World Journal of Surgery · 2010 · 48 citations · 20 references
MedicineOncologySurgerySurgical OncologySurvival AnalysisThoracic OncologyCancer Survival AnalysisChest Wall TumorsMalignant NeoplasmsSarcoma SurgerySoft Tissue SarcomasChest Wall RecurrenceChest Wall Sarcoma SurgeryChest Wall SarcomasChest Wall Tumor MarginsChest Wall Tumor ResectionChondrosarcoma RecurrenceLocal Tumor RecurrencePrognostic Factors Analysis
BACKGROUND: Wide resection with tumor-free margins is necessary in soft-tissue sarcomas to minimize local recurrence and to contribute to long-term survival. Information about treatment outcome and prognostic factors of adult sarcoma requiring chest wall resection (CWR) is limited. METHODS: Sixty consecutive patients were retrospectively studied for overall survival (OS), local recurrence-free survival (LRFS), and disease-free survival (DFS). Twenty-one prognostic factors regarding survival were analyzed by univariate analysis using the Kaplan-Meier method and the log-rank test. RESULTS: With a median survival of 2.5 years, the OS was 46% (33%) at 5 (10) years. The LRFS was 64% at 5 and 10 years, and the DFS was 30% and 25% at 5 and 10 years. At the end of the study period, 26 patients (43%) were alive, of which 20 patients (33%) had no evidence of disease and 40 patients (67%) had no chest wall recurrence. In the group of 9 patients with a radiation-induced soft-tissue sarcoma, the median survival was 8 months. Favorable outcome in univariate analysis in OS and LRFS applied for the low-grade sarcoma, bone invasion, and sternal resection. For OS only, age below 60 years and no radiotherapy were significant factors contributing to an improved survival. CWR was considered radical (R0) at the pathological examination in 43 patients. There were 52 patients with an uneventful recovery. There was one postoperative death. CONCLUSIONS: CWR for soft-tissue sarcoma is a safe surgical procedure with low morbidity and a mortality rate of less than 1%. With proper patient selection acceptable survival can be reached in a large group of patients. Care must be given to patients with radiation-induced soft-tissue sarcoma who have a significantly worse prognosis.
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Soft tissue sarcomas of adults: state of the translational science.
Ernest C. Borden, Laurence H. Baker, Robert S. Bell et al. · PubMed · 2003 · 616 citations
Radiation‐induced sarcomas after radiotherapy for breast carcinoma
Youlia Kirova, Jacques R. Vilcoq, Bernard Asselain et al. · Cancer · 2005 · 249 citations · Full text