TURKISH JOURNAL OF ONCOLOGY 2025 , Vol 40 , Num 4
Gustave Roussy Immune Score in Operable Pancreatic Ductal Adenocarcinoma: Its Association with Quantitative 18F-FDG PET/CT Parameters and Histopathological Features, and Prognostic Significance
Kerim ŞEKER1,Süleyman KOÇ2,Hatice ÖZER3,Zekiye HASBEK1
1Department of Nuclear Medicine, Sivas Cumhuriyet University, Faculty of Medicine, Sivas-Türkiye
2Department of General Surgery, Sivas Cumhuriyet University Faculty of Medicine, Sivas-Türkiye
3Department of Medical Pathology, Sivas Cumhuriyet University Faculty of Medicine, Sivas-Türkiye
DOI : 10.5505/tjo.2025.4687 OBJECTIVE
This study aimed to investigate the relationship and prognostic value of the Gustave Roussy Immune Score (GRIm Score), quantitative 18F-FDG PET/CT parameters, and histopathological features in operable pancreatic ductal adenocarcinoma (PDAC) patients.

METHODS
We retrospectively analysed 18F-FDG PET/CT data, routine pre-operative blood tests (for GRIm Score), and post-surgical pathology (LVI, PNI, etc.) from 41 operable PDAC patients (2016-2024). The GRIm Score (0-3) was determined using LDH, Albumin, and NLR. Patients were categorized into low (0-1) and high (2-3) GRIm groups for statistical evaluation.

RESULTS
No significant correlation was found between the GRIm score and PET/CT or pathology features. Mean overall survival was 12.97 months. Patients with high GRIm scores showed significantly shorter survival (6.2 months vs. 16.7 months, p<0.001). Multivariate survival analysis confirmed that both the GRIm score (HR=10.258, p<0.001) and the presence of LVI (HR=14.899, p=0.019) were independent prognostic factors. Other parameters did not show a significant association with survival.

CONCLUSION
The GRIm score, easily and cost-effectively calculated from routine blood tests, holds significant and independent prognostic value in operable PDAC patients. Its independence from conventional tumor features suggests promising potential for assessing prognosis. Keywords : 18F-FDG PET/CT; GRIm score; histopathology; pancreatic ductal adenocarcinoma; survival