Brianna Munnich , Haowen Zhou , Mark Watson , Cory Bernadt , Steven (Siyu) Lin , Jon Ritter , Chieh-Yu Lin , Ramaswamy Govindan , Siddarth Rawal , Changhuei Yang , Richard Cote
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引用次数: 0
Abstract
Brain metastases can occur in nearly half of patients with early and locally advanced (stage I-III) non-small cell lung cancer (NSCLC). There are no reliable histopathologic or molecular means to identify those who are likely to develop brain metastases. We sought to determine if deep learning (DL) could be applied to routine hematoxylin and eosin (H&E) stained primary tumor tissue sections from Stage I-III NSCLC patients to predict the development of brain metastasis. Diagnostic slides from 158 patients with Stage I to III NSCLC followed for at least 5 years for development of brain metastases (Met+, 65 patients) versus no progression (Met-, 93 patients) were subjected to whole slide imaging. Three separate iterations of DL were performed by first selecting 118 cases (45 Met+, 73 Met-) to train and validate the DL algorithm, while 40 separate cases (20 Met+, 20 Met-) were used as the test set. DL algorithm results were compared to a blinded review by four expert pathologists. The DL-based algorithm was able to distinguish eventual development of brain metastases with an accuracy of 87% (p<0.0001) compared to an average of 57.3% by the four pathologists, and appears to be particularly useful in predicting brain metastases in Stage I patients. DL-based algorithms using routine H&E-stained slides may identify patients likely to develop brain metastases from those that will remain disease free over extended (>5 year) follow-up and may thus be spared systemic therapy.
期刊介绍:
The aim of Cancer Genetics is to publish high quality scientific papers on the cellular, genetic and molecular aspects of cancer, including cancer predisposition and clinical diagnostic applications. Specific areas of interest include descriptions of new chromosomal, molecular or epigenetic alterations in benign and malignant diseases; novel laboratory approaches for identification and characterization of chromosomal rearrangements or genomic alterations in cancer cells; correlation of genetic changes with pathology and clinical presentation; and the molecular genetics of cancer predisposition. To reach a basic science and clinical multidisciplinary audience, we welcome original full-length articles, reviews, meeting summaries, brief reports, and letters to the editor.