Severity: Warning
Message: file_get_contents(https://...@gmail.com&api_key=61f08fa0b96a73de8c900d749fcb997acc09&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 197
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 197
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 271
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3165
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 597
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 511
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 317
Function: require_once
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In breast cancer management, predicting axillary lymph node (ALN) metastasis using whole-slide images (WSIs) of primary tumor biopsies is a challenging and underexplored task for pathologists. We developed METACANS, an multimodal artificial intelligence (AI) model that integrates WSIs with clinicopathological features to predict ALN metastasis. METACANS was trained on 1991 cases and externally validated across five cohorts with a total of 2166 cases. Across all validation cohorts, METACANS achieved an area under the curve (AUC) of 0.733 (95% CI, 0.711-0.755), with an overall negative predictive value of 0.846, sensitivity of 0.820, specificity of 0.504, and balanced accuracy of 0.662. Without additional annotations, METACANS identified pathological imaging patterns linked to metastatic status, such as micropapillary growth, infiltrative patterns, and necrosis. While its predictive performance may not yet support immediate clinical application, METACANS addresses the task of predicting ALN metastasis using WSIs and clinicopathological features, and demonstrates the feasibility of multimodal AI approaches for preoperative axillary staging in breast cancer.
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Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12056209 | PMC |
http://dx.doi.org/10.1038/s41698-025-00914-9 | DOI Listing |