Resection of Recurrent Pelvic Soft Tissue Sarcoma: Is the Risk Worth the Reward?

Eyal Mor*, Dan Assaf, Shanie Shemla, Eytan Ben-Ami, Danielle Mor-Hadar, Mirit Halfon, Shachar Laks, David Hazzan, Daria Perelson, Douglas Zippel, Almog Ben-Yaacov, Aviram Nissan, Mohammad Adileh

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Introduction: Soft tissue sarcomas (STS) of the pelvis present a surgical and oncological challenge. We investigated the outcomes of patients undergoing resection of pelvic sarcomas. Methods: A retrospective analysis of all patients who underwent surgical resection for STS between 2014 and 2021 at a tertiary academic referral center (n = 172). Included all patients with primary or recurrent STS which originated or extended to the pelvic cavity (n = 29). Results: The cohort was divided into primary pelvic sarcomas (n = 18) and recurrent pelvic sarcomas (rPS, n = 11). Complete R0/R1 resection was achieved in 26 patients (89.6%). The postoperative complication rate was 48.3%. The rate of major complications was 27.5%. The median time of follow-up from surgery was 12.3 months (range, 0.6-60.3 months). Disease-free survival was superior in the primary pelvic sarcomas group compared to the rPS group (P = 0.002). However, there was no significant difference in overall survival, (P = 0.52). Univariant and multivariant analyses identified rPS group (Hazard Ratio 8.68, P = 0.006) and resection margins (Hazard Ratio 6.29, P = 0.004) to be independently associated with disease-free survival. Conclusions: We have demonstrated that achieving R0/R1 resection is feasible. Oncological outcomes are favorable for primary tumors, whereas recurrent tumors exhibit early recurrences. Consideration of resection of recurrent pelvic STS should involve a careful multidisciplinary evaluation.

Original languageEnglish
Pages (from-to)914-922
Number of pages9
JournalJournal of Surgical Research
Volume283
DOIs
StatePublished - Mar 2023

Keywords

  • Pelvic sarcoma
  • Recurrent sarcoma
  • Retroperitoneal sarcoma

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