Development and validation of the gastric risk immuno-progression score (GRIPS) in advanced gastric and gastroesophageal junction adenocarcinoma treated with first-line chemotherapy plus nivolumab: Results from the ORACLE study.
Abstract
4062 Background: The addition of nivolumab to chemotherapy is approved for advanced gastric and gastroesophageal junction (GEJ) adenocarcinoma with PD-L1 CPS ≥5. Identifying predictive tools for disease progression in this setting remains a clinical need. This study introduces the Gastric Risk Immuno-Progression Score (GRIPS), a novel score derived from variables associated with progression-free survival (PFS) in a real-world cohort. Methods: We conducted a multicenter retrospective study on 90 patients with gastric/GEJ adenocarcinoma treated with first-line chemotherapy plus nivolumab between 2022 and 2024. The GRIPScore was constructed using five dichotomous variables associated with unfavorable PFS in univariate analysis: Neutrophil-to-Lymphocyte Ratio (NLR > 2.68), ECOG Performance Status (≥2), Smoking status (never smoker), CA19.9 at diagnosis (UNL) and primary tumor resection (no resection). Each variable was scored as 1 (prognostically negative) or 0 (prognostically positive), and a total score (0–5) was calculated. Patients were categorized into low-risk (GRIPS 0–2) and high-risk (GRIPS 3–5) groups. PFS and OS were analyzed using Kaplan-Meier methods. Hazard Ratios (HRs) were calculated, and the discriminatory ability of the GRIPS was evaluated using Harrell's C-index. Results: The median PFS for the entire cohort was 11.55 months (95% CI: 7.60–13.26). Stratifying patients by GRIPS revealed a marked difference in outcomes between the low-risk and high-risk groups. Low-risk patients (GRIPS 0–2) had a median PFS of 13.16 months (95% CI: 9.01–18.91), while high-risk patients (GRIPS 3–5) had 4.11 months (95% CI: 2.37–11.77). This difference was significant (log-rank test, p = 0.0023; HR: 3.55, 95% CI: 1.58–8.02). Similarly, low-risk patients had a median OS of 21.25 months (95% CI: 13.77–21.25) compared to 11.90 months (95% CI: 4.03–16.10) for high-risk patients (log-rank test, p = 0.0313; HR: 2.73, 95% CI: 1.09–6.81). Harrell’s C-index for PFS was 0.648 (95% CI: 0.552–0.743), indicating moderate discriminatory ability. Conclusions: The GRIPS effectively stratifies patients with advanced gastric and gastroesophageal junction adenocarcinoma treated with a combination of chemotherapy + nivolumab into distinct risk groups for PFS and OS. High-risk patients experience significantly shorter survival, highlighting the potential clinical utility of GRIPS for personalized treatment strategies. Further prospective validation is warranted to refine its application in clinical practice. GRIPScore N° of patients (%) mOS (m) mPFS (m) Low-risk (0-2) 51 (45.9) 21.25 (95% CI: 13.77–21.25) 13.16 (95% CI: 9.01–18.91) High-risk (3-5) 21 (18.9) 11.90 (95% CI: 4.03–16.10) 4.11 (95% CI: 2.37–11.77) Not evaluable 18 (16.2)
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (20)
Dario Spanu
Medical Oncology Unit, University Hospital and University of Cagliari, Cagliari, Italy
Pina Ziranu
Medical Oncology Unit, University Hospital and University of Cagliari, Cagliari, Italy
Andrea Pretta
Medical Oncology Unit, University Hospital and University of Cagliari, Cagliari, Italy
Riccardo Cerantola
Department of Surgery, Oncology and Gastroenterology, University of Padua and Oncology Unit 3, Veneto Institute of Oncology IOV-IRCCS, Padua, Italy
Francesca Salani
Department of Translational Medicine Research and New Technologies in Medicine and Surgery, University of Pisa, Pisa, Italy
Silvia Ortolani
Ospedale San Bortolo AULSS 8 Berica, Vicenza, Italy
Emanuela Di Giacomo
Operative Research Unit of Medical Oncology, Fondazione Policlinico Universitario Campus Bio-Medico, Rome, Italy
Alessandra Pia D'Agata
Medical Oncology Unit, University Hospital and University of Cagliari, Cagliari, Italy
Giada Grelli
Azienda Ospedaliero-Universitaria Pisana, Pisa, Italy
Adelaide Mazzocca
Clinical Oncology, Department of Clinical and Molecular Sciences, University Politecnica delle Marche - University Hospital "Azienda Ospedaliero Universitaria delle Marche", Ancona, Italy
Eleonora Perissinotto
Department of Surgery, Oncology and Gastroenterology, University of Padua, and Medical Oncology 1, Veneto Institute of Oncology (IOV-IRCCS), Padua, Italy
Laura Pala
Humanitas University, Milan, Italy
Francesco Mangogna
Azienda Ospedaliero-Universitaria Pisana, Pisa, Italy
Jessica Lucchetti
Operative Research Unit of Medical Oncology, Fondazione Policlinico Universitario Campus Bio-Medico, Rome, Italy
Riccardo Giampieri
Lorenzo Fornaro
Azienda Ospedaliero–Universitaria Pisana, Pisa, Italy
Alessandro Pastorino
Giuseppe Aprile
Floriana Nappo
Medical Oncology 1, Veneto Institute of Oncology IOV–IRCCS, Padua, Italy
Mario Scartozzi
Medical Oncology Unit, University Hospital and University of Cagliari, Cagliari, Italy