Evidence map›Paper›PMID 41179670›Full record

ArticleFrontiers in oncology2025

Gustave Roussy immune score as an independent prognostic factor for treatment response and survival in advanced renal cell carcinoma treated with nivolumab in second-line and beyond.

Bülent Erdoğan, İvo Gökmen, Cagnur Elpen Kodaz, Ahmet Küçükarda, Didem Divriklioğlu, İsmail Bayrakçı, İlhan Hacıbekiroğlu, Esra Özen Engin, Muhammet Bekir Hacıoğlu, Erkan Özcan and 2 more

Abstract read
In one paragraph

Article in Frontiers in oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 2 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Bülent ErdoğanMedical Oncology, Trakya Universitesi Tip Fakultesi, Edirne, Türkiye.
İvo GökmenMedical Oncology, Trakya Universitesi Tip Fakultesi, Edirne, Türkiye.
Cagnur Elpen KodazFamily Medicine, Bilecik Seyh Edebali Universitesi, Bilecik, Türkiye.
Ahmet KüçükardaMedical Oncology, Trakya Universitesi Tip Fakultesi, Edirne, Türkiye.
Didem DivriklioğluMedical Oncology, Trakya Universitesi Tip Fakultesi, Edirne, Türkiye.
İsmail BayrakçıMedical Oncology, Trakya Universitesi Tip Fakultesi, Edirne, Türkiye.
İlhan HacıbekiroğluMedical Oncology, Sakarya Universitesi Tip Fakultesi, Sakarya, Türkiye.
Esra Özen EnginMedical Oncology, Sakarya Universitesi Tip Fakultesi, Sakarya, Türkiye.
Muhammet Bekir HacıoğluMedical Oncology, Trakya Universitesi Tip Fakultesi, Edirne, Türkiye.
Erkan ÖzcanMedical Oncology, Trakya Universitesi Tip Fakultesi, Edirne, Türkiye.
Gökhan ÖztürkMedical Oncology, Trakya Universitesi Tip Fakultesi, Edirne, Türkiye.
Hilmi KodazDepartment of Medical Oncology, Acıbadem Eskişehir Hospital, Eskişehir, Türkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Metastatic renal cell carcinoma (mRCC) represents a significant challenge due to variable patient outcomes despite advancements in treatment. Nivolumab, a programmed death-1 (PD-1) inhibitor, has demonstrated efficacy as a second-line or later therapy following progression on tyrosine kinase inhibitors (TKIs). However, identifying reliable prognostic biomarkers remains critical. The Gustave Roussy Immune (GRIm) score, incorporating serum albumin, lactate dehydrogenase (LDH), and neutrophil-to-lymphocyte ratio (NLR), may provide prognostic value in this context. Methods: This multicenter retrospective cohort study included 81 mRCC patients treated with nivolumab as second-line or subsequent therapy following progression on first-line TKIs (e.g., sunitinib or pazopanib). Patients were categorized into low (0-1) and high (2-3) GRIm score groups based on pre-treatment laboratory values. Outcomes included progression-free survival (PFS), overall survival (OS), and treatment response, assessed using RECIST criteria. Survival analyses were performed using Kaplan-Meier curves, and prognostic factors were identified through univariate and multivariate analyses. Results: The median age was 63 years, and 72.8% were male. Patients with low GRIm scores demonstrated significantly higher objective response rates (44.4% Conclusion: The GRIm score effectively stratifies mRCC patients treated with nivolumab, identifying those with significantly better survival and treatment responses. As a simple, cost-effective tool, it offers potential for integration into clinical practice to guide personalized treatment strategies. Further prospective studies are warranted to validate these findings.

Indexed as

GRIm scoremetastatic renal cell carcinomanivolumabprognostic biomarkersecond-line therapy

Identifiers

PMID41179670
PMCPMC12571565

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