Post-radiation sarcomas. Clinical outcome of 52 Patients

J Surg Oncol. 2012 May;105(6):570-6. doi: 10.1002/jso.22122. Epub 2011 Oct 19.

Abstract

Background: Previous studies reported on post-radiation sarcomas. However, the incidence, latency from radiation therapy, treatment, and survival has been difficult to evaluate. We performed a retrospective, single-institutional study to determine these factors for post-radiation sarcomas.

Materials and methods: We retrospectively studied 52 patients with post-radiation sarcomas diagnosed and treated from 1985 to 2011. The mean age was 49 years; 45 patients had bone and 7 soft tissue sarcoma. The mean follow-up was 45 months. Survival was analyzed with respect to age at diagnosis, type (bone vs. soft tissue), histology, location (trunk vs. extremities), size, and surgical treatment (resection vs. amputation).

Results: The risk of post-radiation sarcoma was 0.06% at a mean latency of 15 years (3-50 years) after radiation therapy. The most common histology was osteosarcoma followed by malignant fibrous histiocytoma and fibrosarcoma; all sarcomas were high grade. Survival of the patients with post-radiation sarcomas was 85% at 1 year, 51% at 2 years, 48% at 3 years, and 45% at 5 years. Univariate predictor of survival was only the type of the sarcoma. No variable was significant in multivariate analysis.

Conclusions: Prognosis of post-radiation sarcomas is poor; the type of the sarcomas is the only significant variable for survival.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Bone Neoplasms / mortality*
  • Bone Neoplasms / pathology
  • Bone Neoplasms / therapy
  • Female
  • Follow-Up Studies
  • Humans
  • Male
  • Middle Aged
  • Neoplasm Metastasis
  • Neoplasms / radiotherapy
  • Neoplasms, Radiation-Induced / mortality*
  • Neoplasms, Radiation-Induced / pathology
  • Neoplasms, Radiation-Induced / therapy
  • Retrospective Studies
  • Sarcoma / mortality*
  • Sarcoma / pathology
  • Sarcoma / therapy
  • Soft Tissue Neoplasms / mortality*
  • Soft Tissue Neoplasms / pathology
  • Soft Tissue Neoplasms / therapy
  • Survival Rate
  • Young Adult