Publication

Predictors of Disease-Free and Overall Survival in Retroperitoneal Sarcomas: A modern 16 year Multi-Institutional Study from the United States Sarcoma Collaboration (USSC)

Downloadable Content

Persistent URL
Last modified
  • 05/21/2025
Type of Material
Authors
    Patrick B. Schwartz, University of WisconsinKara Vande Walle, University of WisconsinEmily R. Winslow, University of WisconsinCecilia G. Ethun, Emory UniversityThuy B. Tran, Stanford UniversityGeorge Poultsides, Stanford UniversityJennifer Tseng, University of ChicagoKevin Roggin, University of ChicagoValerie Grignol, Ohio State UniversityJohn Harrison Howard, Ohio State UniversityBradley A. Krasnick, Washington UniversityRyan C. Fields, Washington UniversityHarveshp Mogal, Medical College of WisconsinCallisia N. Clarke, Medical College of WisconsinRebecca Senehi, Wake Forest UniversityKonstantinos Votanopoulos, Wake Forest UniversityKenneth Cardona, Emory UniversityDaniel E. Abbott, University of Wisconsin
Language
  • English
Date
  • 2018-02-01
Publisher
  • Hindawi
Publication Version
Copyright Statement
  • © 2019 Patrick B. Schwartz et al.
License
Final Published Version (URL)
Title of Journal or Parent Work
ISSN
  • 1357-714X
Volume
  • 25
Start Page
  • S195
End Page
  • S195
Grant/Funding Information
  • This research was not funded by any specific grant, but was supported by Daniel Abbott, MD, as a part of his employment.
Abstract
  • Background. Retroperitoneal sarcomas (RPS) comprise approximately 15% of all soft-tissue sarcomas and frequently associated with significant morbidity and as little as 30% 5-year survival. Here, we provide a large, contemporary, and multi-institutional experience to determine which tumor, patient, and treatment characteristics are associated with long-term outcomes in RPS. Methods. 571 patients with primary RPS were identified from the United States Sarcoma Collaboration (USSC). RPS patients who underwent resection from January 2000 to April 2016 were included with patient, tumor, and treatment-specific variables investigated as independent predictors of survival. Survival analyses for disease-free and overall survival were conducted using Kaplan-Meier and Cox proportional hazards model methods. Results. The study cohort was 55% female, with a median age of 58.9 years (IQR: 48.6-70.0). The most common tumor histiotypes were liposarcoma (34%) and leiomyosarcoma (28%). Median follow-up was 30.6 months (IQR: 11.2-60.4). Median disease-free survival was 35.3 months (95% CI: 27.6-43.0), with multivariate predictors of poorer disease-free survival including higher grade tumors, nodal-positive disease, and multivisceral resection. Median overall survival was 81.6 months (95% CI: 66.3-96.8). Multivariate predictors of shorter overall survival included higher grade tumors, nodal-positive and multifocal disease, systemic chemotherapy, and grossly positive margins (R2) following resection. Conclusions. The strongest predictors of disease-free and overall survival are tumor-specific characteristics, while surgical factors are less impactful. Nonsurgical therapies are not associated with improved outcomes despite persistent interest and utilization. Complete macroscopic resection (R0/R1) remains a persistent potentially modifiable risk factor associated with improved overall survival in patients with retroperitoneal sarcomas.
Author Notes
Keywords
Research Categories
  • Health Sciences, Oncology
  • Health Sciences, Medicine and Surgery

Tools

Relations

In Collection:

Items