余坤興博士現任哈佛醫學院生物醫學資訊學系副教授。他開發出首個可從全玻片病理影像中自動擷取大量特徵的人工智慧演算法,並透過研究揭示腫瘤細胞顯微表型背後的分子機制,發現可預測病人預後的新型細胞形態。
余教授實驗室結合多體學資料與量化病理影像分析,用於預測癌症病人的臨床表現。其團隊開發的 AI 病理方法已獲全球超過 200 個研究實驗室獨立驗證。
他在 AI 病理領域貢獻卓著,曾獲 NIH MIRA 獎、Google Research Scholar Award、AMIA New Investigator Award、哈佛醫學院 Dean’s Innovation Award、美國國防部 Career Development Award,以及美國癌症學會 Research Scholar Award,並為美國醫學資訊學會院士(FAMIA)。
Kun-Hsing "Kun" Yu, M.D., Ph.D., is an Associate Professor in the Department of Biomedical Informatics at Harvard Medical School. He pioneered the first fully automated artificial intelligence (AI) algorithm capable of extracting thousands of features from whole-slide pathology images. His research has uncovered molecular mechanisms driving the microscopic phenotypes of tumor cells and identified novel cellular morphologies that predict patient prognosis.
Dr. Yu's lab integrates multi-omics (e.g., genomics, epigenomics, transcriptomics, and proteomics) profiles with quantitative pathology patterns to predict clinical phenotypes in cancer patients. The AI methods developed by the Yu Lab have been independently validated by over 200 research laboratories worldwide.
His contributions to AI in pathology have earned numerous honors, including the National Institutes of Health (NIH) Maximizing Investigators' Research Award, Google Research Scholar Award, American Medical Informatics Association New Investigator Award, Harvard Medical School Dean's Innovation Award, Department of Defense (DoD) Career Development Award, and the American Cancer Society (ACS) Research Scholar Award. He is a Fellow of the American Medical Informatics Association (FAMIA).
Abstract:
Artificial intelligence (AI) is rapidly reshaping the landscape of cancer pathology research and clinical practice. Recent advances in high-resolution whole-slide image digitization, large-scale data curation, multi-modal machine learning algorithms, and scalable computing infrastructure have enabled the development of AI systems capable of learning directly from raw histopathology images at an unprecedented scale. These innovations allow models to capture both fine-grained cellular morphology and higher-order tissue architecture, linking visual patterns to clinical outcomes. As a result, pathology is evolving from a largely qualitative discipline into a data-rich, quantitative science, where reproducible and scalable computational methods can augment human interpretation. This transformation is opening new opportunities for biomarker discovery, risk stratification, and precision oncology, while also raising important questions about generalizability and reliability in real-world deployment.
In this talk, I will present a unified framework for next-generation pathology AI centered on three key pillars: scale, safety, and social responsibility. First, I will highlight recent progress in pathology foundation models that leverage weakly supervised and self-supervised learning to extract generalizable representations from tens of thousands of whole-slide images spanning multiple cancer types and clinical settings. By learning from heterogeneous datasets without requiring exhaustive manual annotations, these models can capture shared and disease-specific morphological features that transfer across tasks. They enable a wide range of downstream applications, including tumor detection, subtype classification, molecular characterization, and prognostic prediction, while demonstrating robustness to variations in staining, scanning, and sample preparation across institutions and populations.
Second, I will discuss advances in uncertainty-aware AI systems designed to enhance the safety and reliability of clinical decision-making. By integrating Bayesian inference, deep ensembles, and distribution-aware modeling techniques, these approaches provide calibrated estimates of prediction confidence and explicitly quantify different sources of uncertainty. Importantly, they can identify out-of-distribution cases, such as rare tumor types or diagnostically ambiguous samples, and flag them for further expert review. Such capabilities are essential for high-stakes clinical applications, where overconfident errors can lead to inappropriate treatment decisions and adverse patient outcomes.
Third, I will introduce emerging methods for fairness-aware pathology AI that explicitly address performance disparities across demographic groups and healthcare settings. Using contrastive learning and large-scale multi-cohort analyses, these approaches learn representations that are less sensitive to spurious correlations while preserving clinically relevant biological signals. They substantially reduce performance gaps across subpopulations and provide new insights into how biological heterogeneity, such as differences in somatic mutation prevalence, and data imbalance jointly contribute to variability in AI performance.
Finally, I will outline key challenges and future directions in building robust, generalizable, and clinically deployable AI systems, including issues of transportability across populations, interpretability of complex models, rigorous external validation, and seamless integration into clinical workflows. Together, these ongoing advances point toward a new paradigm in pathology, where AI not only augments diagnosis but also drives scientific discovery, democratizes access to high-quality clinical care, and supports safer and more informed decision-making.