Broadhead Matthew L, Clark Jonathan C M, Myers Damian E, Dass Crispin R, Choong Peter F M
Department of Orthopaedics, Department of Surgery, University of Melbourne, St. Vincent's Hospital, SVHM, L3, Daly Wing, 35 Victoria Parade, Fitzroy VIC 3065, Australia.
Sarcoma. 2011;2011:959248. doi: 10.1155/2011/959248. Epub 2011 Apr 13.
Osteosarcoma is the most common primary malignancy of bone. It arises in bone during periods of rapid growth and primarily affects adolescents and young adults. The 5-year survival rate for osteosarcoma is 60%-70%, with no significant improvements in prognosis since the advent of multiagent chemotherapy. Diagnosis, staging, and surgical management of osteosarcoma remain focused on our anatomical understanding of the disease. As our knowledge of the molecular pathogenesis of osteosarcoma expands, potential therapeutic targets are being identified. A comprehensive understanding of these mechanisms is essential if we are to improve the prognosis of patients with osteosarcoma through tumour-targeted therapies. This paper will outline the pathogenic mechanisms of osteosarcoma oncogenesis and progression and will discuss some of the more frontline translational studies performed to date in search of novel, safer, and more targeted drugs for disease management.
骨肉瘤是最常见的原发性骨恶性肿瘤。它在骨骼快速生长时期发生,主要影响青少年和年轻成年人。骨肉瘤的5年生存率为60%-70%,自多药化疗出现以来,预后没有显著改善。骨肉瘤的诊断、分期和外科治疗仍集中在我们对该疾病的解剖学认识上。随着我们对骨肉瘤分子发病机制的了解不断扩展,潜在的治疗靶点正在被确定。如果我们要通过肿瘤靶向治疗改善骨肉瘤患者的预后,全面了解这些机制至关重要。本文将概述骨肉瘤发生和进展的致病机制,并讨论迄今为止为寻找用于疾病管理的新型、更安全和更有针对性的药物而进行的一些前沿转化研究。