Preoperative grading scale to predict survival in patients undergoing resection of malignant primary osseous spinal neoplasms.

BACKGROUND CONTEXT Large population-based studies of malignant primary osseous spinal neoplasms are lacking and are necessary to have sufficient statistical power to determine if various patient-related factors are in fact significant indicators of prognosis. PURPOSE Using a 30-year US national cancer registry (Surveillance, Epidemiology, and End Results [SEER]), we introduce a preoperative grading scale that is associated with survival in patients undergoing surgical resection for malignant primary osseous spinal neoplasms. STUDY DESIGN Large-scale retrospective study. PATIENT SAMPLE SEER registry. OUTCOME MEASURE Survival. METHODS The SEER registry (1973-2003) was queried to identify adult patients undergoing surgical resection of histologically confirmed primary spinal chordoma, chondrosarcoma, or osteosarcoma via International Classification of Disease for Oncology, Third Edition coding. Variables independently associated with survival were determined via Cox proportional hazards regression analysis for all tumor types. A grading scale comprising these independent survival predictors was then developed and applied to each histology-specific tumor cohort. RESULTS Three hundred forty-two patients who underwent surgical resection of a malignant primary osseous spinal neoplasm (114 chordoma, 156 chondrosarcoma, and 72 osteosarcoma) were identified. Overall median survival after surgical resection was histology specific (osteosarcoma: 22 months; chordoma: 100 months; and chondrosarcoma: 160 months). Increasing age (years) and increasing tumor invasion (confined to periosteum; invasion through periosteum into adjacent tissues; and distal site metastasis) were the only variables independently associated with decreased survival (p<.05) for all tumor types. For spinal chordoma, sacrum/pelvic location (p<.05) and earlier year of surgery (p<.005) were also independently associated with decreased survival. Using variables of patient age, extent of local tumor invasion, and metastasis status in a five-point grading scale, increasing score (1-5) closely correlated (p<.001) with decreased survival for chordoma, chondrosarcoma, and osteosarcoma. CONCLUSIONS In our analysis of a US population-based cancer registry (SEER), a grading scale consisting of age, metastasis status, and extent of local tumor invasion was associated with overall survival after surgical resection of chordoma, chondrosarcoma, and osteosarcoma of the spine. Although this analysis could not take into account specific chemotherapy regimens and variations in surgical technique, this grading scale may offer valuable prognostic data based on variables available to the surgeon and patient before surgery and may help guide level of aggressiveness in subsequent treatment strategies.

[1]  P. Picci,et al.  Chondrosarcoma of the mobile spine: report on 22 cases. , 2000, Spine.

[2]  J. Lin,et al.  The osseous and angiographic features of vertebral chordomas , 1975, Neuroradiology.

[3]  G. Fuller,et al.  Expression and role of matrix metalloproteinases MMP-2 and MMP-9 in human spinal column tumors , 1998, Clinical & Experimental Metastasis.

[4]  D. Chang,et al.  Predictors of Inpatient Death and Complications among Postoperative Elderly Patients with Metastatic Brain Tumors , 2011, Annals of Surgical Oncology.

[5]  G. Krol,et al.  Combined treatment of osteosarcoma of the spine. , 1988, Neurosurgery.

[6]  K. Unni,et al.  Chondrosarcoma of the spine. , 1989, The Journal of bone and joint surgery. American volume.

[7]  Z. Gokaslan,et al.  Multidisciplinary Management of Primary Tumors of the Vertebral Column , 2009, Current treatment options in oncology.

[8]  G. Fuller,et al.  Sacral chordoma: 40-year experience at a major cancer center. , 1999, Neurosurgery.

[9]  M Beth McCarville,et al.  Temozolomide and intravenous irinotecan for treatment of advanced Ewing sarcoma , 2007, Pediatric blood & cancer.

[10]  L. Kindblom,et al.  Prognostic factors and outcome of pelvic, sacral, and spinal chondrosarcomas , 2001, Cancer.

[11]  W. Winkelmann,et al.  Significance of surgical margin on the prognosis of patients with Ewing's sarcoma: A report from the Cooperative Ewing's Sarcoma Study , 1996, Cancer.

[12]  Ganesh Rao,et al.  Surgical management of primary and metastatic sarcoma of the mobile spine. , 2008, Journal of neurosurgery. Spine.

[13]  T. Ozaki,et al.  Secondary chondrosarcoma in osteochondromas. Medullary extension in 15 of 45 cases. , 1997, Acta orthopaedica Scandinavica.

[14]  M. Sundaram,et al.  Primary vertebral osteosarcoma: imaging findings. , 2004, Radiology.

[15]  Z. L. Gokaslan,et al.  Total en bloc lumbar spondylectomy. Case report. , 2001, Journal of neurosurgery.

[16]  F. Sim,et al.  Osteosarcoma of the spine. , 1986, The Journal of bone and joint surgery. American volume.

[17]  A. Goldstein,et al.  Chordoma: incidence and survival patterns in the United States, 1973–1995 , 2004, Cancer Causes & Control.

[18]  G. Rosen,et al.  Primary malignant tumors of the spine. , 2009, The Orthopedic clinics of North America.

[19]  Z. Gokaslan,et al.  Ewing and Osteogenic Sarcoma: Evidence for Multidisciplinary Management , 2009, Spine.

[20]  Ziya L Gokaslan,et al.  Long-Term Clinical Outcomes Following En Bloc Resections for Sacral Chordomas and Chondrosarcomas: A Series of Twenty Consecutive Patients , 2009, Spine.

[21]  W. Winkelmann,et al.  Sacral Infiltration in Pelvic Sarcomas: Joint Infiltration Analysis II , 2003, Clinical orthopaedics and related research.

[22]  W. Winkelmann,et al.  Osteosarcoma of the spine , 2002, Cancer.

[23]  G. Gallia,et al.  En bloc resection of primary sacral tumors: classification of surgical approaches and outcome. , 2005, Journal of neurosurgery. Spine.

[24]  A W Duncan,et al.  Chondrosarcoma of the Spine , 1978, Spine.

[25]  W. Winkelmann,et al.  Transarticular invasion of iliopelvic sarcomas into the sacrum. Radiological analysis of 47 cases. , 1997, Acta orthopaedica Scandinavica.

[26]  J. Weinstein,et al.  Chordoma of the Mobile Spine: Fifty Years of Experience , 2006, Spine.

[27]  R. Lorentzon,et al.  The incidence of malignant primary bone tumours in relation to age, sex and site. A study of osteogenic sarcoma, chondrosarcoma and Ewing's sarcoma diagnosed in Sweden from 1958 to 1968. , 1974, The Journal of bone and joint surgery. British volume.

[28]  C. H. Price,et al.  Incidence of bone sarcoma in SW England, 1946-74, in relation to age, sex, tumour site and histology. , 1977, British Journal of Cancer.

[29]  P. Casali,et al.  Response to imatinib plus sirolimus in advanced chordoma. , 2009, Annals of oncology : official journal of the European Society for Medical Oncology.

[30]  L. Kindblom,et al.  Prognostic factors in chordoma of the sacrum and mobile spine , 2000, Cancer.

[31]  Mark Hachey,et al.  A New Method of Estimating United States and State‐level Cancer Incidence Counts for the Current Calendar Year , 2007, CA: a cancer journal for clinicians.

[32]  A. Bencivenga,et al.  An epidemiological study of osteogenic sarcoma in Kenya , 1985, International Orthopaedics.

[33]  Z. L. Gokaslan,et al.  Total en bloc lumbar spondylectomy , 2001 .

[34]  D. Reede,et al.  Computed tomography of spinal chordomas. , 1986, The Journal of computed tomography.

[35]  A. Abioye,et al.  Primary malignant tumors of bone: incidence in Ibadan, Nigeria. , 1982, Journal of the National Medical Association.

[36]  R. Berk,et al.  Chondrosarcoma of the spine: 1954 to 1997. , 1999, Journal of neurosurgery.

[37]  M Beth McCarville,et al.  Combination of gemcitabine and docetaxel in the treatment of children and young adults with refractory bone sarcoma , 2008, Cancer.

[38]  P. Mccormick Sacral Chordoma: 40-Year Experience at a Major Cancer Center , 1999 .

[39]  S. Cannon,et al.  Sacral Chordoma: Can Local Recurrence After Sacrectomy Be Predicted? , 2008, Clinical orthopaedics and related research.

[40]  E. Transfeldt,et al.  Lumbosacral chordoma. Prognostic factors and treatment. , 1999, Spine.

[41]  Kiyoshi Saito,et al.  Long-term control of clival chordoma with initial aggressive surgical resection and gamma knife radiosurgery for recurrence , 2009, Acta Neurochirurgica.

[42]  U. Batzdorf Primary spinal syringomyelia. Invited submission from the joint section meeting on disorders of the spine and peripheral nerves, March 2005. , 2005, Journal of neurosurgery. Spine.