Cancer Testis Antigens and Immunotherapy: Expression of PRAME Is Associated with Prognosis in Soft Tissue Sarcoma

GND
14075461X
ORCID
0000-0002-5028-5062
Zugehörigkeit
Department of General, Visceral and Transplantation Surgery, University Hospital, Ludwig-Maximilians-Universität (LMU) Munich, Marchioninistr. 15, 81377 Munich, Germany, Markus.Albertsmeier@med.uni-muenchen.de
Albertsmeier, Markus;
GND
1263033237
Zugehörigkeit
Department of General, Visceral and Vascular Surgery, Friedrich-Schiller Universität Jena, Am Klinikum 1, 07743 Jena, Germany, annelore.altendorf-hofmann@gmx.de
Altendorf-Hofmann, Annelore;
GND
1174829524
ORCID
0000-0003-3708-8264
Zugehörigkeit
Department of Internal Medicine III, University Hospital, Ludwig-Maximilians-Universität (LMU) Munich, Marchioninistr. 15, 81377 Munich, Germany, Lars.Lindner@med.uni-muenchen.de
Lindner, Lars H.;
GND
111942012
ORCID
0000-0002-3494-6561
Zugehörigkeit
Department of Internal Medicine III, University Hospital, Ludwig-Maximilians-Universität (LMU) Munich, Marchioninistr. 15, 81377 Munich, Germany, rolf.issels@med.uni-muenchen.de
Issels, Rolf D.;
GND
139206752
Zugehörigkeit
Department of Internal Medicine III, University Hospital, Ludwig-Maximilians-Universität (LMU) Munich, Marchioninistr. 15, 81377 Munich, Germany, kampmann77@gmail.com
Kampmann, Eric;
ORCID
0000-0002-1347-1173
Zugehörigkeit
Musculoskeletal Oncology, Department of Orthopaedic Surgery, Physical Medicine and Rehabilitation, University Hospital, Ludwig-Maximilians-Universität (LMU) Munich, Marchioninistr. 15, 81377 Munich, Germany, hans_roland.duerr@med.uni-muenchen.de
Dürr, Hans-Roland;
Zugehörigkeit
Munich Cancer Registry (MCR) of the Munich Tumour Centre (TZM), Institute for Medical Information Processing, Biometry, and Epidemiology (IBE), University Hospital, Ludwig-Maximilians-Universität (LMU) Munich, Marchioninistr. 15, 81377 Munich, Germany, gabriele.schubert-fritschle@med.uni-muenchen.de
Schubert-Fritschle, Gabriele;
Zugehörigkeit
Department of General, Visceral and Transplantation Surgery, University Hospital, Ludwig-Maximilians-Universität (LMU) Munich, Marchioninistr. 15, 81377 Munich, Germany, martin.angele@med.uni-muenchen.de
Angele, Martin K.;
Zugehörigkeit
Institute of Pathology, Ludwig-Maximilians-Universität (LMU) Munich, Thalkirchner Str. 36, 80337 Munich, Germany, Thomas.Kirchner@med.uni-muenchen.de
Kirchner, Thomas;
Zugehörigkeit
Department of Pathology, Memorial Sloan Kettering Cancer Center (MSKCC), New York, NY 1275, USA, jungblua@mskcc.org
Jungbluth, Achim A.;
GND
124286518
Zugehörigkeit
Institute of Pathology, Ludwig-Maximilians-Universität (LMU) Munich, Thalkirchner Str. 36, 80337 Munich, Germany, Thomas.Knoesel@med.uni-muenchen.de
Knösel, Thomas

: (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.

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