AI Article Synopsis

  • PD-L1 is now recognized as a crucial biomarker for predicting responses to immunotherapy in breast cancer, but current methods for measuring it through immunohistochemistry are expensive and inconsistent.
  • Researchers have developed a deep learning approach to predict PD-L1 expression by analyzing standard H&E-stained images, which are commonly used in cancer diagnosis.
  • In a study of 3,376 patients, the new system demonstrated high predictive accuracy, validated on multiple datasets, and can also identify cases at risk of misinterpretation by pathologists, enhancing clinical decision-making and quality assurance.

Article Abstract

Programmed death ligand-1 (PD-L1) has been recently adopted for breast cancer as a predictive biomarker for immunotherapies. The cost, time, and variability of PD-L1 quantification by immunohistochemistry (IHC) are a challenge. In contrast, hematoxylin and eosin (H&E) is a robust staining used routinely for cancer diagnosis. Here, we show that PD-L1 expression can be predicted from H&E-stained images by employing state-of-the-art deep learning techniques. With the help of two expert pathologists and a designed annotation software, we construct a dataset to assess the feasibility of PD-L1 prediction from H&E in breast cancer. In a cohort of 3,376 patients, our system predicts the PD-L1 status in a high area under the curve (AUC) of 0.91 - 0.93. Our system is validated on two external datasets, including an independent clinical trial cohort, showing consistent prediction performance. Furthermore, the proposed system predicts which cases are prone to pathologists miss-interpretation, showing it can serve as a decision support and quality assurance system in clinical practice.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9643479PMC
http://dx.doi.org/10.1038/s41467-022-34275-9DOI Listing

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