Department of Orthopaedic Surgery, Harvard Medical School, Massachusetts General Hospital, Boston, MA 02114, USA.
Spine J. 2010 Aug;10(8):708-14. doi: 10.1016/j.spinee.2010.05.017.
Because of the low incidence, treatment recommendations for spinal osteosarcoma are guided by the results of small series and case reports. Many include patients who presented for treatment over the course of three to four decades.
The goal of this investigation was to report the treatments, results, and overall survivorship of 26 patients treated for osteosarcoma of the spine at a single institution.
Retrospective prognostic series (Level III evidence).
Twenty-six patients treated at a single center for osteosarcoma of the spine over a 26-year period.
Estimation of patient survival, local recurrence, and the presence of metastatic disease.
We performed a retrospective review of cases of osteosarcoma involving the spine treated at our institution between 1982 and 2008. Medical charts, radiology reports, pathology reports, and operative notes were reviewed for all patients. Available imaging studies were also reviewed. The log-rank test was used to compare baseline differences between groups. Survivorship analysis was performed using Kaplan-Meier methodology. The effect of Paget osteosarcoma, type of resection, presence of local recurrence, tumor size, surgical margins, and metastases on overall survival were also investigated using the log-rank test.
Twenty-six patients were included for review in this study. Twenty individuals were treated surgically, and 24 were treated with radiation with a mean dose of 62.2 Gy (range 20-84.7 Gy). Twenty-five patients received chemotherapy. Of those treated surgically, seven received en bloc resection. The median overall survival for all patients in our series was 29.5 months (standard error 14.7, 95% confidence interval 0.6-58). Local recurrence developed in 7 patients (27%), and metastasis occurred in 16 individuals (62%). Patients with Paget osteosarcoma had worse overall survival (p<.001).
Results presented here confirm a poor prognosis for patients with spinal osteosarcoma. Although combination therapies, including surgery, chemotherapy, and high-dose radiation, achieve adequate short-term survival, the 5-year mortality rate remains high.
由于发病率低,脊柱骨肉瘤的治疗建议是基于小系列和病例报告的结果。许多研究包括在三到四十年间接受治疗的患者。
本研究的目的是报告在单一机构接受治疗的 26 例脊柱骨肉瘤患者的治疗、结果和总体生存率。
回顾性预后系列(III 级证据)。
26 例在单一中心接受治疗的脊柱骨肉瘤患者,随访时间为 26 年。
患者生存、局部复发和转移性疾病的估计。
我们对 1982 年至 2008 年间在我院治疗的脊柱骨肉瘤病例进行了回顾性研究。对所有患者的病历、放射学报告、病理报告和手术记录进行了审查。还对可用的影像学研究进行了回顾。使用对数秩检验比较组间基线差异。使用 Kaplan-Meier 方法进行生存分析。还使用对数秩检验研究 Paget 骨肉瘤、切除类型、局部复发、肿瘤大小、手术切缘和转移对总生存率的影响。
本研究共纳入 26 例患者进行回顾性分析。20 例患者接受手术治疗,24 例患者接受放疗,平均剂量为 62.2 Gy(范围 20-84.7 Gy)。25 例患者接受化疗。在接受手术治疗的患者中,有 7 例接受了整块切除术。本研究所有患者的中位总生存期为 29.5 个月(标准误差 14.7,95%置信区间 0.6-58)。7 例(27%)患者出现局部复发,16 例(62%)患者出现转移。患有 Paget 骨肉瘤的患者总体生存率较差(p<.001)。
这里提出的结果证实了脊柱骨肉瘤患者的预后较差。尽管包括手术、化疗和高剂量放疗在内的联合治疗可以实现短期生存,但 5 年死亡率仍然很高。