Abstract

Aim. To report our preliminary single-center experience with cytoreductive surgery (CRS) plus hyperthermic intraperitoneal chemotherapy (HIPEC) for management of peritoneal sarcomatosis (PS). Methods. Eleven patients were retrospectively analyzed for perioperative details. Results. Cytoreduction completeness (CC-0/1) was achieved in all patients with median peritoneal cancer index (PCI) of 14 ± 8.9 (range: 3–29). Combination cisplatin + doxorubicin HIPEC chemotherapy was used in 6 patients. Five patients received intraoperative radiation therapy (IORT). The median operative time, estimated blood loss, and hospital stay were 8 ± 1.4 hours (range: 6–10), 1000 ± 250 mL (range: 700–3850), and 11 ± 2.4 days (range: 7–15), respectively. Major postoperative Clavien-Dindo grade III/IV complications occurred in 1 patient and none developed HIPEC chemotherapy-related toxicities. The median overall survival (OS) and disease-free survival (DFS) after CRS + HIPEC were 28.3 ± 3.2 and 18.0 ± 4.0 months, respectively. The median follow-up time was 12 months (range: 6–33). Univariate analysis of several prognostic factors (age, gender, PS presentation/pathology, CC, PCI, HIPEC chemotherapy, and IORT) did not demonstrate statistically significant differences of OS and DFS. Conclusion. CRS + HIPEC appear to be feasible, safe, and offer survival oncological benefits. However, definitive conclusions cannot be deduced.

Highlights

  • Soft tissue sarcomas (STSs) are quite rare neoplasms accounting for roughly 1% of all adult solid malignancies [1]

  • The natural biological behavior of STSs is characterized by an increased tendency for disease dissemination [4] and recurrence [5, 6]

  • The aim of this study is to report our single-center experience regarding the use of cytoreductive surgery (CRS) plus hyperthermic intraperitoneal chemotherapy (HIPEC) for management of patients with primary and recurrent peritoneal sarcomatosis (PS)

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Summary

Introduction

Soft tissue sarcomas (STSs) are quite rare neoplasms accounting for roughly 1% of all adult solid malignancies [1]. The natural biological behavior of STSs is characterized by an increased tendency for disease dissemination [4] and recurrence [5, 6]. Modes of disease dissemination include local invasion, peritoneal infiltration, blood-borne, and rarely lymph-borne spread [4]. Around 35% to 82% of all STSs will experience disease recurrence after the initial surgical management [5, 6]. The vast majority of these recurred STSs (80– 90%) will progress and present as peritoneal sarcomatosis (PS)—multinodular intraperitoneal dissemination of STS [7]. This PS is especially true for abdominal/retroperitoneal STSs; trunk and limb STSs only exceptionally result in PS. It should be recognized that PS may be the primary presentation in a proportion of patients [8]

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