Evidence map›Paper›PMID 41251828›Full record

ArticleInternational journal of colorectal disease2025

AI-driven pre-screening for colorectal cancer using complete blood counts: toward broader population impact.

Bruna Los, Bruno Aragão Rocha, Daniel Noce da Silva, Vinicius Moura Ribeiro, Marco Aurelio Kohara, Rodrigo Azevedo Rodrigues, Maria Carolina Tostes Pintão, Otavio Jose Eulalio Pereira, João Vicente de Morais Malvezzi, Flavia Helena da Silva and 2 more

Abstract read
In one paragraph

Article in International journal of colorectal disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Bruna Los, Huna, São Paulo, Brazil.
Bruno Aragão RochaGrupo Fleury, São Paulo, Brazil.
Daniel Noce da Silva, Huna, São Paulo, Brazil.
Vinicius Moura Ribeiro, Huna, São Paulo, Brazil.
Marco Aurelio Kohara, Huna, São Paulo, Brazil.
Rodrigo Azevedo RodriguesGrupo Fleury, São Paulo, Brazil.
Maria Carolina Tostes PintãoGrupo Fleury, São Paulo, Brazil.
Otavio Jose Eulalio PereiraGrupo Fleury, São Paulo, Brazil.
João Vicente de Morais MalvezziGrupo Fleury, São Paulo, Brazil.
Flavia Helena da SilvaGrupo Fleury, São Paulo, Brazil.
Pedro Henrique Araújo de Souza, Huna, São Paulo, Brazil.
Daniella Castro Araújo, Huna, São Paulo, Brazil. dani@huna.ai.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeEarly colorectal cancer (CRC) detection is crucial for effective treatment; however, traditional screening methods face challenges. Colonoscopy, though highly effective, has limited availability, and fecal immunochemical tests (FIT) are more accessible and cost-effective but suffer from low adherence. Our retrospective study aimed to develop a transparent artificial-intelligence model leveraging routine CBC data as a cost-effective method for CRC detection.

methodsWe conducted a retrospective analysis of 28,450 individuals aged 45-75 who underwent colonoscopy within six months of a complete blood count (CBC) test. Among them, 439 (1.8%) had CRC, 2,955 (11.8%) had advanced adenomas, and 21,662 (86.5%) had benign findings on colonoscopy. The database was divided into training (70%) and testing (30%) sets. The model was developed using ridge regression.

resultsDescriptive analysis revealed significant differences between CRC cases and controls across most CBC markers, CBC-derived ratios, and age (P < 0.001), except for lymphocytes. The model, based on red cell distribution width (RDW), systemic inflammation response index (SIRI), hemoglobin, and age, achieved an AUC of 0.77 (95% CI: 0.75-0.77) for CRC, comparable to a deep learning model (TabPFN). Interpretability analysis revealed that older age, elevated RDW and SIRI, and low hemoglobin were associated with CRC. In a subgroup (7.25%) with FIT results, FIT showed higher sensitivity for CRC (88%) than the model (64%), but lower specificity (77% vs. 81%).

conclusionGiven CBC's widespread use and accessibility, this approach may be a scalable pre-screening tool to improve CRC risk stratification and optimize resource allocation, demonstrating how explainable AI may augment existing CRC screening programs.

Indexed as

Artificial IntelligenceColorectal NeoplasmsEarly Detection of CancerAgedBlood Cell CountColonoscopyFemaleHumansMaleMiddle AgedRetrospective StudiesArtificial intelligenceColorectal cancerInterpretable AIMachine learningReal-world dataRisk stratification

Identifiers

PMID41251828
PMCPMC12627115

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LicenceCC BY-NC-ND
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Registered trials

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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.