Secondary Malignancy in Giant Cell Tumor: A Single-Center Study

Curr Oncol. 2022 Jun 2;29(6):4068-4080. doi: 10.3390/curroncol29060324.

Abstract

Giant cell tumor of bone (GCTB) undergoes a sarcomatous transformation. Secondary malignancy in giant cell tumor (MGCT) is associated with radiotherapy and has a dismal prognosis. We reviewed medical records to investigate the clinicopathological characteristics and prognosis of MGCT patients. The enrollment criterion was high-grade spindle-cell sarcoma, which developed at the site of prior GCTB treatment. Twelve patients were analyzed: six females and six males. The median age was 42.5 years. Benign recurrence occurred in five GCTB patients not treated with radiotherapy. No pulmonary implants were observed. The median latency to the malignant transformation was 63 months. Nine patients were AJCC stage IIB, and three were stage IVA. The median follow-up period after malignant transformation was 62.5 months. Five patients developed local recurrence, and six had distant metastasis. Five-year overall recurrence and metastasis-free survival rates were 61.9%, 66.7%, and 58.3%, respectively. Initial metastasis was a predictive factor for overall survival. Benign local recurrence of GCTB was also a negative factor for metastasis-free survival of MGCT patients. Differences in overall survival according to benign recurrence also showed a tendency toward significance. In our series, secondary MGCT did not occur after radiotherapy. The prognosis was better than previous findings. Benign recurrence of GCTB could reflect the prognosis of MGCT.

Keywords: giant cell tumor of bone; malignancy in giant cell tumor; malignant transformation; prognosis; radiotherapy; recurrence; secondary malignancy.

Publication types

  • Review

MeSH terms

  • Adult
  • Bone Neoplasms*
  • Female
  • Giant Cell Tumor of Bone* / pathology
  • Giant Cell Tumor of Bone* / radiotherapy
  • Humans
  • Male
  • Neoplasm Recurrence, Local
  • Neoplasms, Second Primary*
  • Prognosis
  • Retrospective Studies
  • Sarcoma*

Grants and funding

This research received no external funding.