Evidence map›Paper›PMID 40429664›Full record

ArticleInternational journal of molecular sciences2025

Clinical Validation of Plasma Metabolite Markers for Early Lung Cancer Detection.

Lun Zhang, Jiamin Zheng, Rashid A Bux, Jean-François Haince, Claudia Torres-Calzada, Rupasri Mandal, Andrew Maksymiuk, Guoyu Huang, Paramjit S Tappia, Philippe Joubert and 2 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. 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

12 authors.

Lun ZhangThe Metabolomics Innovation Centre, University of Alberta, Edmonton, AB T6G 2E8, Canada.
Jiamin ZhengThe Metabolomics Innovation Centre, University of Alberta, Edmonton, AB T6G 2E8, Canada.
Rashid A BuxBioMark Diagnostics Inc., Richmond, BC V6X 2W2, Canada.
Jean-François HainceBioMark Diagnostics Inc., Richmond, BC V6X 2W2, Canada.ORCID 0009-0002-5261-9967
Claudia Torres-CalzadaDepartment of Biological Sciences, University of Alberta, Edmonton, AB T6G 2E8, Canada.
Rupasri MandalThe Metabolomics Innovation Centre, University of Alberta, Edmonton, AB T6G 2E8, Canada.
Andrew MaksymiukCancer Care Manitoba, Winnipeg, MB R3E 0V9, Canada.
Guoyu HuangBioMark Diagnostics Inc., Richmond, BC V6X 2W2, Canada.ORCID 0009-0004-5854-9482
Paramjit S TappiaAsper Clinical Research Institute, St. Boniface Hospital, Winnipeg, MB R2H 2A6, Canada.ORCID 0000-0001-8307-2760
Philippe JoubertInstitut Universitaire de Cardiologie et de Pneumologie de Québec-Université Laval, Quebec, QC G1V 4G5, Canada.ORCID 0000-0001-7784-6387
Christian D RolfoDepartment of Internal Medicine, Division of Medical Oncology, The Arthur G. James Comprehensive Cancer Center, 460 W 12th Avenue, Columbus, OH 43210, USA.
David S WishartThe Metabolomics Innovation Centre, University of Alberta, Edmonton, AB T6G 2E8, Canada.ORCID 0000-0002-3207-2434

Funding

Medteq (Impact Program), Province of Quebec, Canada N/A
6 · The paper itself

Abstract

Early detection of lung cancer significantly improves survival, yet current screening methods have limitations. This study aimed to identify a robust panel of plasma metabolites for early-stage non-small cell lung cancer (NSCLC) diagnosis using a large, clinically diverse patient cohort. A total of 680 archived plasma samples from biopsy-confirmed NSCLC patients and controls (including healthy individuals and patients with non-cancerous lung diseases) were analyzed using targeted, quantitative mass spectrometry-based metabolomics and used as the discovery cohort. An independent set of 216 plasma samples served as the validation cohort. Logistic regression (LR) models developed from the discovery set using ten metabolites achieved area under the receiver-operating characteristic curve (AUROC) values of 93.63%, 93.74%, and 93.91% for distinguishing all-stage, stage I-II, and stage I NSCLC patients from controls, respectively. Incorporating smoking history further improved model performance. The validation cohort confirmed the model's robustness, demonstrating high sensitivity and specificity for early-stage detection. These results support the potential of metabolomic biomarkers as a minimally invasive, accurate tool for early NSCLC diagnosis. This approach may complement current screening methods, enabling earlier intervention and improved patient outcomes. Further studies are warranted to validate these findings in more diverse populations and real-world clinical settings.

Indexed as

Biomarkers, TumorCarcinoma, Non-Small-Cell LungEarly Detection of CancerLung NeoplasmsMetabolomicsAdultAgedCase-Control StudiesFemaleHumansMaleMetabolomeMiddle AgedNeoplasm StagingROC CurveBiomarkers, Tumorearly detectionmetabolite markersnon-small cell lung cancer

Identifiers

PMID40429664
PMCPMC12111207

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.