Evidence map›Paper›PMID 38555313›Full record

ArticleScientific reports2024

The prognostic value and model construction of inflammatory markers for patients with non-small cell lung cancer.

Wanting Xu, Xinya Liu, Ci Yan, Gulinurayi Abdurahmane, Jiayina Lazibiek, Yan Zhang, Mingqin Cao

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

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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

10 citing papers in PubMed.

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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

7 authors.

Wanting Xu *Department of Epidemiology and Health Statistics, School of Public Health, Xinjiang Medical University, Urumqi, 830000, People's Republic of China.
Xinya Liu *The Affiliated Tumor Hospital, Xinjiang Medical University, Urumqi, 830000, People's Republic of China.
Ci YanThe Affiliated Tumor Hospital, Xinjiang Medical University, Urumqi, 830000, People's Republic of China.
Gulinurayi AbdurahmaneDepartment of Epidemiology and Health Statistics, School of Public Health, Xinjiang Medical University, Urumqi, 830000, People's Republic of China.
Jiayina LazibiekDepartment of Epidemiology and Health Statistics, School of Public Health, Xinjiang Medical University, Urumqi, 830000, People's Republic of China.
Yan ZhangDepartment of Epidemiology and Health Statistics, School of Public Health, Xinjiang Medical University, Urumqi, 830000, People's Republic of China.
Mingqin CaoDepartment of Epidemiology and Health Statistics, School of Public Health, Xinjiang Medical University, Urumqi, 830000, People's Republic of China. cmq66@126.com.

Funding

Natural Science Foundation of Xinjiang Uygur Autonomous Region 2022D01C288
6 · The paper itself

Abstract

The aim of this study was to investigate and analyse the predictive value of systemic inflammatory markers based on peripheral blood biomarkers for the prognosis of non-small cell lung cancer (NSCLC) patients. Based on a retrospective monitoring cohort of 973 NSCLC patients from an Affiliated Tumor Hospital from 2012 to 2023. The log-rank test and Cox proportional risk regression model were used to identify independent prognostic inflammatory markers. Subsequently, a nomogram prediction model was constructed and evaluated. The results of multivariate Cox regression analysis showed that patients with high NLR group (HR = 1.238, 95% CI 1.015-1.510, P = 0.035), and high CAR group (HR = 1.729, 95% CI 1.408-2.124, P < 0.001) were risk factors affecting the prognosis of NSCLC patients. The nomogram that includes age, tumor stage, smoking history, BMI, NLR, and CAR can effectively predict the prognosis of NSCLC patients.The inflammatory markers NLR and CAR, which combine inflammatory and nutritional status, are effective predictors of the prognosis of NSCLC patients. The combination of clinical information and these easily accessible inflammatory markers has significant research value for prognostic assessment, clinical treatment, and follow-up monitoring of NSCLC patients.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsHumansNeutrophilsPrognosisRetrospective Studies

Identifiers

PMID38555313
PMCPMC10981730

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