Suppr超能文献

青少年和成人扁平骨骨肉瘤

Osteosarcomas of flat bones in adolescents and adults.

作者信息

Duffaud F, Digue L, Baciuchka-Palmaro M, Volot F, Perles-Daniel C, Garbe L, Favre R

机构信息

Department of Medical Oncology, C.H.U. "La Timone," Marseille, France.

出版信息

Cancer. 2000 Jan 15;88(2):324-32. doi: 10.1002/(sici)1097-0142(20000115)88:2<324::aid-cncr12>3.0.co;2-e.

Abstract

BACKGROUND

Osteosarcomas typically are long bone tumors and rarely affect the flat bones of the axial or appendicular skeleton.

METHODS

The authors examined cases of high grade osteosarcoma of flat bones diagnosed at La Timone Adults University Hospital during a 16-year period.

RESULTS

Sixteen patients with flat bone osteosarcomas were treated between 1980-1997. The median age of the patients was 25 years, with a male-to-female ratio of 14:2. Common presenting symptoms were swelling, pain, or both. Primary therapy included resection (n = 11 patients: alone in 8 patients and with radiation therapy in 3 patients), radiation therapy (n = 2 patients), or no local treatment (n = 3 patients). All patients received polychemotherapy, 7 preoperatively and postoperatively and 9 in the adjuvant setting. The overall 5-year survival rate was 47.7%; the overall median survival was 39 months (range, 4-211 months). The adequate local control rate was 68.7%. The local recurrence rate in patients who benefited from local treatment was 54%. Significant adverse prognostic factors on survival included the presence of synchronous metastases (three patients), metastases at any time during the course of the disease (eight patients), and inadequate local control (five patients). The overriding predictor of survival appeared to be the presence of metastases. Local recurrence appeared to have no influence on survival. No patient with metastases was alive at 3 years, whereas patients without recurrence or with local recurrence alone had a 5-year survival rate of 100%. Because the majority of patients with flat bone osteosarcomas ultimately die of metastatic disease, intensive systematic polychemotherapy should be an important component of treating these tumors.

CONCLUSIONS

Based on the very encouraging results observed in the treatment of long bone osteosarcomas, the therapy for flat bone osteosarcomas should combine radical surgery with preoperative and postoperative adjuvant chemotherapy.

摘要

背景

骨肉瘤通常是长骨肿瘤,很少累及轴向或附属骨骼的扁骨。

方法

作者研究了在拉蒂莫内成人大学医院16年间诊断出的扁骨高级别骨肉瘤病例。

结果

1980年至1997年间,16例扁骨骨肉瘤患者接受了治疗。患者的中位年龄为25岁,男女比例为14:2。常见的首发症状是肿胀、疼痛或两者皆有。主要治疗方法包括手术切除(11例患者:8例单独手术,3例联合放射治疗)、放射治疗(2例患者)或不进行局部治疗(3例患者)。所有患者均接受了多药化疗,7例术前和术后化疗,9例辅助化疗。总体5年生存率为47.7%;总体中位生存期为39个月(范围为4至211个月)。充分的局部控制率为68.7%。从局部治疗中获益的患者局部复发率为54%。生存的显著不良预后因素包括同时存在转移(3例患者)、疾病过程中任何时候出现转移(8例患者)以及局部控制不足(5例患者)。生存的首要预测因素似乎是转移的存在。局部复发似乎对生存没有影响。没有转移的患者3年时均存活,而没有复发或仅局部复发的患者5年生存率为100%。由于大多数扁骨骨肉瘤患者最终死于转移性疾病,强化系统性多药化疗应是治疗这些肿瘤的重要组成部分。

结论

基于在长骨骨肉瘤治疗中观察到的非常令人鼓舞的结果,扁骨骨肉瘤的治疗应将根治性手术与术前和术后辅助化疗相结合。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验