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Abstract
Purpose
Until now, results evaluating the expression of PSMA in ovarian cancer were sparse and contradictory. The aim was to reinvestigate the feasibility of a PSMA targeted theranostic approach in epithelial ovarian cancers with data from the tumour bank of a referring cancer centre.
Materials and methods
The OvaRessources Biological Resources Center database was screened from January 2004 to December 2017 to seek patients referred for the initial management of a serous epithelial ovarian cancer and for whom peritoneal histological samples were available in the tumour bank. Immunodetection of PSMA was performed to assess its cellular and neovascular expression. Slides were controlled by a certified pathologist, recorded as tiled tiff images and processed to compute the proportion of DAB stained surface.
Results
Of the 51 patients identified by the database screening, 32 patients were included resulting in 57 samples (32 pre-chemotherapy and 25 post-chemotherapy histological samples). Nine patients were chemo-sensitive, 10 were partially chemo-sensitive and 13 were chemo-resistant/refractory. In the entire dataset, the expression of PSMA was quasi-inexistent: %DABPSMA = 0.04 (± 0.12) %. There was no significant difference in the %DABPSMA of sensitive, partially sensitive and resistant/refractory patients. There was also no significant difference in %DABPSMA in tumours before and after chemotherapy in the 25 patients for whom both samples were available.
Conclusion
The present work demonstrates that PSMA expression is negligible and a fortiori non-sufficient to ensure its usefulness as a prognosticator or a target for a theranostic strategy in ovarian cancers.
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1 University Hospital, Nuclear Medicine Department, Caen, France (GRID:grid.411149.8) (ISNI:0000 0004 0472 0160); Normandy University, UNICAEN, INSERM 1086 ANTICIPE, Caen, France (GRID:grid.460771.3) (ISNI:0000 0004 1785 9671)
2 Normandy University, UNICAEN, INSERM 1086 ANTICIPE, Caen, France (GRID:grid.460771.3) (ISNI:0000 0004 1785 9671); UNICANCER, Comprehensive Cancer Centre F. Baclesse, Biological Ressources Centre OvaRESSOURCES, Caen, France (GRID:grid.418189.d) (ISNI:0000 0001 2175 1768)
3 Normandy University, UNICAEN, SF 4206 ICORE, CMABIO3, Caen, France (GRID:grid.460771.3) (ISNI:0000 0004 1785 9671)
4 Normandy University, UNICAEN, INSERM 1086 ANTICIPE, Caen, France (GRID:grid.460771.3) (ISNI:0000 0004 1785 9671)
5 Normandy University, UNICAEN, INSERM 1086 ANTICIPE, Caen, France (GRID:grid.460771.3) (ISNI:0000 0004 1785 9671); UNICANCER, Comprehensive Cancer Centre F. Baclesse, Biological Ressources Centre OvaRESSOURCES, Caen, France (GRID:grid.418189.d) (ISNI:0000 0001 2175 1768); UNICANCER, Department of Bio-Pathology, Comprehensive Cancer Centre F. Baclesse, Caen, France (GRID:grid.418189.d) (ISNI:0000 0001 2175 1768)
6 Normandy University, UNICAEN, INSERM 1086 ANTICIPE, Caen, France (GRID:grid.460771.3) (ISNI:0000 0004 1785 9671); UNICANCER, Department of Uro-Gynecological Oncology, Comprehensive Cancer Centre F. Baclesse, Caen, France (GRID:grid.418189.d) (ISNI:0000 0001 2175 1768)
7 Normandy University, UNICAEN, INSERM 1086 ANTICIPE, Caen, France (GRID:grid.460771.3) (ISNI:0000 0004 1785 9671); UNICANCER, Nuclear Medicine Department, Comprehensive Cancer Centre F. Baclesse, Caen, France (GRID:grid.418189.d) (ISNI:0000 0001 2175 1768)