Evidence map›Paper›PMID 41813880›Full record

ArticleScientific reports2026

Baseline and three-month De Ritis ratio and gamma-glutamyltransferase as prognostic biomarkers in metastatic renal cell carcinoma treated with targeted therapy.

Oktay Halit Aktepe, Tugce Ulasli, Ilkay Tugba Unek, Elif Atag, Huseyin Salih Semiz, Aziz Karaoglu, Mustafa Erman, Suayib Yalcin

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Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Oktay Halit AktepeDepartment of Medical Oncology, Dokuz Eylul University, Izmir, 35330, Turkey. oktayhalit.aktepe@deu.edu.tr.ORCID https://orcid.org/0000-0003-3540-0701
Tugce UlasliDepartment of Medical Oncology, Dokuz Eylul University, Izmir, 35330, Turkey.
Ilkay Tugba UnekDepartment of Medical Oncology, Dokuz Eylul University, Izmir, 35330, Turkey.
Elif AtagDepartment of Medical Oncology, Dokuz Eylul University, Izmir, 35330, Turkey.
Huseyin Salih SemizDepartment of Medical Oncology, Dokuz Eylul University, Izmir, 35330, Turkey.
Aziz KaraogluDepartment of Medical Oncology, Dokuz Eylul University, Izmir, 35330, Turkey.
Mustafa ErmanDepartment of Medical Oncology, Hacettepe University Cancer Institute, Ankara, Turkey.
Suayib YalcinDepartment of Medical Oncology, Hacettepe University Cancer Institute, Ankara, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Liver function tests (LFTs)–derived parameters such as the De Ritis ratio (DRR) and gamma-glutamyltransferase (GGT) may reflect tumor biology and systemic inflammation. Thus, we evaluated both baseline and 3-month measurements of LFTs in patients with metastatic renal cell carcinoma (mRCC) receiving first-line targeted therapy (TT). We retrospectively analyzed 264 patients with mRCC treated with first-line TT. Progression-free survival (PFS) and overall survival (OS) were estimated by Kaplan–Meier and compared using the log-rank test. Associations of clinicopathological variables with PFS and OS were analyzed using univariate and multivariate Cox models. The median PFS and OS times for the cohort were 12.3 months (95% confidence interval [CI]: 10.7–13.8) and 45.6 months (95% CI: 38.4–52.9), respectively. At 3 months, patients with high DRR had inferior PFS (11.5 vs. 13.4 months, p = 0.003) and OS (33.0 vs. 63.0 months, p < 0.001) compared with those with low DRR. Similarly, patients with elevated GGT (> upper limit of normal) demonstrated shorter PFS (10.3 vs. 13.8 months, p < 0.001) and OS (39.4 vs. 55.0 months, p < 0.001). In multivariate analyses, high DRR was an independent predictor of shorter PFS (hazard ratio [HR]: 1.504, 95% CI: 1.126–2.009, p = 0.006) and OS (HR: 2.108, 95% CI: 1.449–3.066, p < 0.001). Elevated GGT was also independently associated with inferior PFS (HR: 1.624, 95% CI: 1.221–2.158, p < 0.001) and OS (HR: 1.661, 95% CI: 1.198–2.303, p = 0.002). Elevated DRR and GGT values at 3 months were independent predictors of inferior PFS and OS in mRCC, underscoring their utility as practical biomarkers that may improve risk stratification in routine clinical care.

Indexed as

Biomarkers, TumorCarcinoma, Renal Cellgamma-GlutamyltransferaseKidney NeoplasmsAdultAgedFemaleHumansKaplan-Meier EstimateLiver Function TestsMaleMiddle AgedMolecular Targeted TherapyNeoplasm MetastasisPrognosisProgression-Free SurvivalBiomarkers, Tumorgamma-GlutamyltransferaseDe Ritis ratioGamma-glutamyltransferaseGGTLiver function testsMetastatic renal cell carcinoma

Identifiers

PMID41813880
PMCPMC13100095

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.