ArticleFrontiers in physiology2026
CRC-Former: frequency-domain adaptive swin-transformer for colorectal cancer histopathology classification.
Article in Frontiers in physiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
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.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Introduction: Colorectal cancer (CRC) diagnosis from whole-slide histopathology images remains challenging due to pronounced tissue heterogeneity, multi-scale morphological variations, and the subtle nature of early neoplastic changes. While deep learning models have shown promise, conventional architectures struggle to simultaneously capture fine-grained texture cues and global architectural context, often overlooking diagnostically critical frequency-domain signatures. Methods: To address these limitations, we propose CRC-Former, a novel hybrid architecture that synergistically integrates frequency-aware representation learning with efficient cross-scale sequence modeling. Specifically, CRC-Former introduces two key components: (i) a Frequency-aware Global-Local Transformer Block (FGT), which decomposes features via Haar wavelet transform and applies orientation-specific sliding-window attention in distinct subbands to enhance sensitivity to multi-directional pathological textures; and (ii) a Cross-Scale Mamba Block (CSM), which leverages selective state-space modeling to fuse hierarchical features across resolutions with linear complexity. Results: Evaluated on the large-scale Chaoyang CRC dataset, CRC-Former achieves state-of-the-art performance, outperforming strong baselines. Discussion: Our work demonstrates that explicit integration of signal processing priors with modern sequence modeling offers a powerful paradigm for robust, interpretable, and scalable computational pathology.
Indexed as
Identifiers
What OpenQuestion holds
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 OpenQuestion graph.