Evidence map›Paper›PMID 39858018›Full record

ArticleCancers2025

Enhancing Treatment Decisions for Advanced Non-Small Cell Lung Cancer with Epidermal Growth Factor Receptor Mutations: A Reinforcement Learning Approach.

Hakan Şat Bozcuk, Leyla Sert, Muhammet Ali Kaplan, Ali Murat Tatlı, Mustafa Karaca, Harun Muğlu, Ahmet Bilici, Bilge Şah Kılıçtaş, Mehmet Artaç, Pınar Erel and 16 more

Abstract read
In one paragraph

Article in Cancers, 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. 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

26 authors.

Hakan Şat BozcukIndependent Researcher, Antalya 07100, Turkey.
Leyla SertDepartment of Medical Oncology, Dicle University, Diyarbakır 21280, Turkey.
Muhammet Ali KaplanDepartment of Medical Oncology, Dicle University, Diyarbakır 21280, Turkey.
Ali Murat TatlıDepartment of Medical Oncology, Akdeniz University, Antalya 07058, Turkey.
Mustafa KaracaDepartment of Medical Oncology, Akdeniz University, Antalya 07058, Turkey.
Harun MuğluDepartment of Medical Oncology, Faculty of Medicine, İstanbul Medipol University, İstanbul 34810, Turkey.ORCID 0000-0001-9584-0827
Ahmet BiliciDepartment of Medical Oncology, Faculty of Medicine, İstanbul Medipol University, İstanbul 34810, Turkey.ORCID 0000-0002-0443-6966
Bilge Şah KılıçtaşDepartment of Medical Oncology, Necmettin Erbakan University, Konya 42090, Turkey.
Mehmet ArtaçDepartment of Medical Oncology, Necmettin Erbakan University, Konya 42090, Turkey.
Pınar ErelDepartment of Medical Oncology, Marmara University, İstanbul 34722, Turkey.
Perran Fulden YumukDepartment of Medical Oncology, Marmara University, İstanbul 34722, Turkey.ORCID 0000-0001-8650-299X
Burak BilginFaculty of Medicine, Ankara Yıldırım Beyazıt University, Ankara 06010, Turkey.
Mehmet Ali Nahit ŞendurFaculty of Medicine, Ankara Yıldırım Beyazıt University, Ankara 06010, Turkey.ORCID 0000-0001-7021-6139
Saadettin KılıçkapDepartment of Medical Oncology, Faculty of Medicine, İstinye University, İstanbul 34010, Turkey.
Hakan TabanDepartment of Medical Oncology, Medical Park Keçiören Hospital, Ankara 06120, Turkey.ORCID 0000-0002-2004-7741
Sevinç BallıDepartment of Medical Oncology, Ankara University, Ankara 06100, Turkey.
Ahmet DemirkazıkDepartment of Medical Oncology, Ankara University, Ankara 06100, Turkey.ORCID 0000-0002-2917-7999
Fatma AkdağDepartment of Medical Oncology, Sakarya University, Sakarya 54050, Turkey.
İlhan HacıbekiroğluDepartment of Medical Oncology, Sakarya University, Sakarya 54050, Turkey.ORCID 0000-0002-0333-7405
Halil Göksel GüzelAntalya Education and Research Hospital, Antalya 07100, Turkey.
Murat KoçerAntalya Education and Research Hospital, Antalya 07100, Turkey.
Pınar GürsoyDepartment of Medical Oncology, Ege University, İzmir 35040, Turkey.
Bahadır KöylüDivision of Medical Oncology, School of Medicine, Koç University, İstanbul 34450, Turkey.ORCID 0000-0002-4462-6393
Fatih SelçukbiricikDivision of Medical Oncology, School of Medicine, Koç University, İstanbul 34450, Turkey.
Gökhan KarakayaDepartment of Medical Oncology, ASV Yaşam Hospital, Antalya 07300, Turkey.ORCID 0000-0002-7970-307X
Mustafa Serkan AlemdarDepartment of Medical Oncology, Faculty of Medicine, İstinye University, İstanbul 34010, Turkey.ORCID 0000-0002-7663-6182

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlthough higher-generation TKIs are associated with improved progression-free survival in advanced NSCLC patients with EGFR mutations, the optimal selection of TKI treatment remains uncertain. To address this gap, we developed a web application powered by a reinforcement learning (RL) algorithm to assist in guiding initial TKI treatment decisions.

methodsClinical and mutational data from advanced NSCLC patients were retrospectively collected from 14 medical centers. Only patients with complete data and sufficient follow-up were included. Multiple supervised machine learning models were tested, with the Extra Trees Classifier (ETC) identified as the most effective for predicting progression-free survival. Feature importance scores were calculated by the ETC, and features were then integrated into a Deep Q-Network (DQN) RL algorithm. The RL model was designed to select optimal TKI generation and a treatment line for each patient and was embedded into an open-source web application for experimental clinical use.

resultsIn total, 318 cases of EGFR-mutant advanced NSCLC were analyzed, with a median patient age of 63. A total of 52.2% of patients were female, and 83.3% had ECOG scores of 0 or 1. The top three most influential features identified were neutrophil-to-lymphocyte ratio (log-transformed), age (log-transformed), and the treatment line of TKI administration, as tested by the ETC algorithm, with an area under curve (AUC) value of 0.73, whereas the DQN RL algorithm achieved a higher AUC value of 0.80, assigning distinct Q-values across four TKI treatment categories. This supports the decision-making process in the web-based 'EGFR Mutant NSCLC Treatment Advisory System', where clinicians can input patient-specific data to receive tailored recommendations.

conclusionsThe RL-based web application shows promise in assisting TKI treatment selection for EGFR-mutant advanced NSCLC patients, underscoring the potential for reinforcement learning to enhance decision-making in oncology care.

Indexed as

artificial intelligencedeep learningepidermal growth factor receptormachine learningmutationnon-small cell lung cancertyrosine kinase inhibitors

Identifiers

PMID39858018
PMCPMC11763509

What OpenQuestion 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 OpenQuestion graph.