Soft-tissue sarcoma is a challenging disease area because it is a heterogeneous disease with over 50 different subtypes (1). Second, it is a rare disease that accounts for over 20% of all pediatric solid malignant cancers and less than 1% of all adult solid malignant cancers (2).

Tumor initiation, progression, and responses to therapy are highly related to the tumor microenvironment, including cells and molecules of the immune system (3,4).

The expression rate of PD-L1 in human malignant tumors has been reported to vary from 19 to 92% and is associated with the progression and poor prognosis of various human cancers. In addition, intratumor infiltration of PD1-positive T-cells was positively correlated with the progression of human malignant tumors (5).

PD-L1 expression is rarely studied in soft tissue sarcoma. In one study that analyzed PD-L1 expression in 82 STS patients, PD-L1 expression was identified in 43% of STS patients and considered an independent adverse prognostic factor for the overall survival of STS patients (6).

We evaluated the expression of PD-L1 in soft tissue sarcoma specimens on paraffin-embedded tissue by immunohistochemistry. Our primary endpoint was the detection of the prevalence of PD-L1 expression in soft tissue sarcoma and its correlation with the clinicopathological features of the tumor. The secondary endpoint was the prognostic significance of PD-L1 in soft tissue sarcoma.

This study comprised a total of 50 specimens of surgically removed, formalin-fixed, and paraffin-embedded tumors. Cases were retrieved from the archives of Ain Shams University Hospital during the period from 2011 to 2017 in Cairo, Egypt.

Cases with adequate paraffin tissue samples were included in this study. The study was carried out with full local ethics approval. Various types of soft tissue sarcomas were included. Tumors were classified according to WHO/2013 pathological classification (fourth edition) (8), including desmoid and GIST and excluding bone sarcomas.

We reviewed the medical records for patient data, including age, race, tumor location, histological type and grade, tumor stage based on the seventh edition of the American Joint Committee on Cancer guideline of tumor-node-metastasis (TNM) classification, and resection margin status for resected tumors.

The cohort consisted of 27 (54%) female and 23 (46%) male patients with a median age of 42.5 years (range 18–79). Most tumors were of grade G2 (34%) and G3 (46%). The majority of the patients did not have metastases at presentation (92%). The most frequent histologic subtypes were liposarcoma (22%), followed by leiomyosarcoma (18%) and ULP (15%). Eighty-four percent (42 patients) underwent surgical treatment, with R0 margins in 38% of these patients. Thirty percent of patients developed metastases, with the lung as the predominant site (see Table 2).

In this study, we evaluated the expression of PD-L1 in various sarcoma subtypes and explored its correlations with different clinicopathological features and survival. PD-L1 expression in tumor cells was observed in 12 (24%) of 50 soft tissue sarcoma cases of different subtypes. The tumor cell PD-L1 expression patterns vary in the literature (7), i.e., reports of positive expression in 12% of tumor cells vs. reports that described positive expression in 48% and 65% (11,14). Table 3 summarized the most relevant data published in this area.

This discrepancy of the published data may be related to the lack of harmonization of the PD-L1 assay as well as the use of different antibody types and different definitions of a positive result with a specific cut-off. The second reason is related to soft tissue sarcoma itself, as it is not one disease but a heterogeneous group of diseases. We report here a significant variation in PD-L1 expression based on the histological subtypes (p = 0.018). This finding was also reported by others, who found that the histological subtypes of soft tissue sarcoma were significantly correlated with PD-L1 expression (p = 0.004) (5).

Other than the histological subtypes, we did not identify relationships between tumor PD-L1 expression and clinicopathological characteristics. These results are similar to those of (7) and (5) and in contrast to those of (14), who reported that PD-L1 expression was also significantly associated with higher tumor stage, deep-seated sarcoma, distant metastasis, higher histologic grade, tumor differentiation, and tumor necrosis. Furthermore (21), found that PD-L1 expression was significantly associated with high tumor grade and the age of patients with soft tissue sarcomas.

In other solid malignancies, the level of PD-1/PD-L1 expression is considered an independent factor for worse survival. For example, in renal cell carcinoma, the expression of PD-1 in tumor-infiltrating lymphocytes is considered a poor prognostic factor for survival (21). Additionally, in gastric cancer and lung cancer, PD-L1 expression was established as an independent prognostic factor for poor OS (15,12).

We found that soft tissue sarcoma patients with positive PD-L1 expression showed a median OS of 11 months compared with 19 months for patients with negative PD-L1 expression and a mean PFS of 6 months compared with 11 months for patients with negative PD-L1 expression. We consider this finding clinically significant, as the p-value was 0.1 for OS and 0.2 for PFS and therefore indicated a trend. These results confirm the data of (7), who reported a median OS of 10.4 months in PD-L1-positive patients vs. not reached in PD-L1-negative patients, with a p-value of 0.8 owing to the small sample size, according to the author’s interpretation.

In contrast (5), found that the expression of PD-L1 in tumor tissue significantly predicted shortened OS [5 years OS rate, 48% vs. 68%; hazard ratio (HR) = 2.545; 95% confidence interval (CI) = 1.16–5.56; p = 0.015] (14). reported that soft tissue sarcoma patients with a PD-1+/PD-L1+ phenotype had the shortest survival time and a more progressive STS phenotype. Even in low-stage STS, the five-year survival rate of the PD-1+/PD-L1+ subgroup was only 29%, and the ten-year survival rate was 0%. In contrast, the ten-year survival rates of the PD-1−/PD-L1− subgroups were 94% in low-stage STS and 67% in high-stage STS.

The limitations of our analysis are the heterogeneity of the samples, the small sample size, and the imbalanced histological subtypes between the two groups. The study findings have to be confirmed on a larger scale, involving more patients as well as defined larger groups of each subtype.

Additionally, evaluating PD-L1 expression at an isolated time point or at the interval between biopsy and treatment may not represent its true prevalence. Furthermore, the primary disease and the presence of a metastatic site may further impact the value of PD-L1 expression, and the analysis in our study involved samples mainly originating from early nonmetastatic stages. However, it is well known that this may reflect failed immune surveillance and tumor escape in advanced and metastatic disease.