

This study introduces AI‐TFNA, an innovative artificial intelligence model designed to assist cytopathologists in classifying thyroid nodules based on The Bethesda System for Reporting Thyroid Cytopathology (TBSRTC). The model effectively differentiates between benign and malignant thyroid nodules, demonstrating significant potential as a screening tool to enhance diagnostic accuracy and workflow efficiency in clinical practice. Abstract The rising prevalence of thyroid nodules is straining limited cytopathology resources, resulting in excessive overdiagnosis and overtreatment with significant patient and healthcare consequences. To address this, AI‐TFNA is developed, a robust artificial intelligence platform leveraging extensive clinical data to enhance diagnostic accuracy and clinical efficiency. A total of 20,803 thyroid samples are collected from seven medical centers across different regions in China. Of these, 4,421 thyroid fine‐needle aspiration (TFNA) samples from three hospitals are used to train AI‐TFNA, ensuring strong generalizability across diverse clinical settings. For the internal validation, AI‐TFNA demonstrates exceptional performance: the overall accuracy of TBS I is 93.27%, the sensitivity of TBS V and TBS VI reaches 85.37% and 83.78%, while the specificity of TBS II is 97.13%. Consistent results are observed in an external cohort of 2,153 samples, demonstrating robust generalizability. The incorporation of BRAF mutation data into AI‐TFNA and the development of a multi‐modal model further improve precision by significantly improving the differentiation between benign and malignant thyroid nodules. Migration (IAM) is an innovative technique that substantially improves cross‐institutional model generalizability, increasing AI‐TFNA sensitivity by 1.90% and specificity by 8.12%. AI‐TFNA offers rapid, reliable decision support, advancing thyroid nodule diagnostics. This study introduces AI-TFNA, an innovative artificial intelligence model designed to assist cytopathologists in classifying thyroid nodules based on The Bethesda System for Reporting Thyroid Cytopathology (TBSRTC). The model effectively differentiates between benign and malignant thyroid nodules, demonstrating significant potential as a screening tool to enhance diagnostic accuracy and workflow efficiency in clinical practice. Abstract The rising prevalence of thyroid nodules is straining limited cytopathology resources, resulting in excessive overdiagnosis and overtreatment with significant patient and healthcare consequences. To address this, AI-TFNA is developed, a robust artificial intelligence platform leveraging extensive clinical data to enhance diagnostic accuracy and clinical efficiency. A total of 20,803 thyroid samples are collected from seven medical centers across different regions in China. Of these, 4,421 thyroid fine-needle aspiration (TFNA) samples from three hospitals are used to train AI-TFNA, ensuring strong generalizability across diverse clinical settings. For the internal validation, AI-TFNA demonstrates exceptional performance: the overall accuracy of TBS I is 93.27%, the sensitivity of TBS V and TBS VI reaches 85.37% and 83.78%, while the specificity of TBS II is 97.13%. Consistent results are observed in an external cohort of 2,153 samples, demonstrating robust generalizability. The incorporation of BRAF mutation data into AI-TFNA and the development of a multi-modal model further improve precision by significantly improving the differentiation between benign and malignant thyroid nodules. Migration (IAM) is an innovative technique that substantially improves cross-institutional model generalizability, increasing AI-TFNA sensitivity by 1.90% and specificity by 8.12%. AI-TFNA offers rapid, reliable decision support, advancing thyroid nodule diagnostics. Advanced Science, Volume 12, Issue 48, December 29, 2025.
Medical Journal
|15th Jan, 2026
|Nature Medicine's Advance Online Publication (AOP) table of contents.
Medical Journal
|15th Jan, 2026
|Wiley
Medical Journal
|15th Jan, 2026
|Wiley
Medical Journal
|15th Jan, 2026
|Wiley
Medical Journal
|15th Jan, 2026
|Wiley
Medical Journal
|15th Jan, 2026
|Wiley
Medical Journal
|15th Jan, 2026
|Wiley