Clinical importance of late recurrence in soft-tissue sarcomas
β Scribed by Gibbs, John F.; Lee, R. Jeffrey; Driscoll, Deborah L.; McGrath, Brian E.; Mindell, Eugene R.; Kraybill, William G.
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 118 KB
- Volume
- 73
- Category
- Article
- ISSN
- 0022-4790
No coin nor oath required. For personal study only.
β¦ Synopsis
Background and Objectives: Soft-tissue sarcomas (STS) represent a diverse histologic group of malignancies at risk for local and distant failure. We studied the impact of late (5 or more years) vs. early recurrence (less than 5 years) on subsequent outcome. Methods: Four hundred sixty-eight patients with STS treated between 1962 and 1992 were evaluated for late (n β«Χ‘β¬ 39; 8%) or early (n β«Χ‘β¬ 253; 54%) recurrence. Clinical and pathologic factors were reviewed. Survival data were analyzed by the Kaplan-Meier method and the log-rank test. Results: Of the 39 patients with a late recurrence (median follow-up 156 months), 18 patients had local recurrence, 7 patients developed distant recurrence, and 14 patients had local and distant recurrence. Thirty patients with late local and/or distant recurrence underwent complete or wide excision (n β«Χ‘β¬ 16), amputation (n β«Χ‘β¬ 4), or local resection (n β«Χ‘β¬ 10). The overall 5-year survival rate following late recurrence was 61%. The 5-year overall survival rate was statistically better for patients with a late local recurrence alone than for patients with distant failure, 94% vs. 36%, respectively (P β«Χ‘β¬ 0.003). Neither the site of the primary STS, age, primary margin status, nor histology had any effect on subsequent local or distant failure and subsequent survival. Conclusions: These data suggest that an aggressive approach is appropriate in patients who present with late recurrence (more than 5 years) following treatment of the primary STS. Impressive survival rates can be achieved in the treatment of local recurrences.
π SIMILAR VOLUMES
The clinical course of 117 patients who were treated for Stages IIB-IIIC sarcoma of soft tissues by the combined approach of radiation and surgery at MGH during the period 1971-1984 have been analyzed for an effect of adjuvant chemotherapy to improve clinical results. Thirty-two patients received ad
OFT TISSUE SARCOMAS are relatively uncom-S mon. The management of this group of sarcomas has been primarily surgical.1-\* Although radiation therapy has been used preoperatively, postoperatively, and for the treatment of recurrent, residual, or metastatic disease, its efficacy has not been fully ass