Chondrosarcoma of the Mobile Spine

软骨肉瘤 医学 骨盆 阑尾骨 外科 回顾性队列研究 骶骨 解剖
作者
Daniel G. Tobert,Sidney Messier,Andrew J. Schoenfeld,Chinmay V. Bakshi,Shannon M. MacDonald,Joseph H. Schwab
出处
期刊:Spine [Lippincott Williams & Wilkins]
被引量:1
标识
DOI:10.1097/brs.0000000000005023
摘要

Study Design. Retrospective study. Objective. The objective is to report the clinical data for patients treated with mobile spine chondrosarcoma. Summary of Background Data. Chondrosarcoma of the mobile spine is a rare and challenging entity. A handful of case series have been published that report the clinical results of treatment, largely influenced by chondrosarcoma of the appendicular skeleton and pelvis. The clinical results of patients treated for chondrosarcoma of the mobile spine from our institution were published over ten years ago and this represents and update since that publication. Methods. Inclusion criteria were adults patients treated for chondrosarcoma of the mobile spine at Massachusetts General Hospital between 2007-2020. Patients with large sacral tumors extending into the lumbar spine were excluded. Further, we excluded patients with metastatic chondrosarcoma undergoing palliative decompressions for neurologic instability or instrumented procedures for biomechanical instability. Therefore, only patients undergoing definitive surgery at the primary site of disease in the mobile spine were included. Results. Twenty-four patients were included for review in this series. Seventeen of the 24 patients had their tumors excised with negative (R0) margins. Three of these 17 patients (18%) were dead of disease at final follow-up. There were two patients with R1 resections and five patients with R2 resections. Three of the 7 patients (43%) with positive margins were dead of disease at final follow-up. A Cox proportional hazard analysis indicated total radiation dose was a significant covariate (HR 1.18, 95% CI 1.01 - 1.39, P =0.03). Conclusion. We found higher percentages of overall survival with R0 tumor resection and lower histologic grade whereas development of metastatic disease was closely associated with local recurrence and poor survival. Despite the improvements in treatment paradigms, it is sobering that our findings largely mirror those of previous work considering patients treated between 1984 and 2006.
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