1. Survival Outcome and Prognostic Factors After Pulmonary Metastasectomy in Sarcoma Patients: A 18-Year Experience at a Single High-volume Referral Center.
- Author
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Cariboni U, De Sanctis R, Giaretta M, Voulaz E, Morenghi E, Colombo P, Novellis P, Bottoni E, Errico V, Crepaldi A, Marrari A, Navarria P, Ascolese AM, Testori A, Scorsetti M, Quagliuolo V, Santoro A, and Alloisio M
- Subjects
- Adolescent, Adult, Aged, Aged, 80 and over, Bone Neoplasms mortality, Disease-Free Survival, Female, Humans, Lung Neoplasms mortality, Male, Metastasectomy, Middle Aged, Prognosis, Retrospective Studies, Sarcoma mortality, Soft Tissue Neoplasms mortality, Treatment Outcome, Bone Neoplasms pathology, Lung Neoplasms secondary, Lung Neoplasms surgery, Sarcoma pathology, Soft Tissue Neoplasms pathology
- Abstract
Background: Metastatic sarcoma patients have a poor prognosis with 3-year survival rate of 25%. About 30% of them present isolated lung metastases. We aimed to analyze the clinical outcome of sarcoma patients undergoing pulmonary metastasectomy (PM) and prognostic factors associated with local control, disease-free, and overall survival (OS)., Patients and Methods: All sarcoma patients undergoing PM at Humanitas Cancer Center were retrospectively reviewed. Analyzed variables included clinicopathologic, surgical, and survival data. Exclusion criterion comprised a follow-up period inferior to 1 year. A univariable and multivariable Cox regression analysis was performed (P<0.05)., Results: In total, 154 patients underwent PM from 1997 to 2015. Total complication rate was 7.1%. The median follow-up was 24 months. The median OS was 35.4 months from initial metastasectomy. In univariable analysis, we identified as significant negative prognostic factors a disease-free interval of <18 months, male sex, grading G3, and bilateral metastases. Three histology risk groups were defined according to OS: high risk (myxofibrosarcoma, malignant peripheral nerve sheath tumor, and Ewing sarcoma), intermediate risk (leiomyosarcoma, liposarcoma, and undifferentiated pleomorphic sarcoma), and low risk (synovial and chondrosarcoma) with a 3-year OS of 21.4%, 45.7%, and 74.1%, respectively. In multivariable analysis, male sex (P=0.042), bilateral metastases (P=0.004), and histology (intermediate vs. low-risk group, P=0.021; high vs. low-risk group, P<0.001) were identified as independent predictors of survival., Conclusions: PM for sarcoma is a valid therapeutic option. High-risk histologies and bilaterality of lung metastases are independent negative prognostic factors. A prognostic score to improve patient selection is proposed.
- Published
- 2019
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