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过去30年尤因肉瘤患者的发病率和生存率变化:监测、流行病学与最终结果数据

Changes in incidence and survival of Ewing sarcoma patients over the past 3 decades: Surveillance Epidemiology and End Results data.

作者信息

Esiashvili Natia, Goodman Michael, Marcus Robert B

机构信息

Department of Radiation Oncology, Emory University School of Medicine, Atlanta, GA 30322, USA.

出版信息

J Pediatr Hematol Oncol. 2008 Jun;30(6):425-30. doi: 10.1097/MPH.0b013e31816e22f3.

Abstract

PURPOSE

The US population-based cancer registry Surveillance, Epidemiology, and End Results (SEER) database provides an opportunity to evaluate the incidence and survival rates of Ewing sarcoma (ES) for the past 3 decades. This analysis reflects trends for the diagnosis of localized versus metastatic disease and changes in ES survival in a setting of wide-ranging cancer care institutions across the United States, which is expected to be different from clinical trials published to date.

MATERIALS/METHODS: Data from the SEER public-access database were reviewed for the diagnosis of ES of the bone among patients of 1 to 19 years of age between 1973 and 2004. Age-adjusted incidence was analyzed for the entire group and for localized and metastatic disease separately over the past 3 decades. Actuarial survival rates were examined for 3 intervals: 1973 to 1982, 1983 to 1992, and 1993 to 2004.

RESULTS

The overall incidence of ES seemed to remain unchanged with an average of 2.93 cases/1,000,000 reported annually between 1973 and 2004. The proportion of patients with distant metastasis among all ES cases remained in the 26% to 28% range, whereas the percent of localized cases slightly increased from 57% in 1973 to 1982 to 67% in 1993 to 2004 and the proportion of unstaged cases decreased from 17% to 5%. The 5-year survival of localized disease increased from 44% in the first study decade to 68% in the period after 1993, whereas 5-year survival of metastatic disease increased from 16% to 39%. The corresponding 10-year survival increased from 39% to 63% for localized disease and from 16% to 32% for metastatic ES.

CONCLUSIONS

The incidence of ES has not increased appreciably over the last 30 years. A marked decrease in the proportion of unstaged cases may be reflective of diagnostic improvement or changes in reporting. There is a clear improvement in survival for both localized and metastatic disease. Poorer outcome of metastatic patients still warrants intensification of therapy, which is currently being tested in several ongoing trials.

摘要

目的

基于美国人群的癌症登记系统监测、流行病学和最终结果(SEER)数据库提供了一个机会,可用于评估过去30年中尤因肉瘤(ES)的发病率和生存率。该分析反映了局限性疾病与转移性疾病的诊断趋势,以及在美国广泛的癌症治疗机构环境中ES生存率的变化,预计这与迄今发表的临床试验情况不同。

材料/方法:回顾SEER公共访问数据库中1973年至2004年间1至19岁患者骨ES诊断的数据。分析了过去30年中整个组以及局限性和转移性疾病的年龄调整发病率。检查了三个时间段的精算生存率:1973年至1982年、1983年至1992年和1993年至2004年。

结果

ES的总体发病率似乎保持不变,1973年至2004年间每年报告的平均发病率为2.93例/100万。所有ES病例中远处转移患者的比例保持在26%至28%之间,而局限性病例的百分比从1973年至1982年的57%略有增加至1993年至2004年的67%,未分期病例的比例从17%降至5%。局限性疾病的5年生存率从第一个研究十年的44%增加到1993年后时期的68%,而转移性疾病的5年生存率从16%增加到39%。局限性疾病相应的10年生存率从39%增加到63%,转移性ES从16%增加到32%。

结论

在过去30年中,ES的发病率没有明显增加。未分期病例比例的显著下降可能反映了诊断的改善或报告的变化。局限性和转移性疾病的生存率均有明显改善。转移性患者较差的预后仍需要强化治疗,目前正在多项正在进行的试验中进行测试。

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