Evidence map›Paper›PMID 40468278›Full record

ArticleBMC cancer2025

Identification and validation of a DNA methylation-block prognostic model in non-small cell lung cancer patients.

Hang Li, Yi Lu, Haiqing Chen, Tong Li, Fangqiu Fu, Jing Wang, Bing Li, Hong Hu

Abstract readValidation Study
In one paragraph

Article in BMC cancer, 2025. 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. Review
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

8 authors.

Hang Li *Departments of Thoracic Surgery, State Key Laboratory of Genetic Engineering, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Yi Lu *Burning Rock Biotech, Guangzhou, 510300, China.
Haiqing ChenDepartments of Thoracic Surgery, State Key Laboratory of Genetic Engineering, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Tong LiDepartments of Thoracic Surgery, State Key Laboratory of Genetic Engineering, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Fangqiu FuDepartments of Thoracic Surgery, State Key Laboratory of Genetic Engineering, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Jing WangBurning Rock Biotech, Guangzhou, 510300, China.
Bing LiBurning Rock Biotech, Guangzhou, 510300, China.
Hong HuDepartments of Thoracic Surgery, State Key Laboratory of Genetic Engineering, Fudan University Shanghai Cancer Center, Shanghai, 200032, China. huhong0997@163.com.

Funding

National Natural Science Foundation of China 82003285
6 · The paper itself

Abstract

backgroundDuring perioperative care for non-small cell lung cancer (NSCLC) patients, clinical outcomes vary significantly. There is a critical need for more dependable biomarkers to identify high-risk individuals in the perioperative phase. This is essential for enhancing postoperative interventions and positively influencing clinical results.

methodWe collected a tissue DNA methylation cohort of 73 stage I-III surgically treated patients as the discovery set for model development. The model was established using recurrence-free survival (RFS) as the primary endpoint. Subsequently, its prognostic value was validated in an independent cohort of 30 stage I-III surgical patients, and further confirmed across different patient subgroups.

resultsWe developed an Early to Mid-term NSCLC Recurrence LASSO score (EMRL) predictive model based on five differentially methylated regions (DMRs). The EMRL model was significantly associated with RFS in stage I-III surgically treated patients (RFS: log-rank P = 0.00032) and was confirmed as an independent prognostic factor in multivariate Cox regression analysis (HR = 0.35, 95% confidence interval 0.20-0.61, P < 0.001). Notably, EMRL not only identified high-risk patients within the same TNM stage but also demonstrated strong predictive performance in patient subgroups harboring EGFR-TKI-sensitive mutations and those with positive PD-L1 expression.

conclusionIn this study, we developed a postoperative recurrence prediction model based on preoperative tissue methylation characteristics to identify individuals in I-III stage NSCLC patients following surgical resection who may have a higher risk of recurrence. This offers opportunities for early personalized treatment and follow-up strategy.

Indexed as

Biomarkers, TumorCarcinoma, Non-Small-Cell LungDNA MethylationLung NeoplasmsNeoplasm Recurrence, LocalAgedFemaleHumansMaleMiddle AgedNeoplasm StagingPrognosisBiomarkers, TumorDifferential methylation regionsDNA methylationNon-small cell lung cancerPostoperative recurrence prediction model

Identifiers

PMID40468278
PMCPMC12135241

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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.