Evidence map›Paper›PMID 40673105›Full record

ArticleTranslational lung cancer research2025

An explainable AI approach to surgical and radiotherapy interventions for optimized treatment decision-making in early-stage non-small cell lung cancer.

Qunzhe Ding, Chendong Wang, Zhe Zhang, Junjie Liao, Lufan Tang, Jiade Jay Lu, Zhibo Tan

Abstract read
In one paragraph

Article in Translational lung cancer research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–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

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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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.

Qunzhe Ding *School of Information Management, Wuhan University, Wuhan, China.ORCID https://orcid.org/0009-0002-2615-6049
Chendong Wang *Hepatic Surgery Center, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Zhe ZhangDepartment of Radiation Oncology, Peking University Shenzhen Hospital, Shenzhen, China.
Junjie LiaoDepartment of Radiation Oncology, Proton and Heavy Ion Center, Heyou Hospital, Heyou International Health System, Foshan, China.
Lufan TangDepartment of Radiation Oncology, Proton and Heavy Ion Center, Heyou Hospital, Heyou International Health System, Foshan, China.
Jiade Jay Lu *Department of Radiation Oncology, Proton and Heavy Ion Center, Heyou Hospital, Heyou International Health System, Foshan, China.
Zhibo Tan *Department of Radiation Oncology, Proton and Heavy Ion Center, Heyou Hospital, Heyou International Health System, Foshan, China.ORCID https://orcid.org/0000-0002-9673-1371

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: For individual patients with early-stage non-small cell lung cancer (NSCLC), robust evidence to guide treatment selection between surgery and stereotactic body radiotherapy (SBRT) remains limited. This study aimed to develop machine learning-driven predictive models using the Surveillance, Epidemiology, and End Results (SEER) database to evaluate the efficacy of these treatments, thereby providing a data-driven foundation for personalized treatment decisions. Methods: Stage I or IIA NSCLC patients diagnosed between 2012 and 2018 were identified from the SEER database. Six machine learning models, spanning from classical to advanced approaches, were employed to predict 1-, 3-, and 5-year survival, with their performance assessed using seven metrics. The SHAP (SHapley Additive exPlanations) interpretability method was employed to explain the optimal predictive model, focusing on analyzing the differences between surgical and radiotherapy treatments under various factors, providing valuable insights to optimizing treatment strategies. Patients diagnosed between 2019 and 2021 were selected as an external validation cohort to assess the generalizability and robustness of the previously developed models. Results: A total of 26,566 patients were included in the training and internal testing cohort of the study. LightGBM (light gradient boosting machine) outperformed other models across most metrics for survival predictions. The SHAP interpretability analysis revealed that tumor location, tumor size, pathology, and treatment type were significant factors for 3- and 5-year predictions. Furthermore, at 3- and 5-year intervals, the efficacy of radiotherapy was comparable to surgery for left upper lobe tumors, while radiotherapy appeared slightly inferior to surgery for right lower lobe tumors. Meanwhile, for tumors <1.5 cm or 3.5-5 cm, lobectomy exhibited the best efficacy, while for tumors measuring 1.5-3.5 cm, the efficacy of lobectomy seemed to be slightly inferior to radiotherapy and sublobar resection. For adenocarcinoma and squamous cell carcinoma, radiotherapy and lobectomy could be regarded as the preferred treatment methods, respectively. Besides, for patients <45 or >75 years old, sublobar resection showed the best efficacy at the 5-year interval. The external validation cohort of 11,927 patients further confirmed the effectiveness of the models in predicting 1-, 3-, and 5-year survival outcomes, reinforcing their reliability and applicability in clinical decision-making. Conclusions: This study provides valuable insights into treatment decision-making for stages I and IIA NSCLC. The LightGBM model is a reliable tool for survival prediction for early-stage NSCLC. By utilizing this model, it can be concluded that tumor location, tumor size, pathological type and age are vital factors significantly influencing the choice of treatment methods.

Indexed as

machine learningNon-small cell lung cancer (NSCLC)SHAP interpretabilitystereotactic body radiotherapy (SBRT)surgery

Identifiers

PMID40673105
PMCPMC12261364

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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 OpenQuestion graph.