An institutional review of clear cell chondrosarcoma

Clin Orthop Relat Res. 2005 Nov:440:209-12. doi: 10.1097/01.blo.0000174686.70003.e0.

Abstract

Clear cell chondrosarcoma is a rare bone neoplasm with a slow progressive clinical course and infrequent metastasis, but with a high local recurrence rate. We sought to ascertain the long-term outcome of patients with this neoplasm and to identify possible factors predicting survival. Sixteen patients with clear cell chondrosarcomas treated at one institution and who had long-term clinical followup were identified. All patients were treated by surgical resection of the tumor, which was classified as clear (> 2 mm) in 10 patients and marginal or intralesional in six patients. Three patients had local recurrence after a median of 1.7 years. Metastatic disease developed in four patients with a median time to diagnosis of 8.1 years. Ten-year overall survival of patients with clear cell chondrosarcomas was 89%, and disease-free survival was 68%. Patients with surgical resections comprising clear margins had longer disease-free survival compared with patients with marginal and intralesional tumors. Inadequate surgical resection of clear cell chondrosarcoma leads to risk of local recurrence and metastatic disease. The malignancy has a tendency to metastasize relatively late, therefore, followup of patients is necessary after the generally accepted 5-year period.

Level of evidence: Prognostic study, Level III (case control study). See the Guidelines for Authors for a complete description of levels of evidence.

MeSH terms

  • Adolescent
  • Adult
  • Bone Neoplasms / diagnostic imaging
  • Bone Neoplasms / mortality*
  • Bone Neoplasms / surgery
  • Chondrosarcoma / diagnostic imaging
  • Chondrosarcoma / mortality*
  • Chondrosarcoma / surgery
  • Disease-Free Survival
  • Female
  • Femoral Neoplasms
  • Humans
  • Humerus
  • Male
  • Middle Aged
  • Neoplasm Recurrence, Local
  • Radiography
  • Survival Analysis