首页> 外文期刊>British Journal of Cancer >Patterns of care and survival for patients aged under 40 years with bone sarcoma in Britain, 1980|[ndash]|1994
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Patterns of care and survival for patients aged under 40 years with bone sarcoma in Britain, 1980|[ndash]|1994

机译:英国,1980年[ndash] | 1994年40岁以下骨肉瘤患者的护理和生存方式

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The purpose of the study was to calculate population-based survival rates for osteosarcoma (OS) and Ewing's sarcoma (ES) in Great Britain during 1980–1994, determine proportions of patients treated at specialist centres or entered in national and international clinical trials, and investigate effects of these factors on survival. Data on a population-based series of 1349 patients with OS and 849 with ES were compiled from regional and national cancer registries, UK Children's Cancer Study Group, regional bone tumour registries and clinical trials. Follow-up was through population registers. Survival was analysed by actuarial analysis with log-rank tests and by Cox's proportional hazards analysis. Five-year survival rates during 1980–1984, 1985–1989 and 1990–1994 were 42% (95% CI: 37, 46), 54% (95% CI: 50, 59) and 53% (95% CI: 48, 57), respectively, for OS and 31% (95% CI: 26, 37), 46% (95% CI: 40, 51) and 51% (95% CI: 45, 57) for ES. Proportions of patients treated at a supraregional bone tumour centre or a paediatric oncology centre in the three quinquennia were 36, 56 and 67% for OS and 41, 60 and 69% for ES. In 1983–1992, 48% of OS patients were entered in a national trial; for ES, 27% were entered in 1980–1986 and 54% in 1987–1994. Survival was similar for trial and nontrial patients with OS. For ES, trial patients had consistently higher 5-year survival than nontrial patients: 1980–1986, 42 vs 30%; 1987–1992, 59 vs 42%; 1993–1994, 54 vs 43%. During 1985–1994, patients with OS or ES whose main treatment centre was a nonteaching hospital had lower survival rates. In multivariate analyses of patients diagnosed during 1985–1994 that also included age, sex, primary site, surgical treatment centre, the results relating to main treatment centre for both OS and ES retained significance but the survival advantage of trial entry for ES became nonsignificant. For both OS and ES diagnosed since 1985, patients whose main treatment centre was a nonspecialist hospital had a lower survival rate.
机译:该研究的目的是计算1980-1994年英国基于骨肉瘤(OS)和尤因氏肉瘤(ES)的人群生存率,确定在专科中心接受治疗或参加国家和国际临床试验的患者比例,以及调查这些因素对生存的影响。从地区和国家癌症登记机构,英国儿童癌症研究小组,地区骨肿瘤登记机构和临床试验中收集了基于人群的1349例OS患者和849例ES患者的数据。后续行动是通过人口登记。通过对数秩检验和Cox比例风险分析进行精算分析来分析生存率。 1980–1984、1985–1989和1990–1994年期间的五年生存率分别为42%(95%CI:37、46),54%(95%CI:50、59)和53%(对于OS和95%CI(95%CI:26、37),95%CI:48、57),46%(95%CI:40、51)和51%(95%) CI:45、57)。在三个昆仑病患者中,在上区骨肿瘤中心或儿科肿瘤中心接受治疗的患者中OS的比例为36%,56%和67%,ES的比例为41%,60%和69%。在1983年至1992年间,有48%的OS患者进入了一项全国性试验。对于ES,1980-1986年输入27%,1987-1994年输入54%。试验性和非试验性OS患者的生存率相似。对于ES,试验患者的5年生存率始终高于非试验患者:1980-1986年,分别为42%和30%。 1987–1992年,59对42%; 1993年至1994年,分别是54%和43%。在1985-1994年间,以主要治疗中心为非教学医院的OS或ES患者的生存率较低。在对1985-1994年期间诊断出的患者的多变量分析中,还包括年龄,性别,主要部位,外科治疗中心,有关OS和ES的主要治疗中心的结果仍然具有重要意义,但尝试ES的生存优势并不显着。对于自1985年以来诊断的OS和ES,主要治疗中心为非专科医院的患者生存率较低。

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