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高级别局限性肢体骨肉瘤的生存:来自三个欧洲骨肉瘤协作组随机对照试验的联合结果和预后因素。

Survival from high-grade localised extremity osteosarcoma: combined results and prognostic factors from three European Osteosarcoma Intergroup randomised controlled trials.

机构信息

Department of Oncology, University College Hospital, London, UK.

出版信息

Ann Oncol. 2012 Jun;23(6):1607-16. doi: 10.1093/annonc/mdr491. Epub 2011 Oct 19.

Abstract

BACKGROUND

Neoadjuvant chemotherapy improves outcome in osteosarcoma. Determination of optimum regimens for survival, toxicity and prognostic factors requires randomised controlled trials to be conducted.

PATIENTS AND METHODS

Between 1983 and 2002, the European Osteosarcoma Intergroup recruited 1067 patients with localised extremity osteosarcoma to three randomised controlled trials. Standard treatment in each was doxorubicin 75 mg/m(2) and cisplatin 100 mg/m(2). Comparators were addition of methotrexate (BO02/80831), a multidrug regimen (BO03/80861) and a dose-intense schedule (BO06/80931). Standard survival analysis methods were used to identify prognostic factors, temporal and other influences on outcome.

RESULTS

Five- and 10-year survival were 56% (95% confidence interval 53% to 59%) and 52%, respectively (49% to 55%), with no difference between trials or treatment arms. Median follow-up was 9.4 years. Age range was 3-40 years (median 15). Limb salvage was achieved in 69%. Five hundred and thirty-three patients received the standard arm, 79% completing treatment. Good histological response to preoperative chemotherapy, distal tumour location (all sites other than proximal humerus/femur) and female gender were associated with improved survival.

CONCLUSIONS

Localised osteosarcoma will be cured in 50% of patients with cisplatin and doxorubicin. Large randomised trials can be conducted in this rare cancer. Failure to improve survival over 20 years argues for concerted collaborative international efforts to identify and rapidly test new treatments.

摘要

背景

新辅助化疗可改善骨肉瘤的预后。为了确定生存、毒性和预后因素的最佳方案,需要进行随机对照试验。

患者和方法

1983 年至 2002 年期间,欧洲骨肉瘤协作组招募了 1067 例局部肢体骨肉瘤患者,将其随机分为三组进行试验。每组的标准治疗方案均为多柔比星 75mg/m2 和顺铂 100mg/m2。比较组为添加甲氨蝶呤(BO02/80831)、多药方案(BO03/80861)和剂量密集方案(BO06/80931)。采用标准生存分析方法确定预后因素、时间和其他因素对结果的影响。

结果

5 年和 10 年生存率分别为 56%(95%置信区间 53%至 59%)和 52%(49%至 55%),试验之间或治疗组之间无差异。中位随访时间为 9.4 年。年龄范围为 3-40 岁(中位数为 15 岁)。肢体保留率为 69%。533 例患者接受标准治疗,其中 79%完成了治疗。术前化疗的良好组织学反应、肿瘤位于远端(除肱骨/股骨近端外的所有部位)和女性均与生存改善相关。

结论

对于接受顺铂和多柔比星治疗的局部骨肉瘤患者,有 50%可以治愈。对于这种罕见的癌症,可以进行大型的随机试验。20 多年来,生存率没有提高,这表明需要协调一致的国际合作努力,以确定并迅速测试新的治疗方法。

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