Evidence map›Paper›PMID 42312604›Full record

ArticleBiomolecules & biomedicine2026

Prognostic value of preoperative mGPS, CAR, and NLR in patients undergoing resection for non-small cell lung cancer.

Mehmet Mermer, Hıdır Esme

Abstract read
In one paragraph

Article in Biomolecules & biomedicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–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

1 citing paper in PubMed.

  1. 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

2 authors.

Mehmet MermerDepartment of Chest Diseases, Konya City Hospital, Konya, Türkiye.
Hıdır EsmeDepartment of Thoracic Surgery, Konya City Hospital, Konya, Türkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Systemic inflammation is increasingly recognized as a crucial prognostic factor in non-small cell lung cancer (NSCLC). However, comprehensive evaluations comparing multiple inflammation-based indices in surgically treated cohorts, especially across specific time-dependent survival endpoints, remain scarce. This retrospective observational cohort study analyzed 270 NSCLC patients who underwent surgical resection of the primary tumor within the Konya City Hospital healthcare network. Preoperative inflammatory indices calculated included C-reactive protein to albumin ratio (CAR), neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), platelet-to-albumin ratio (PAR), and modified Glasgow Prognostic Score (mGPS). We assessed overall survival and time-specific survival at 1, 2, and 5 years. Group comparisons were conducted based on survival status at each time point, utilizing univariate and multivariable logistic regression to identify factors associated with time-specific survival. The mean age of the cohort was 71.64 ± 9.71 years, with 78.9% being male. Lobectomy was the most frequent procedure (72.6%). During follow-up, 145 patients died (overall mortality rate of 53.7%). Among these, the mean time from surgery to death was 32.63 ± 23.83 months. Survival rates at 1, 2, and 5 years were 90.0%, 79.3%, and 53.3%, respectively. Inflammatory indices were consistently elevated in non-survivors across all evaluated time points. In multivariable models, CAR and high mGPS status were independently associated with reduced 1-year survival. At 2 years, CAR and high mGPS status maintained their independent association with diminished survival, while NLR demonstrated borderline significance. For 5-year survival, high mGPS status and NLR remained independently associated with reduced survival. Unadjusted analyses revealed a graded association between mGPS and survival. Our findings indicate that preoperative systemic inflammation, particularly elevated mGPS status, CAR, and NLR, is associated with mortality at multiple postoperative time points following NSCLC resection. These results underscore the potential prognostic utility of readily available inflammation-based biomarkers and necessitate further validation through prospective investigations.

Indexed as

Carcinoma, Non-Small-Cell LungC-Reactive ProteinLung NeoplasmsLymphocytesNeutrophilsAgedAged, 80 and overFemaleHumansInflammationMaleMiddle AgedPreoperative PeriodPrognosisRetrospective StudiesC-Reactive Protein

Identifiers

PMID42312604
PMCPMC13667955

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Registered trials

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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.