Background The AI-HOPE Lung Cancer study is a multicenter initiative designed to integrate artificial intelligence (AI) and real-world data to improve outcome prediction in patients with metastatic non-small-cell lung cancer treated with first-line immunotherapy-based regimens. AI-HOPE aims to leverage machine learning (ML) models to generate individualized predictions of progression-free survival (PFS), overall survival (OS), and treatment-related toxicity in a broad, unselected population. Materials and methods Clinical and imaging data are harmonized and stored within a privacy-compliant infrastructure (San Raffaele Ai CEnter [S-RACE] platform), promoting FAIR (Findable, Accessible, Interoperable and Reusable) data principles and minimizing manual workload. The primary objective is the development of time-to-event models for PFS and OS. Complementary binary classification models will explore early progression, long-term survival, and clinically relevant toxicities. Results The study includes retrospective (from 2017) and prospective (until 2027) phases across 21 European centers. So far, 920 patients have been recruited for the study, of whom 621 have baseline imaging scans available for centralized analysis. In the AI-HOPE study, a flexible methodological approach integrates multiple ML models tailored to specific clinical questions, complemented by explainable AI tools. Multimodal models combining clinical variables with computed tomography and [18F]2-fluoro-2-deoxy-d-glucose–positron emission tomography imaging features (when available) are supported through the S-RACE platform, which provides a partially automated imaging analysis workflow. Conclusions By combining structured clinical variables and multimodal imaging data, the AI-HOPE Lung Cancer study aims to support refined risk stratification and treatment personalization, ultimately facilitating the responsible integration of AI into routine thoracic oncology practice.
F. Ogliari, M. Ferrara, J. Huijs et al.· ESMO real world data and dig...· 0 citations
ABSTRACT Introduction The discovery of epidermal growth factor receptor (EGFR) mutations has deeply reshaped the treatment of non-small cell lung cancer (NSCLC). Throughout the last years, third-generation tyrosine kinase inhibitor (TKI) osimertinib in monotherapy has been the standard of care; however, resistance limits durable responses, necessitating novel combinations and sequencing strategies. Areas covered This review discusses recent advances in EGFR-targeted therapies within the molecular landscape of classical and uncommon EGFR mutations, focusing on frontline intensification strategies in metastatic disease—specifically TKI combinations with chemotherapy (FLAURA2) or bispecific antibodies (MARIPOSA)—and emerging post-progression strategies to overcome acquired resistance mechanisms. A comprehensive literature search (January 2021–March 2026) was conducted via PubMed, and recent major oncology conference proceedings (ASCO, ESMO, WCLC, ELCC) and clinical trial registries for ongoing studies. Expert opinion The therapeutic landscape is shifting from a uniform frontline TKI monotherapy approach toward biomarker-driven, risk-stratified, intensification. High-risk patients (e.g. TP53 co-mutations, L858R) derive significant benefit from combination regimens, whereas mono-TKI remains appropriate for favorable prognostic subgroups. Future progress relies on validating predictive biomarkers—particularly circulating tumor DNA (ctDNA) dynamics—to guide adaptive treatment strategies, balancing efficacy gains against toxicity and costs, while ensuring equitable global access to novel therapies.
L. Lucente, Lucrezia Barcellini, B. Ramella Pollone et al.· Expert Opinion on Pharmacoth...· 0 citations