Primary chordomas of the cervical spine: a consecutive series of 14 surgically managed cases.

OBJECT Cervical chordomas are rare lesions and usually bring about challenges in treatment planning because of their wide extension and complicated adjacent anatomy. There are few large published series at present focusing on cervical chordomas. The authors studied a consecutive series of 14 patients with primary cervical chordomas who underwent surgical treatment and were observed between 1989 and 2008. By reviewing the clinical patterns and follow-up data, they sought to investigate the clinical characters, tailor the appropriate surgical techniques, and establish prognosis factors for cervical chordomas. METHODS Hospitalization and follow-up data in the 14 patients were collected. All patients underwent piecemeal tumor excision and reconstruction for stability; total spondylectomy was achieved in 5 cases. Postoperative radiotherapy was administered in all patients. Kaplan-Meier plots were used to represent tumor recurrence and patient survival, and log-rank testing was used to determine the risk factors of local recurrence. RESULTS Follow-up ranged from 8 to 120 months (mean 58.6 months). Symptom and neural status in most patients improved after surgery. The 1- and 5-year disease-free survival rates were 78.6% and 50%, respectively, and the 1- and 5-year survival rates were 92.9% and 85.7%, respectively. Log-rank tests revealed that the following variables were significantly associated with a high rate of tumor recurrence: age less than 40 years or greater than 70 years (p = 0.006) and an upper cervical tumor location (p = 0.019). CONCLUSIONS Chordomas in the cervical spine are usually neoplasms that exhibit insidious growth and a wide extension by the time of diagnosis. Radical intralesional debulking surgery and postoperative radiotherapy have been effective treatment. A limited application of en bloc tumor resection and the highly likely intraoperative intralesional tumor seeding may partially explain the high local recurrence rate, whereas the chance of distant metastases, fortunately, is very low. Most recurrence were documented within 3 years. Some specific surgical techniques should be emphasized to minimize tumor seeding. Patients with upper cervical chordomas, younger adults, and elderly adults have worse prognosis. For patients with chordoma extending to both the anterior and posterior spinal columns, total spondylectomy combined with piecemeal excision is recommended for a better prognosis.

[1]  J. Zell,et al.  Analysis of prognostic factors for patients with chordoma with use of the California Cancer Registry. , 2012, The Journal of bone and joint surgery. American volume.

[2]  T. Witham,et al.  En Bloc Resection of Cervical Chordomas: Comparing Outcomes to Tumor Position , 2011 .

[3]  R. Jena,et al.  Residual postoperative tumour volume predicts outcome after high-dose radiotherapy for chordoma and chondrosarcoma of the skull base and spine. , 2011, Clinical oncology (Royal College of Radiologists (Great Britain)).

[4]  Ziya L Gokaslan,et al.  Preoperative grading scale to predict survival in patients undergoing resection of malignant primary osseous spinal neoplasms. , 2011, The spine journal : official journal of the North American Spine Society.

[5]  A. Schoenfeld,et al.  Chordoma of the Mobile Spine: A 15-Year Experience at the Massachusetts General Hospital , 2010 .

[6]  Y. Toyama,et al.  Complicated Surgical Resection of Malignant Tumors in the Upper Cervical Spine After Failed Ion-Beam Radiation Therapy , 2010, Spine.

[7]  A. Folpe,et al.  Clinical and Histopathologic Features of Chordomas in Children and Young Adults , 2010, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

[8]  S. Scully,et al.  Surgery Significantly Improves Survival in Patients With Chordoma , 2010, Spine.

[9]  V. Deviren,et al.  En bloc resection of primary tumors of the cervical spine: report of two cases and systematic review of the literature. , 2009, The spine journal : official journal of the North American Spine Society.

[10]  J. Lesser,et al.  Surgical management of chordomas of the cervical spine. , 2007, Journal of neurosurgery. Spine.

[11]  R. Laing,et al.  High-dose radiotherapy in the management of chordoma and chondrosarcoma of the skull base and cervical spine: Part 1--Clinical outcomes. , 2007, Clinical oncology (Royal College of Radiologists (Great Britain)).

[12]  S. Shabat,et al.  En bloc resection of a C4 chordoma: surgical technique , 2007, European Spine Journal.

[13]  M. Zileli,et al.  Primary tumors of the cervical spine: a retrospective review of 35 surgically managed cases. , 2007, The spine journal : official journal of the North American Spine Society.

[14]  G. Nielsen,et al.  Base of Skull Chordomas in Children and Adolescents: A Clinicopathologic Study of 73 Cases , 2006, The American journal of surgical pathology.

[15]  C. Fisher,et al.  En bloc marginal excision of a multilevel cervical chordoma. Case report. , 2006, Journal of neurosurgery. Spine.

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

[17]  Dong Han Lee,et al.  Hypofractionated Stereotactic Radiation Therapy for Skull Base and Upper Cervical Chordoma and Chondrosarcoma: Preliminary Results , 2006, Stereotactic and Functional Neurosurgery.

[18]  W. Ball,et al.  Cranial chordomas in infancy and childhood. A report of two cases and review of the literature , 2005, Pediatric Radiology.

[19]  S. Seagren,et al.  Prognostic factors in the management of metastatic epidural spinal cord compression , 1980, Journal of Neuro-Oncology.

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

[21]  P. Eysel,et al.  Metastasizing chordoma of the lumbar spine , 2002, European Spine Journal.

[22]  Mark Soo Chordoma: Review of Clinicoradiological Features and Factors Affecting Survival , 2001, Australasian radiology.

[23]  T. Pigott,et al.  En bloc removal of the lower lumbar vertebral body for chordoma. Report of two cases. , 2001, Journal of neurosurgery.

[24]  J. Schramm,et al.  Tumour Surgery of the Upper Cervical Spine – A Retrospective Study of 13 Cases , 2001, Acta Neurochirurgica.

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

[26]  Y. Shimada,et al.  Total spondylectomy for primary tumor of the thoracolumbar spine , 2000, Spinal Cord.

[27]  G. Nielsen,et al.  Chondrosarcoma of the base of the skull: a clinicopathologic study of 200 cases with emphasis on its distinction from chordoma. , 1999, The American journal of surgical pathology.

[28]  H. Okajima,et al.  Sacral Chordoma in Early Childhood: Clinicopathological and Immunohistochemical Study , 1998, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

[29]  J N Weinstein,et al.  Primary Bone Tumors of the Spine: Terminology and Surgical Staging , 1997, Spine.

[30]  Y. Hoshino,et al.  A Report on the Safety of Unilateral Vertebral Artery Ligation During Cervical Spine Surgery , 1996, Spine.

[31]  J. Munzenrider,et al.  Base of skull and cervical spine chordomas in children treated by high-dose irradiation. , 1995, International journal of radiation oncology, biology, physics.

[32]  M. Wick,et al.  Chordoma in childhood and adolescence. A clinicopathologic analysis of 12 cases. , 1993, Archives of pathology & laboratory medicine.

[33]  M. Urie,et al.  Probable causes of recurrence in patients with chordoma and chondrosarcoma of the base of skull and cervical spine. , 1993, International journal of radiation oncology, biology, physics.

[34]  E. Laws,et al.  Chordoma of the mobile spine. A clinicopathologic analysis of 40 patients , 1993, Cancer.

[35]  D. Day,et al.  Metastasizing Chordoma in Early Childhood , 1987 .

[36]  D. Day,et al.  Metastasizing chordoma in early childhood: a pathological and immunohistochemical study with review of the literature. , 1987, Pediatric pathology.

[37]  C. P. Schwinn,et al.  Chordoma. A clinicopathologic study of metastasis. , 1979, American journal of clinical pathology.

[38]  N. Sundaresan,et al.  Spinal chordomas. , 1979, Journal of neurosurgery.

[39]  J. Lin,et al.  Chordoma: radiologic evaluation of 20 cases. , 1976, AJR. American journal of roentgenology.

[40]  H. O. Hustu,et al.  Chordoma. Thirty‐five‐year study at memorial hospital , 1967, Cancer.