Department of Neurosurgery, Cedars-Sinai Medical Center, Los Angeles, CA 90048, USA.
Eur Spine J. 2013 Jun;22(6):1375-82. doi: 10.1007/s00586-012-2621-4. Epub 2012 Dec 21.
Malignant osseous spinal neoplasms are aggressive tumors associated with poor outcomes despite aggressive multidisciplinary measures. While surgical resection has been shown to improve short-term local disease control, it remains debated whether surgical resection is associated with improved overall survival in patients with malignant primary osseous spinal neoplasms. The aim of this manuscript is to review survival data from a US cancer registry spanning 30 years to determine if surgical resection was independently associated with overall survival.
The SEER registry (1973-2003) was queried to identify cases of histologically confirmed primary spinal chordoma, chondrosarcoma, osteosarcoma, or Ewing's sarcoma of the mobile spine and pelvis. Patients with systemic metastasis were excluded. Age, gender, race, tumor location, and primary treatments were identified. Extent of local tumor invasion was classified as confined within periosteum versus extension beyond periosteum to surrounding tissues. The association of surgical resection with overall survival was assessed via Cox analysis adjusting for age, radiotherapy, and tumor invasiveness.
827 patients were identified with non-metastatic primary osseous spinal neoplasms (215 chordoma, 282 chondrosarcoma, 158 osteosarcoma, 172 Ewing's sarcoma). Overall, median survival was histology specific (chordoma, 96 months; Ewing's sarcoma, 90 months; chondrosarcoma, 88 months; osteosarcoma, 18 months). Adjusting for age, radiation therapy, and extent of local tumor invasion in patients with isolated (non-metastatic) spine tumors, surgical resection was independently associated with significantly improved survival for chordoma [hazard ratio (95 % confidence interval; 0.617 (0.25-0.98)], chondrosarcoma [HR (95 %CI); 0.153 (0.07-0.36)], osteosarcoma [HR (95 %CI); 0.382 (0.21-0.69)], and Ewing's sarcoma [HR (95 %CI); 0.494 (0.26-0.96)].
In our analysis of a 30-year US population-based cancer registry (SEER), patients undergoing surgical resection of primary spinal chordoma, chondrosarcoma, Ewing's sarcoma, or osteosarcoma demonstrated prolonged overall survival independent of patient age, extent of local invasion, or location. Surgical resection may play a role in prolonging survival in the multi-modality treatment of patients with these malignant primary osseous spinal neoplasms.
恶性骨脊柱肿瘤是一种侵袭性肿瘤,尽管采取了积极的多学科措施,但其预后仍较差。虽然手术切除已被证明可以改善短期局部疾病控制,但对于恶性原发性骨脊柱肿瘤患者,手术切除是否与总体生存率的提高相关仍存在争议。本文旨在回顾美国癌症登记处 30 年来的生存数据,以确定手术切除是否与总体生存率独立相关。
通过 SEER 登记处(1973-2003 年)查询组织学证实的原发性脊柱脊索瘤、软骨肉瘤、骨肉瘤或尤因肉瘤的病例,排除有全身转移的患者。确定患者的年龄、性别、种族、肿瘤位置和主要治疗方法。局部肿瘤侵犯程度分为局限于骨膜内与超出骨膜侵犯周围组织。通过 Cox 分析评估手术切除与总生存的相关性,调整年龄、放疗和肿瘤侵袭性因素。
共确定了 827 例非转移性原发性骨脊柱肿瘤患者(215 例脊索瘤、282 例软骨肉瘤、158 例骨肉瘤、172 例尤文肉瘤)。总体而言,中位生存时间因组织学而异(脊索瘤为 96 个月,尤文肉瘤为 90 个月,软骨肉瘤为 88 个月,骨肉瘤为 18 个月)。在仅患有脊柱肿瘤(无转移)的患者中,根据年龄、放疗和局部肿瘤侵犯程度进行调整后,手术切除与脊索瘤[风险比(95%置信区间):0.617(0.25-0.98)]、软骨肉瘤[HR(95%CI):0.153(0.07-0.36)]、骨肉瘤[HR(95%CI):0.382(0.21-0.69)]和尤文肉瘤[HR(95%CI):0.494(0.26-0.96)]的生存率显著提高独立相关。
在对 30 年美国人群癌症登记处(SEER)的分析中,接受原发性脊柱脊索瘤、软骨肉瘤、尤文肉瘤或骨肉瘤手术切除的患者,其总体生存率延长,与患者年龄、局部侵犯程度或肿瘤位置无关。手术切除可能在这些恶性原发性骨脊柱肿瘤的多模式治疗中延长患者的生存时间。