Publication: Enhancing treatment decisions for advanced non-small cell lung cancer with epidermal growth factor receptor mutations: a reinforcement learning approach
| dc.contributor.coauthor | Bozcuk, Hakan Sat | |
| dc.contributor.coauthor | Sert, Leyla | |
| dc.contributor.coauthor | Kaplan, Muhammet Ali | |
| dc.contributor.coauthor | Tatli, Ali Murat | |
| dc.contributor.coauthor | Karaca, Mustafa | |
| dc.contributor.coauthor | Muglu, Harun | |
| dc.contributor.coauthor | Bilici, Ahmet | |
| dc.contributor.coauthor | Kilictas, Bilge Sah | |
| dc.contributor.coauthor | Artac, Mehmet | |
| dc.contributor.coauthor | Erel, Pinar | |
| dc.contributor.coauthor | Bilgin, Burak | |
| dc.contributor.coauthor | Sendur, Mehmet Ali Nahit | |
| dc.contributor.coauthor | Kilickap, Saadettin | |
| dc.contributor.coauthor | Taban, Hakan | |
| dc.contributor.coauthor | Balli, Sevinc | |
| dc.contributor.coauthor | Demirkazik, Ahmet | |
| dc.contributor.coauthor | Akdag, Fatma | |
| dc.contributor.coauthor | Hacibekiroglu, Ilhan | |
| dc.contributor.coauthor | Guzel, Halil Goksel | |
| dc.contributor.coauthor | Kocer, Murat | |
| dc.contributor.coauthor | Gursoy, Pinar | |
| dc.contributor.coauthor | Karakaya, Goekhan | |
| dc.contributor.coauthor | Alemdar, Mustafa Serkan | |
| dc.contributor.department | School of Medicine | |
| dc.contributor.kuauthor | Other, Yumuk, Perran Fulden | |
| dc.contributor.kuauthor | Faculty Member, Selçukbiricik, Fatih | |
| dc.contributor.kuauthor | Doctor, Köylü, Bahadır | |
| dc.contributor.schoolcollegeinstitute | SCHOOL OF MEDICINE | |
| dc.date.accessioned | 2025-05-22T10:36:24Z | |
| dc.date.available | 2025-05-22 | |
| dc.date.issued | 2025 | |
| dc.description.abstract | Background: Although 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. Methods: Clinical 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. Results: In 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. Conclusions: The 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. | |
| dc.description.fulltext | Yes | |
| dc.description.harvestedfrom | Manual | |
| dc.description.indexedby | WOS | |
| dc.description.indexedby | Scopus | |
| dc.description.indexedby | PubMed | |
| dc.description.openaccess | Gold OA | |
| dc.description.publisherscope | International | |
| dc.description.readpublish | N/A | |
| dc.description.sponsoredbyTubitakEu | N/A | |
| dc.description.version | Published Version | |
| dc.identifier.doi | 10.3390/cancers17020233 | |
| dc.identifier.eissn | 2072-6694 | |
| dc.identifier.embargo | No | |
| dc.identifier.filenameinventoryno | IR06320 | |
| dc.identifier.issue | 2 | |
| dc.identifier.quartile | Q2 | |
| dc.identifier.scopus | 2-s2.0-85215677631 | |
| dc.identifier.uri | https://doi.org/10.3390/cancers17020233 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.14288/29573 | |
| dc.identifier.volume | 17 | |
| dc.identifier.wos | 001403762100001 | |
| dc.keywords | Non-small cell lung cancer | |
| dc.keywords | Epidermal growth factor receptor | |
| dc.keywords | Mutation | |
| dc.keywords | Tyrosine kinase inhibitors | |
| dc.keywords | Deep learning | |
| dc.keywords | Machine learning | |
| dc.keywords | Artificial intelligence | |
| dc.language.iso | eng | |
| dc.publisher | MDPI | |
| dc.relation.affiliation | Koç University | |
| dc.relation.collection | Koç University Institutional Repository | |
| dc.relation.ispartof | Cancers | |
| dc.relation.openaccess | Yes | |
| dc.rights | CC BY (Attribution) | |
| dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | |
| dc.subject | Oncology | |
| dc.title | Enhancing treatment decisions for advanced non-small cell lung cancer with epidermal growth factor receptor mutations: a reinforcement learning approach | |
| dc.type | Journal Article | |
| dspace.entity.type | Publication | |
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