Evidence map›Paper›PMID 40813948›Full record

ArticleDiscover oncology2025

Competing risk model for prognosis of small cell neuroendocrine lung carcinoma based on SEER database.

Dongxu Xia, Jun Fan, Xin Zhou, Fengzhou Li, Fachen Zhou

Abstract read
In one paragraph

Article in Discover oncology, 2025. 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Dongxu Xia *Department of Thoracic Surgery, The First Affiliated Hospital, Dalian Medical University, Dalian, China.
Jun Fan *Department of Thoracic Surgery, The First Affiliated Hospital, Dalian Medical University, Dalian, China.
Xin ZhouDepartment of Histology and Embryology, Dalian Medical University, Dalian, China.
Fengzhou LiDepartment of Thoracic Surgery, The First Affiliated Hospital, Dalian Medical University, Dalian, China. lifengzhou1990@163.com.
Fachen ZhouDepartment of Thoracic Surgery, The First Affiliated Hospital, Dalian Medical University, Dalian, China. zhoufachen@DMU.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn recent years, the incidence of small cell neuroendocrine lung carcinoma (SCNLC) shows an upward trend. Yet there is still a lack of competing risk models for SCNLC. Therefore, this study aims to establish a competing risk model to predict the specific mortality of patients with SCNLC.

methodsPatients diagnosed with SCNLC from 2000 to 2018 were selected from the Surveillance, Epidemiology, and End Results (SEER) database. Univariate and multivariable Fine-Gray regression models were used to select independent predictors of SCNLC-specific mortality. A competing risk model was constructed to predict the cumulative 3- and 5-year specific mortality of SCNLC. C-index, ROC curve, and calibration curve were used for internal validation, and the clinical utility was evaluated by decision curve analysis.

resultsA total of 27,758 patients were included in the analysis. The results of feature selection showed that patient’s age, race, marital status, tumor grade, histology, size, stage, and number of tumors were independent risk factors for specific death of patients. The factor that had the greatest impact on SCNLC-specific mortality was stage IV tumor (HR [95%]: 1.51 [1.31, 1.73]; P < 0.0001), followed by brain metastasis among distant metastases (HR [95%]: 1.37 [1.25, 1.49]; P < 0.0001). Based on the model’s C-index and the area under the ROC curve (AUC), the results indicate that this model can effectively predict SCNLC-specific mortality and has good clinical value.

conclusionThe competing risk model for patients with SCNLC was successfully established and validated internally. The validation results suggest that the model is accurate and practical in the prediction of SCNLC-specific mortality and plays an important role in clinical decision-making and health management for patients with SCNLC.

Indexed as

Competing-risks modelFine‐garyLung cancerPrognostic factorsSEER database

Identifiers

PMID40813948
PMCPMC12354436

What Socratic holds

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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 Socratic graph.