Multicenter study develops a model combining genomic and pathological features, improving prediction of PFS and OS in NSCLC.
Although immunotherapy combined with chemotherapy (ICT) is the standard treatment for advanced non-small cell lung cancer (NSCLC), identification of reliable prognostic biomarkers remains challenging. In this multicenter study, we performed next-generation sequencing of tumor samples from 162 patients receiving first-line ICT at the Chinese PLA General Hospital and collected their pathological image information. First, we established a model to predict the risk of tumor progression based on genomic characteristics. Furthermore, a deep learning method was employed to recognize different cell types from pathological images, which significantly improved the accuracy of progression-free survival (PFS) and overall survival (OS) prediction. In summary, we constructed a Prognostic Multimodal Classifier for Progression (PMCP) that possesses the capability to precisely forecast PFS and OS. Patients with the PMCP1 subtype exhibit a low risk of progression and demonstrate a higher proportion of epithelial cells. PMCP highlighted the potential value of multimodal biomarkers in guiding clinical decisions regarding ICT. The area under curve (AUC) for predicting PFS was 0.807. This study revealed the importance of integrating genomic and pathological data to improve prognostic accuracy and enable personalized treatment for patients with advanced NSCLC.
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Han et al. (2025) studied this question.
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