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多模式治疗躯干骨肉瘤:骨肉瘤协作研究组(COSS)的经验

Osteosarcoma of the trunk treated by multimodal therapy: experience of the Cooperative Osteosarcoma study group (COSS).

作者信息

Bielack S S, Wulff B, Delling G, Göbel U, Kotz R, Ritter J, Winkler K

机构信息

Department of Pediatric Hematology and Oncology, University Hospital, Hamburg, Germany.

出版信息

Med Pediatr Oncol. 1995 Jan;24(1):6-12. doi: 10.1002/mpo.2950240103.

Abstract

The case histories of all patients with osteosarcoma of the trunk entered into the consecutive studies COSS 80 through COSS 86 of the Cooperative German/Austrian Osteosarcoma Study Group (COSS) were analyzed in order to evaluate their clinical characteristics and the impact of modern neoadjuvant therapy on prognosis. They were compared to those of all patients with extremity osteosarcoma treated according to the same protocols. While tumors of the trunk comprised only 32 (4.8%) of 665 primary classical osteosarcomas, secondary osteosarcomas were much more likely to be located in bones of the axial skeleton (6 of 18, 33%). Patients with primary osteosarcoma of the axial skeleton were older (mean: 20.8 vs. 15.2 years, P < 0.01) and were more likely to present with metastases at diagnosis (34% vs 12%, P < 0.001) than those with primary extremity osteosarcoma. In contrast to extremity tumors, local surgical treatment failure was very common in osteosarcomas of the trunk. Complete tumor removal was achieved in less than half of all evaluable cases. The prognosis of eight patients with localized primary axial osteosarcoma and effective surgical local control was not inferior to that of 483 equally evaluable patients with extremity tumors. In conclusion, while secondary systemic spread of axial osteosarcoma may be avoided in patients treated with multiagent chemotherapy, successful treatment is often barred by primary metastatic disease and inability to control the local tumor site.

摘要

德国/奥地利骨肉瘤协作研究组(COSS)对COSS 80至COSS 86连续研究中纳入的所有躯干骨肉瘤患者的病历进行了分析,以评估其临床特征以及现代新辅助治疗对预后的影响。将这些患者与按照相同方案治疗的所有四肢骨肉瘤患者进行比较。虽然在665例原发性经典骨肉瘤中,躯干肿瘤仅占32例(4.8%),但继发性骨肉瘤更有可能位于中轴骨骼的骨中(18例中有6例,33%)。与原发性四肢骨肉瘤患者相比,原发性中轴骨骼骨肉瘤患者年龄更大(平均:20.8岁对15.2岁,P<0.01),且在诊断时更有可能出现转移(34%对12%,P<0.001)。与四肢肿瘤不同,躯干骨肉瘤的局部手术治疗失败非常常见。在所有可评估病例中,不到一半实现了肿瘤完全切除。8例局限性原发性中轴骨肉瘤且手术局部控制有效的患者的预后并不亚于483例同样可评估的四肢肿瘤患者。总之,虽然接受多药化疗的患者可能避免中轴骨肉瘤的继发性全身扩散,但成功治疗往往因原发性转移性疾病和无法控制局部肿瘤部位而受阻。

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