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Review
. 2021 Jul 13;11(1):14358.
doi: 10.1038/s41598-021-93746-z.

CAD systems for colorectal cancer from WSI are still not ready for clinical acceptance

Affiliations
Review

CAD systems for colorectal cancer from WSI are still not ready for clinical acceptance

Sara P Oliveira et al. Sci Rep. .

Abstract

Most oncological cases can be detected by imaging techniques, but diagnosis is based on pathological assessment of tissue samples. In recent years, the pathology field has evolved to a digital era where tissue samples are digitised and evaluated on screen. As a result, digital pathology opened up many research opportunities, allowing the development of more advanced image processing techniques, as well as artificial intelligence (AI) methodologies. Nevertheless, despite colorectal cancer (CRC) being the second deadliest cancer type worldwide, with increasing incidence rates, the application of AI for CRC diagnosis, particularly on whole-slide images (WSI), is still a young field. In this review, we analyse some relevant works published on this particular task and highlight the limitations that hinder the application of these works in clinical practice. We also empirically investigate the feasibility of using weakly annotated datasets to support the development of computer-aided diagnosis systems for CRC from WSI. Our study underscores the need for large datasets in this field and the use of an appropriate learning methodology to gain the most benefit from partially annotated datasets. The CRC WSI dataset used in this study, containing 1,133 colorectal biopsy and polypectomy samples, is available upon reasonable request.

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Conflict of interest statement

The authors declare no competing interests.

Figures

Figure 1
Figure 1
Digital pathology workflow, from collecting the biopsy sample to the WSI visualisation.
Figure 2
Figure 2
Normal colonic mucosa and dysplastic progression.
Figure 3
Figure 3
Example of a whole-slide (a) from the CRC dataset. Manual segmentations (b) include regions annotated as non-neoplastic (white), low-grade lesions (blue), high-grade lesions (pink), linfocytes (green) and fulguration (yellow).
Figure 4
Figure 4
Slide classes distribution on CRC dataset.
Figure 5
Figure 5
Proposed workflow for colorectal cancer diagnosis on whole-slide images.
Figure 6
Figure 6
Performance evaluated on CRC dataset.

References

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