Esiashvili Natia, Goodman Michael, Marcus Robert B
Department of Radiation Oncology, Emory University School of Medicine, Atlanta, GA 30322, USA.
J Pediatr Hematol Oncol. 2008 Jun;30(6):425-30. doi: 10.1097/MPH.0b013e31816e22f3.
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.
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.
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.
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。
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%。
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。