ArticleNPJ digital medicine2026
Soft multiclass feature augmented deep learning to predict tumor origins using cytology or histology whole slide images.
Article in NPJ digital medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
1 citing paper in PubMed.
- Few-Shot Learning for Cytological Classification of Primary Lung Cancer and Pulmonary Metastases During Endobronchial Ultrasound.Diagnostics (Basel, Switzerland) · 2026Article
Corrections and comments
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Authors and funding
6 authors.
Funding
Abstract
Tailoring cancer treatment to the primary tumor site is essential for optimal outcomes, yet identifying the source of metastasis remains a significant clinical challenge. The primary tumor location influences not only the choice of treatment but also its delivery method, potential side effects and overall prognosis. Cancer of unknown primary (CUP) persists despite comprehensive diagnostic evaluations. We present the first fast, low-cost deep learning based cancer screening approach, i.e. a new data efficient soft multiclass feature augmentation deep learning, to identify the primary origin of malignant cells directly from whole slide images (WSIs) of cytological smears (CS), cell blocks (CB) or histopathology slides. Our framework was evaluated across three datasets: a multi-center histopathology collection of 69 sites (1,196 WSIs), a CS dataset (260 WSIs), and a CB dataset (129 WSIs). The proposed method achieved excellent accuracy, outperforming four state-of-the-art methods in identifying common metastatic origins. These findings demonstrate the potential of this deep learning tool to advance precision oncology by rapidly guiding clinicians toward appropriate, site-specific cancer treatments.
Identifiers
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.