Abstract

(1) Background: PRAME, NY-ESO-1, and SSX2 are cancer testis antigens (CTAs), which are expressed in testicular germ cells with re-expression in numerous cancer types. Their ability to elicit humoral and cellular immune responses have rendered them promising targets for cancer immunotherapy, but they have never been studied in a large and well-characterised cohort of soft tissue sarcomas (STS). (2) Methods: On a protein level, we examined PRAME, NY-ESO-1, and SSX2 expression in tumour tissues of 249 high-risk STS using immunohistochemistry. We correlated expression levels with clinicopathological parameters including tumour-infiltrating lymphocyte (TIL) counts, grading, and long-term survival. (3) Results: Expression of PRAME, NY-ESO-1, and SSX2 was observed in 25 (10%), 19 (8%), and 11 (4%) of 249 specimens with distinct patterns for histo-subtypes. Expression of PRAME was associated with shorter patient survival (p = 0.005) and higher grade (G2 vs. G3, p = 0.001), while NY-ESO-1 expression was correlated with more favourable survival (p = 0.037) and lower grade (G2 vs. G3, p = 0.029). Both PRAME and NY-ESO-1 expression were more frequent in STS with low TIL counts. In multivariate analysis, high PRAME and low SSX2 expression levels as well as metastatic disease and non-radical resections were independent predictors of shorter overall survival. (4) Conclusions: CTAs PRAME, NY-ESO-1, and SSX2 show distinct expression patterns in different STS subtypes. These results demonstrate their prognostic relevance and may guide future immunotherapeutic approaches in STS.

Highlights

  • Soft tissue sarcomas (STS) are a heterogenous group of rare malignant tumours originating from soft tissues that can occur in different parts of the human body

  • We analysed the expression of cancer-testis antigens (CTAs) PRAME, NY-ESO-1, and SSX2 as well as the presence of tumour-infiltrating lymphocytes (TILs) in a well-characterised cohort of high-grade soft tissue sarcoma patients

  • We found the expression of PRAME and the presence of a high number of TILs to be associated with shorter survival, while NY-ESO-1 expression was more frequent in patients with a more favourable prognosis

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Summary

Introduction

Soft tissue sarcomas (STS) are a heterogenous group of rare malignant tumours originating from soft tissues that can occur in different parts of the human body. Immunotherapy, which has been successfully introduced for several cancers, might be an option to individualise therapy of sarcoma patients [3]. Expression of cancer-testis antigens (CTAs) is restricted to germ cells and trophoblasts. They are aberrantly expressed in various types of cancer. Following their identification in malignant melanoma, CTAs have been detected in carcinomas of various sites, such as lung, ovary, urinary bladder, liver, and other organs [4]. CTAs can be highly immunogenic and are considered potential targets for immunotherapy of cancer [17]

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