ArticleOncology letters2026
Real-world performance of the machine learning-based prediction of chemotherapy-associated adverse effects in lung cancer.
Article in Oncology letters, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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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.
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.
Who cites it
1 citing paper in PubMed.
- Akiferidin suppresses cervical cancer growth and angiogenesis via the VEGF/DLL4-Notch pathway.Frontiers in pharmacology · 2026Article
Corrections and comments
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Authors and funding
9 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Systemic chemotherapy is the cornerstone for treating patients with locally advanced non-small-cell lung cancer (NSCLC). Various adverse effects (AEs) are caused by anticancer therapy, limiting the efficacy of chemotherapy. The precise prediction and early detection of AEs could result in improved efficacy of chemotherapy and quality of life. In the present study, machine learning (ML) algorithms, including random forest (RF), multilayer perceptron and AdaBoost, were employed to develop prediction models for common AEs using dynamic treatment information. A total of 1,659 chemotherapeutic information data points for 403 patients with NSCLC who underwent chemotherapy were extracted from an electronic health record system. A five-fold cross-validation was performed, and the received operating characteristic (ROC) curve and calibration curve were used to evaluate the model performance. Patients with multi-AEs had worse therapeutic efficacy of neoadjuvant chemotherapy (P<0.001; Fisher's exact test) and worse prognosis (P<0.05; log-rank test) compared with patients without multi-AEs. The area under ROC curve values of the RF model were 0.75, 0.74 and 0.76 for predicting myelosuppression, low albumin and hepatic impairment, respectively, and its calibration curve was found linear in the calibration range with regression factor r
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Registered trials
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