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H&E-based Computational Biomarker Enables Universal EGFR Screening for Lung Adenocarcinoma

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arxiv 2206.10573 v1 pith:UFOITU45 submitted 2022-06-21 cs.CV q-bio.QM

classification cs.CVq-bio.QM
keywords lungegfrcancerclinicalpatientstestingadenocarcinomacomputational
verification ladder T0 review T1 audit T2 compute T3 formal
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Lung cancer is the leading cause of cancer death worldwide, with lung adenocarcinoma being the most prevalent form of lung cancer. EGFR positive lung adenocarcinomas have been shown to have high response rates to TKI therapy, underlying the essential nature of molecular testing for lung cancers. Despite current guidelines consider testing necessary, a large portion of patients are not routinely profiled, resulting in millions of people not receiving the optimal treatment for their lung cancer. Sequencing is the gold standard for molecular testing of EGFR mutations, but it can take several weeks for results to come back, which is not ideal in a time constrained scenario. The development of alternative screening tools capable of detecting EGFR mutations quickly and cheaply while preserving tissue for sequencing could help reduce the amount of sub-optimally treated patients. We propose a multi-modal approach which integrates pathology images and clinical variables to predict EGFR mutational status achieving an AUC of 84% on the largest clinical cohort to date. Such a computational model could be deployed at large at little additional cost. Its clinical application could reduce the number of patients who receive sub-optimal treatments by 53.1% in China, and up to 96.6% in the US.

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Cited by 2 Pith papers

Reviewed papers in the Pith corpus that reference this work. Sorted by Pith novelty score.

  1. Identifying actionable driver mutations in lung cancer using an efficient Asymmetric Transformer Decoder

    eess.IV 2025-08 unverdicted novelty 5.0 of 10

    The authors propose an Asymmetric Transformer Decoder that uses tissue type and patch embeddings to predict six actionable lung cancer mutations from H&E slides, but the uploaded full text is a different document.

  2. Pathology Foundation Models are Scanner Sensitive: Benchmark and Mitigation with Contrastive ScanGen Loss

    q-bio.QM 2025-07 conditional novelty 5.0 of 10

    Pathology foundation models produce scanner-dependent predictions, and the ScanGen contrastive loss reduces this scanner bias during fine-tuning for EGFR mutation prediction from whole slide images.

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