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青少年和青年癌症患者:最新进展——骨肿瘤。

The adolescent and young adult with cancer: state of the art -- bone tumors.

机构信息

Department of Pediatrics, Section of Hematology-Oncology, Baylor College of Medicine, Texas Children's Cancer and Hematology Centers, 6701 Fannin Street, Suite 1510.00, Houston, TX 77030, USA.

出版信息

Curr Oncol Rep. 2013 Aug;15(4):296-307. doi: 10.1007/s11912-013-0321-9.

Abstract

Primary malignant bone tumors in the pediatric to young adult populations are relatively uncommon and account for about 6 % of all cancers in those less than 20 years old [1] and 3 % of all cancers in adolescents and young adults (AYA) within the age range of 15 to 29 years [2]. Osteosarcoma (OS) and Ewing's sarcoma (ES) comprise the majority of malignant bone tumors. The approach to treatment for both tumors consists of local control measures (surgery or radiation) as well as systemic therapy with high-dose chemotherapy. Despite earlier advances, there have been no substantial improvements in outcomes over the past several decades, particularly for patients with metastatic disease. This review summarizes the major advances in the treatment of OS and ES and the standard therapies available today, current active clinical trials, and areas of investigation into molecularly targeted therapies.

摘要

儿童和青年人群中的原发性骨恶性肿瘤相对少见,约占所有 20 岁以下人群癌症的 6%[1],占 15 至 29 岁青少年和年轻成人(AYA)癌症的 3%[2]。骨肉瘤(OS)和尤文肉瘤(ES)构成了大多数恶性骨肿瘤。这两种肿瘤的治疗方法包括局部控制措施(手术或放疗)以及大剂量化疗的全身治疗。尽管取得了早期进展,但在过去几十年中,治疗结果并没有实质性改善,特别是对于转移性疾病的患者。这篇综述总结了骨肉瘤和尤文肉瘤治疗方面的主要进展以及目前可用的标准疗法、当前正在进行的临床试验以及针对分子靶向治疗的研究领域。

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