Cancer Res Treat.  2022 Apr;54(2):579-589. 10.4143/crt.2021.496.

Clinicopathologic Characteristics and Clinical Outcome of Localized Liposarcoma: A Single-Center Experience over 25 Years and Evaluation of PD-L1 Expression

Affiliations
  • 1Department of Oncology, Asan Medical Center University of Ulsan College of Medicine, Seoul, Korea
  • 2Center for Breast Cancer, National Cancer Center Korea, Goyang, Korea
  • 3Department of Orthopedic Surgery, Asan Medical Center University of Ulsan College of Medicine, Seoul, Korea
  • 4Department of Radiation Oncology, Asan Medical Center University of Ulsan College of Medicine, Seoul, Korea
  • 5Department of Radiology, Asan Medical Center University of Ulsan College of Medicine, Seoul, Korea
  • 6Department of Pathology, Asan Medical Center University of Ulsan College of Medicine, Seoul, Korea

Abstract

Purpose
For liposarcoma (LPS), clinical course and proper treatment strategies have not been well-established. Recently, immune-checkpoint inhibitors have shown potential efficacy in LPS. We aimed to describe the clinical course of LPS and evaluate the clinical impact of programmed death-ligand 1 (PD-L1).
Materials and Methods
We reviewed all consecutive patients (n=332) who underwent curative-intent surgery for localized LPS at Asan Medical Center between 1989 and 2017. PD-L1 testing was performed in well-differentiated and dedifferentiated LPS.
Results
The median age was 56 years with males comprising 60.8%. Abdomen-pelvis (47.6%) and well-differentiated (37.7%) were the most frequent primary site and histologic subtype, respectively. During a median follow-up of 81.2 months, recurrence was observed in 135 (40.7%), and 86.7% (117/135) were loco-regional. Well-differentiated subtype (hazard ratio [HR], 0.38), abdomen-pelvis origin (HR, 2.43), tumor size larger than 5 cm (HR, 1.83), positive resection margin (HR, 2.58), and postoperative radiotherapy (HR, 0.36) were significantly related with recurrence-free survival as well as visceral involvement (HR, 1.84) and multifocality (HR, 3.79) in abdomen-pelvis LPS. PD-L1 was positive in 31.5% (23/73) and 51.3% (39/76) of well-differentiated and dedifferentiated LPS, respectively, but had no impact on survival outcomes.
Conclusion
Clinical course of LPS was heterogeneous according to histology and anatomic location. Clear resection margin was important to lower recurrence and postoperative radiotherapy might have additional benefit. A decent portion of well-differentiated and dedifferentiated LPS were positive for PD-L1, but its prognostic role was unclear. Further research is needed to determine clinical implications of PD-L1, especially for advanced-stage LPS with unmet needs for effective systemic treatment.

Keyword

Sarcoma; Liposarcoma; Retrospective analysis; Prognosis; Immunotherapy; Programmed death-ligand 1

Figure

  • Fig. 1 Survival outcomes of localized liposarcoma (LPS) after surgery according to cancer characteristics. Recurrence-free survival and overall survival curve of patients with localized LPS according to age (A, B), histologic subtype (C, D), primary tumor site (E, F), and primary tumor size (G, H), the estimated median survival time (95% confidence interval) is presented underneath the graphs.

  • Fig. 2 Survival outcomes of localized liposarcoma (LPS) after surgery according to applied treatment. Recurrence-free survival and overall survival curve of patients with localized LPS according to resection margin (A, B), postoperative radiotherapy (C, D), and postoperative chemotherapy (E, F), the estimated median survival time (95% confidence interval) is presented underneath the graphs.

  • Fig. 3 Representative images of programmed death-ligand 1 (PD-L1) expression and survival outcomes according to PD-L1 status. (A) Dedifferentiated liposarcoma (LPS) shows immunopositivity for PD-L1 (SP263) with diffuse and homogenous pattern (×200). Placenta tissue is used as positive control (inset). (B) Well-differentiated LPS shows patchy immunoreactivity for PD-L1 (SP263) (×200). (C) Tumor cells of dedifferentiated LPS are negative for PD-L1 (SP263) (×100). There was no difference in recurrence-free survival (D) and overall survival curve (E) according to PD-L1 status. The estimated median survival time (95% confidence interval) is presented underneath the graphs.


Reference

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