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20世纪儿童骨肉瘤的生存率。1933年至2004年的趋势。

Twentieth-century survival from osteosarcoma in childhood. Trends from 1933 to 2004.

作者信息

Foster L, Dall G F, Reid R, Wallace W H, Porter D E

机构信息

Department of Paediatric Oncology, University of Edinburgh, Royal Hospital for Sick Children, Sciennes Road, Edinburgh EH9 1LW, UK.

出版信息

J Bone Joint Surg Br. 2007 Sep;89(9):1234-8. doi: 10.1302/0301-620X.89B9.19255.

Abstract

We have reviewed the data from our regional Bone Tumour Registry on patients with osteosarcoma diagnosed between 1933 and 2004 in order to investigate the relationship between survival and changes in treatment. There were 184 patients with non-metastatic appendicular osteosarcoma diagnosed at the age of 18 or under. Survival was calculated using Kaplan-Meier curves, and multivariate analysis was performed using the Cox regression proportional hazards model. The five-year survival improved from 21% between 1933 and 1959, to 62% between 1990 and 1999. During this time, a multi-disciplinary organisation was gradually developed to manage treatment. The most significant variable affecting outcome was the date of diagnosis, with trends in improved survival mirroring the introduction of increasingly effective chemotherapy. Our experience suggests that the guidelines of the National Institute for Clinical Excellence on the minimum throughput of centres for treatment should be enforced flexibly in those that can demonstrate that their historical and contemporary results are comparable to those published nationally and internationally.

摘要

我们回顾了本地区骨肿瘤登记处1933年至2004年间确诊的骨肉瘤患者的数据,以研究生存率与治疗变化之间的关系。有184例18岁及以下诊断为非转移性四肢骨肉瘤的患者。使用Kaplan-Meier曲线计算生存率,并使用Cox回归比例风险模型进行多变量分析。五年生存率从1933年至1959年的21%提高到1990年至1999年的62%。在此期间,逐渐形成了一个多学科组织来管理治疗。影响预后的最显著变量是诊断日期,生存率提高的趋势反映了越来越有效的化疗方法的引入。我们的经验表明,对于那些能够证明其历史和当代结果与国内和国际发表的结果相当的中心,国家临床优化研究所关于治疗中心最低治疗量的指南应灵活执行。

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