Radwan Qasrawi, Razan AbuGhoush, Ghada Issa, Suliman Thwib, Malak Amro, Rand Al Taweel, Sara Asfour, Yazan Dibas, Tawfiq Abukeshek, Marwan Qubja
Automated CT lung nodule classification suffers from domain shift across centers. We propose LoRA-GRL, combining Low-Rank Adaptation (LoRA) with adversarial domain harmonization via a Gradient Reversal Layer. Rank-8 LoRA modules were inserted into all attention and feed-forward linear projections (48 sites) of a frozen ViT-S backbone; a domain discriminator encouraged center-invariant features across three centers. Normal vs. Benign and Normal vs. Malignant tasks used 264 patients with patient-level five-fold stratified cross-validation. LoRA-GRL achieved AUCs of 0.9735 and 0.9869, close to full fine-tuning (0.9747 and 0.9863). Differences from strongest baselines fell within overlapping 95% CIs under paired bootstrap, indicating comparable discrimination, not superiority. Efficiency is the main advantage: only 0.789 M trainable parameters, a 96.4% reduction from 21.865 M, and inference latency matched full fine-tuning after adapter merging. Grad-CAM showed nodule-localized predictions but also slice-selection failures. For benign classification, higher AUC than plain LoRA came with higher specificity but lower sensitivity. For malignant classification, sensitivity was 0.9412 (5.9 pp above full fine-tuning) and specificity 0.9697. The small cross-center AUC range (0.0011) reflects internal consistency across participating centers, not unseen-site generalization. LoRA-GRL is a promising parameter-efficient candidate for multi-center lung nodule classification, potentially reducing scanner-specific bias and storage/memory needs, but clinical utility requires external validation and prospective evaluation.