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骨肉瘤、软骨肉瘤和尤因肉瘤:国家癌症数据库报告。

Osteosarcoma, chondrosarcoma, and Ewing's sarcoma: National Cancer Data Base Report.

作者信息

Damron Timothy A, Ward William G, Stewart Andrew

机构信息

Musculoskeletal Sciences Research Laboratories, Department of Orthopedics, Syracuse, NY, USA.

出版信息

Clin Orthop Relat Res. 2007 Jun;459:40-7. doi: 10.1097/BLO.0b013e318059b8c9.

Abstract

We summarize descriptive epidemiologic and survival data from the National Cancer Data Base of the American College of Surgeons for 26,437 cases of osteosarcoma (n = 11,961), chondrosarcoma (n = 9606), and Ewing's sarcoma (n = 4870) from 1985 to 2003. Survival data are reported on cases with a minimum 5-year followup from 1985 to 1998 (8,104 osteosarcomas, 6,476 chondrosarcomas, and 3,225 Ewing's sarcomas). The relative 5-year survival rate was 53.9% for osteosarcoma, 75.2% for chondrosarcoma, and 50.6% for Ewing's sarcoma. Survival rates did not change notably over the collection period. Within osteosarcomas, the relative 5-year survival rates were 52.6% for high grade, 85.9% for parosteal, and 17.8% for Paget's subtypes. For osteosarcoma patients, the relative 5-year survival rate was 60% for those younger than 30 years, 50% for those aged 30 to 49 years, and 30% for those aged 50 years or older. Within chondrosarcomas, the relative 5-year survival rate was 76% for conventional, 71% for myxoid, 87% for juxtacortical, and 52% for mesenchymal. While the National Cancer Data Base has limitations, the survival data and demographics for bone sarcomas are unprecedented in numbers and duration. Our report supports continued efforts to refine data collection and stimulate further data analysis.

摘要

我们总结了美国外科医师学会国家癌症数据库中1985年至2003年期间26437例骨肉瘤(n = 11961)、软骨肉瘤(n = 9606)和尤因肉瘤(n = 4870)的描述性流行病学和生存数据。生存数据报告的是1985年至1998年至少随访5年的病例(8104例骨肉瘤、6476例软骨肉瘤和3225例尤因肉瘤)。骨肉瘤的5年相对生存率为53.9%,软骨肉瘤为75.2%,尤因肉瘤为50.6%。在收集期内生存率没有显著变化。在骨肉瘤中,高级别5年相对生存率为52.6%,骨膜下型为85.9%,佩吉特亚型为17.8%。对于骨肉瘤患者,年龄小于30岁者5年相对生存率为60%,30至49岁者为50%,50岁及以上者为30%。在软骨肉瘤中,传统型5年相对生存率为76%,黏液型为71%,皮质旁型为87%,间充质型为52%。虽然国家癌症数据库有局限性,但骨肉瘤的生存数据和人口统计学数据在数量和持续时间上都是前所未有的。我们的报告支持继续努力完善数据收集并促进进一步的数据分析。

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