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Association between GRIm score and response to nivolumab monotherapy in patients with advanced malignant melanoma
Sila Oksuz1, Oguzcan Kinikoglu2, Ugur Ozkerim2
1Department of Medical Oncology, Health Science University, Kartal Dr. Lütfi Kirdar City Hospital, 34865, Istanbul, Turkey. sila.oksuz@gmail.com.
Background/Objectives:
Malignant melanoma is an aggressive skin cancer with significant metastatic potential. Immune checkpoint inhibitors (ICIs), particularly those targeting the PD-1 pathway, have revolutionized treatment, improving survival rates. A PD-1 inhibitor, Nivolumab, has demonstrated durable responses in advanced melanoma patients. However, response variability necessitates predictive biomarkers for patient stratification.
Methods:
The Gustave Roussy Immune Score (GRIm Score) is a prognostic tool integrating lactate dehydrogenase (LDH), neutrophil-to-lymphocyte ratio (NLR), and albumin levels to predict ICI efficacy. This retrospective study evaluated the association between the GRIm Score and response to nivolumab monotherapy in 40 patients with stage IV malignant melanoma treated between 2020 and 2024. Patients were classified into low-risk (score 0-1) and high-risk (score 2-3) groups.
Results:
Results showed that patients with a low GRIm Score had significantly longer median progression-free survival (21.4 vs. 6.3 months, p = 0.003) and overall survival (26.5 vs. 7.2 months, p < 0.001). Multivariate analysis confirmed the GRIm Score as an independent prognostic factor (HR: 1.593, 95% CI: 1.156-2.197, p = 0.004), surpassing the predictive power of its components.
Conclusions:
This study is the first to validate the GRIm Score in malignant melanoma, suggesting it is a valuable biomarker for patient selection in immunotherapy trials. The findings highlight its potential in refining treatment decisions, though further validation in larger, multicenter cohorts is required.
Insights
The Gustave Roussy Immune Score (GRIm Score) predicts response to nivolumab immunotherapy in advanced melanoma. A low GRIm Score is linked to significantly longer progression-free and overall survival, aiding patient stratification.
Area of Science:
- Oncology
- Immunotherapy
- Biomarker Discovery
Background:
- Malignant melanoma is an aggressive skin cancer with high metastatic potential.
- Immune checkpoint inhibitors (ICIs), like nivolumab, have improved outcomes in advanced melanoma.
- Predictive biomarkers are crucial for stratifying patients and optimizing ICI therapy.
Purpose of the Study:
- To evaluate the Gustave Roussy Immune Score (GRIm Score) as a prognostic tool for predicting response to nivolumab monotherapy in stage IV malignant melanoma.
- To assess the association between the GRIm Score and clinical outcomes, including progression-free survival (PFS) and overall survival (OS).
Main Methods:
- Retrospective analysis of 40 stage IV malignant melanoma patients treated with nivolumab (2020-2024).
- Calculation of the GRIm Score based on lactate dehydrogenase (LDH), neutrophil-to-lymphocyte ratio (NLR), and albumin levels.
- Classification of patients into low-risk (score 0-1) and high-risk (score 2-3) groups.
Main Results:
- Patients with a low GRIm Score demonstrated significantly longer median PFS (21.4 vs. 6.3 months, p=0.003) and OS (26.5 vs. 7.2 months, p<0.001).
- Multivariate analysis identified the GRIm Score as an independent prognostic factor (HR: 1.593, p=0.004).
- The GRIm Score showed superior predictive power compared to its individual components.
Conclusions:
- This study provides the first validation of the GRIm Score in malignant melanoma patients treated with nivolumab.
- The GRIm Score is a valuable biomarker for patient selection in immunotherapy trials and refining treatment decisions.
- Further validation in larger, multicenter cohorts is warranted to confirm these findings.
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