法和抗血管生成药物。临床前证据表明分子疗法对尤因肉瘤有用。早期临床结果也显示了新治疗方法的潜力,但在广泛应用之前需要进一步开发和评估。