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儿童骨肉瘤的生物学与治疗进展

Biology and therapeutic advances for pediatric osteosarcoma.

作者信息

Marina Neyssa, Gebhardt Mark, Teot Lisa, Gorlick Richard

机构信息

Department of Pediatrics, Division of Hematology-Oncology, Stanford University Medical Center, Stanford, California 94305-5208, USA.

出版信息

Oncologist. 2004;9(4):422-41. doi: 10.1634/theoncologist.9-4-422.

Abstract

Osteosarcoma is the most common malignant bone tumor in children and adolescents. Survival for these patients was poor with the use of surgery and/or radiotherapy. The introduction of multi-agent chemotherapy dramatically improved the outcome for these patients and the majority of modern series report 3-year disease-free survival of 60%-70%. This paper describes current strategies for treating patients with osteosarcoma as well as review of the clinical features, radiologic and diagnostic work-up, and pathology. The authors review the state of the art management for patients with osteosarcoma in North America and Europe including the use of limb-salvage procedures and reconstruction as well as discuss the etiologic and biologic factors associated with tumor development. Therapy-related sequelae and future directions in the biology and therapy for these patients are also discussed.

摘要

骨肉瘤是儿童和青少年中最常见的恶性骨肿瘤。使用手术和/或放疗治疗这些患者的生存率很低。多药化疗的引入显著改善了这些患者的治疗结果,大多数现代研究系列报告3年无病生存率为60%-70%。本文描述了目前治疗骨肉瘤患者的策略,并对临床特征、放射学和诊断检查以及病理学进行了综述。作者回顾了北美和欧洲骨肉瘤患者的最新治疗方法,包括保肢手术和重建的应用,并讨论了与肿瘤发生相关的病因和生物学因素。还讨论了这些患者的治疗相关后遗症以及生物学和治疗的未来方向。

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