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Published on: August 14, 2021
Surgical resection for recurrent retroperitoneal leiomyosarcoma and liposarcoma
Michael J Nathenson1, Constance M Barysauskas2, Robert A Nathenson3
1Center for Sarcoma and Bone Oncology, Dana-Farber Cancer Institute, 450 Brookline Ave, Boston, MA, 02215, USA. michaelj_nathenson@dfci.harvard.edu.
Retroperitoneal sarcomas, including liposarcoma and leiomyosarcoma, show varying survival rates and prognostic factors. This study highlights differences in incidence among racial groups and confirms key predictors of patient outcomes.
Area of Science:
- Oncology
- Surgical Oncology
- Cancer Research
Background:
- Retroperitoneal soft tissue sarcomas (STS) are rare, with high recurrence rates.
- The University of Maryland Medical Center (UMMC) serves a diverse patient population for STS treatment.
Purpose of the Study:
- To review UMMC's treatment experience with retroperitoneal STS.
- To analyze outcomes for liposarcoma (LPS) and leiomyosarcoma (LMS) patients.
Main Methods:
- Retrospective review of 49 patients with LPS or LMS treated 2000-2013.
- Kaplan-Meier plots and log-rank tests used for survival analysis (PFS, OS).
Main Results:
- Median overall survival (OS) was 6.3 years; 2-year OS rate was 81%.
- Median progression-free survival (PFS) was 1.8 years; 2-year PFS rate was 45%.
- Leiomyosarcoma showed higher incidence in African Americans; liposarcoma in Caucasians. OS and PFS influenced by AJCC stage, grade, tumor size, and resection extent.
Conclusions:
- Leiomyosarcoma may be more common in African Americans.
- Grade, tumor size, AJCC stage, histology, and resection extent are critical prognostic factors for retroperitoneal STS.
- Further research into biological features of LPS and LMS is warranted.
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