Evidence map›Paper›PMID 40507370›Full record

ReviewCancers2025

Effectiveness of Artificial Intelligence Models in Predicting Lung Cancer Recurrence: A Gene Biomarker-Driven Review.

Niloufar Pourakbar, Alireza Motamedi, Mahta Pashapour, Mohammad Emad Sharifi, Seyedemad Seyedgholami Sharabiani, Asra Fazlollahi, Hamid Abdollahi, Arman Rahmim, Sahar Rezaei

Abstract readReview
In one paragraph

Review in Cancers, 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. Review
  3. Article
  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

9 authors.

Niloufar PourakbarStudent Research Committee, Tabriz University of Medical Sciences, Tabriz 5165665931, Iran.
Alireza MotamediStudent Research Committee, Tabriz University of Medical Sciences, Tabriz 5165665931, Iran.
Mahta PashapourStudent Research Committee, Tabriz University of Medical Sciences, Tabriz 5165665931, Iran.
Mohammad Emad SharifiShariati Hospital Research Center, Tehran University of Medical Sciences, Tehran 1416634793, Iran.ORCID 0000-0003-2846-6964
Seyedemad Seyedgholami SharabianiStudent Research Committee, Tabriz University of Medical Sciences, Tabriz 5165665931, Iran.
Asra FazlollahiStudent Research Committee, Tabriz University of Medical Sciences, Tabriz 5165665931, Iran.
Hamid AbdollahiResearch Department of Integrative Oncology, BC Cancer Institute, Vancouver, BC V5Z 1L3, Canada.ORCID 0000-0003-0761-1309
Arman RahmimResearch Department of Integrative Oncology, BC Cancer Institute, Vancouver, BC V5Z 1L3, Canada.ORCID 0000-0002-9980-2403
Sahar RezaeiDepartment of Radiology, Medical School, Tabriz University of Medical Sciences, Tabriz 5165665931, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

objectivesLung cancer recurrence, particularly in NSCLC, remains a major challenge, with 30-70% of patients relapsing post-treatment. Traditional predictors like TNM staging and histopathology fail to account for tumor heterogeneity and immune dynamics. This review evaluates AI models integrating gene biomarkers (TP53, KRAS, FOXP3, PD-L1, and CD8) to enhance the recurrence prediction and improve the personalized risk stratification.

methodsFollowing the PRISMA guidelines, we systematically reviewed AI-driven recurrence prediction models for lung cancer, focusing on genomic biomarkers. Studies were selected based on predefined criteria, emphasizing AI/ML approaches integrating gene expression, radiomics, and clinical data. Data extraction covered the study design, AI algorithms (e.g., neural networks, SVM, and gradient boosting), performance metrics (AUC and sensitivity), and clinical applicability. Two reviewers independently screened and assessed studies to ensure accuracy and minimize bias.

resultsA literature analysis of 18 studies (2019-2024) from 14 countries, covering 4861 NSCLC and small cell lung cancer patients, showed that AI models outperformed conventional methods. AI achieved AUCs of 0.73-0.92 compared to 0.61 for TNM staging. Multi-modal approaches integrating gene expression (PDIA3 and MYH11), radiomics, and clinical data improved accuracy, with SVM-based models reaching a 92% AUC. Key predictors included immune-related signatures (e.g., tumor-infiltrating NK cells and PD-L1 expression) and pathway alterations (NF-κB and JAK-STAT). However, small cohorts (41-1348 patients), data heterogeneity, and limited external validation remained challenges.

conclusionsAI-driven models hold potential for recurrence prediction and guiding adjuvant therapies in high-risk NSCLC patients. Expanding multi-institutional datasets, standardizing validation, and improving clinical integration are crucial for real-world adoption. Optimizing biomarker panels and using AI trustworthily and ethically could enhance precision oncology, enabling early, tailored interventions to reduce mortality.

Indexed as

artificial intelligenceclinical integrationgene biomarkerslung cancer recurrencepredictive models

Identifiers

PMID40507370
PMCPMC12153899

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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.