Harrison Douglas J, Geller David S, Gill Jonathan D, Lewis Valerae O, Gorlick Richard
a Department of Pediatrics , The University of Texas MD Anderson Cancer Center , Houston , TX , USA.
b Montefiore Medical Center and the Children's Hospital at Montefiore , The University Hospital for Albert Einstein College of Medicine , Bronx , NY , USA.
Expert Rev Anticancer Ther. 2018 Jan;18(1):39-50. doi: 10.1080/14737140.2018.1413939. Epub 2017 Dec 14.
Current treatment of osteosarcoma includes surgical resection of all gross disease in conjunction with systemic chemotherapy to control micro-metastatic disease. This yields a 5-year event free survival (EFS) of approximately 70% for patients with localized osteosarcoma while patients with metastatic or recurrent disease fare poorly with overall survival rates of less than 20%. Areas covered: This review outlines the current and future approach towards the treatment of osteosarcoma. A literature search was performed utilizing PubMed. Several recent clinical trials are reviewed in detail, as is innovative research evaluating novel agents and surgical techniques which hold promise. Expert commentary: The outcome for patients with osteosarcoma has not changed in several decades. This plateau in survival rates highlights the need for a novel approach towards research. There remains a great deal of interest in utilizing the very high risk population of recurrent osteosarcoma patients to rapidly and sequentially evaluate novel agents to determine if any of these agents hold promise. Several phase II studies are ongoing or in development that offer hope based on intriguing preclinical data. Furthermore, initiatives in obtaining specimens to further explore the genetic and immunological profile behind osteosarcoma will be essential towards identifying novel pathways and targets to exploit.
骨肉瘤的当前治疗方法包括手术切除所有肉眼可见的病灶,并结合全身化疗以控制微转移病灶。对于局限性骨肉瘤患者,这可使5年无事件生存率(EFS)达到约70%,而转移性或复发性疾病患者的预后较差,总生存率低于20%。涵盖领域:本综述概述了骨肉瘤治疗的当前和未来方法。利用PubMed进行了文献检索。详细回顾了几项近期的临床试验,以及评估有前景的新型药物和手术技术的创新性研究。专家评论:骨肉瘤患者的治疗结果几十年来一直没有改变。生存率的这种停滞凸显了采用新研究方法的必要性。利用复发性骨肉瘤患者这一极高风险人群来快速、相继评估新型药物,以确定这些药物是否有前景,这仍然备受关注。正在进行或正在开展的几项II期研究基于有趣的临床前数据带来了希望。此外,获取标本以进一步探索骨肉瘤背后的基因和免疫特征的举措,对于识别新的途径和可利用的靶点至关重要。