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骨尤文肉瘤的预后因素:对欧洲多组合作尤文肉瘤研究组975例患者的分析

Prognostic factors in Ewing's tumor of bone: analysis of 975 patients from the European Intergroup Cooperative Ewing's Sarcoma Study Group.

作者信息

Cotterill S J, Ahrens S, Paulussen M, Jürgens H F, Voûte P A, Gadner H, Craft A W

机构信息

Institute of Child Health, University of Newcastle upon Tyne, United Kingdom.

出版信息

J Clin Oncol. 2000 Sep;18(17):3108-14. doi: 10.1200/JCO.2000.18.17.3108.

Abstract

PURPOSE

To further elaborate on prognostic factors for Ewing's sarcoma of bone and to document improvements in relapse-free survival (RFS) and trends in local therapy over the study period (1977 to 1993).

PATIENTS AND METHODS

A retrospective analysis was performed on a combined Gesellschaft Für Pädiatrische Onkologie und Hämatologie/Cooperative Ewing Sarcoma Study and United Kingdom Children's Cancer Study Group/Medical Research Council data set of 975 patients registered with the respective trial offices before the current collaborative European Intergroup Cooperative Ewing's Sarcoma Study trial. Both groups independently undertook studies with similar chemotherapy during the period.

RESULTS

The key adverse prognostic factor is metastases at diagnosis (5-year RFS, 22% of patients with metastases at diagnosis v 55% of patients without metastases at diagnosis; P: <.0001). For the group with metastases, there was a trend for better survival for those with lung involvement compared with those with bone metastases or a combination of lung and bone metastases (P: <.0001). In the group of patients with no metastases at diagnosis, multivariate analysis demonstrated that site (axial v other), age-group (< 15 v > or = 15 years), and period of diagnosis had significant influence on RFS (all P: <.005). RFS was superior in the period after 1985 compared with the period before 1985 for nonmetastatic patients (45% v 60%, respectively; P: <.0001) and for metastatic patients (16% v 30%, respectively; P: =.016). Patients who relapsed within 2 years of diagnosis had a less favorable prognosis than patients who relapsed later (5-year survival after relapse, 4% v 23%, respectively; P: <. 0001). There were other changes over the period; in particular, radiotherapy or amputation were more common in the period before 1986, whereas endoprosthetic surgery was widely used in the later period.

CONCLUSION

Survival and RFS improved over the period. Prognostic factors are metastases at diagnosis, primary site, and age.

摘要

目的

进一步阐述骨尤文肉瘤的预后因素,并记录无复发生存期(RFS)的改善情况以及研究期间(1977年至1993年)局部治疗的趋势。

患者与方法

对德国儿科肿瘤学与血液学学会/尤文肉瘤合作研究组以及英国儿童癌症研究组/医学研究理事会的联合数据集进行回顾性分析,该数据集包含975例在当前欧洲尤文肉瘤协作组合作试验之前已在各自试验办公室登记的患者。两组在此期间独立开展了采用相似化疗方案的研究。

结果

关键的不良预后因素是诊断时出现转移(5年RFS,诊断时出现转移的患者为22%,而诊断时未出现转移的患者为55%;P:<.0001)。对于出现转移的患者组,与骨转移或肺与骨转移并存的患者相比,肺转移患者的生存趋势更好(P:<.0001)。在诊断时未出现转移的患者组中,多因素分析表明部位(轴向与其他)、年龄组(<15岁与≥15岁)以及诊断时期对RFS有显著影响(所有P:<.005)。对于非转移性患者,1985年之后的时期RFS优于1985年之前的时期(分别为45%与60%;P:<.0001),对于转移性患者也是如此(分别为16%与30%;P:=.016)。诊断后2年内复发的患者预后比之后复发的患者更差(复发后的5年生存率分别为4%与23%;P:<.0001)。在此期间还有其他变化;特别是,1986年之前放疗或截肢更为常见,而后期广泛采用了人工关节置换手术。

结论

在此期间生存率和RFS有所改善。预后因素为诊断时的转移情况、原发部位和年龄。

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