Evidence map›Paper›PMID 38736010›Full record

ArticleScientific reports2024

Unlocking the complete blood count as a risk stratification tool for breast cancer using machine learning: a large scale retrospective study.

Daniella Castro Araujo, Bruno Aragão Rocha, Karina Braga Gomes, Daniel Noce da Silva, Vinicius Moura Ribeiro, Marco Aurelio Kohara, Fernanda Tostes Marana, Renata Andrade Bitar, Adriano Alonso Veloso, Maria Carolina Pintao and 4 more

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

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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

14 authors.

Daniella Castro AraujoHuna, São Paulo, Brazil. danicastroaraujo@gmail.com.ORCID 0000-0002-2748-4776
Bruno Aragão RochaGrupo Fleury, São Paulo, Brazil.
Karina Braga GomesDepartamento de Análises Clínicas e Toxicológicas, Faculdade de Farmácia, Universidade Federal de Minas Gerais/UFMG, Campus Belo Horizonte, Minas Gerais, Brazil.
Daniel Noce da SilvaHuna, São Paulo, Brazil.
Vinicius Moura RibeiroHuna, São Paulo, Brazil.
Marco Aurelio KoharaHuna, São Paulo, Brazil.
Fernanda Tostes MaranaHuna, São Paulo, Brazil.
Renata Andrade BitarHuna, São Paulo, Brazil.
Adriano Alonso VelosoDepartamento de Ciências da Computação, Instituto de Ciências Exatas, Universidade Federal de Minas Gerais/UFMG, Campus Belo Horizonte, Minas Gerais, Brazil.
Maria Carolina PintaoGrupo Fleury, São Paulo, Brazil.
Flavia Helena da SilvaGrupo Fleury, São Paulo, Brazil.
Celso Ferraz VianaGrupo Fleury, São Paulo, Brazil.
Pedro Henrique Araújo de SouzaHuna, São Paulo, Brazil.
Ismael Dale Cotrim Guerreiro da SilvaGrupo Fleury, São Paulo, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Optimizing early breast cancer (BC) detection requires effective risk assessment tools. This retrospective study from Brazil showcases the efficacy of machine learning in discerning complex patterns within routine blood tests, presenting a globally accessible and cost-effective approach for risk evaluation. We analyzed complete blood count (CBC) tests from 396,848 women aged 40-70, who underwent breast imaging or biopsies within six months after their CBC test. Of these, 2861 (0.72%) were identified as cases: 1882 with BC confirmed by anatomopathological tests, and 979 with highly suspicious imaging (BI-RADS 5). The remaining 393,987 participants (99.28%), with BI-RADS 1 or 2 results, were classified as controls. The database was divided into modeling (including training and validation) and testing sets based on diagnostic certainty. The testing set comprised cases confirmed by anatomopathology and controls cancer-free for 4.5-6.5 years post-CBC. Our ridge regression model, incorporating neutrophil-lymphocyte ratio, red blood cells, and age, achieved an AUC of 0.64 (95% CI 0.64-0.65). We also demonstrate that these results are slightly better than those from a boosting machine learning model, LightGBM, plus having the benefit of being fully interpretable. Using the probabilistic output from this model, we divided the study population into four risk groups: high, moderate, average, and low risk, which obtained relative ratios of BC of 1.99, 1.32, 1.02, and 0.42, respectively. The aim of this stratification was to streamline prioritization, potentially improving the early detection of breast cancer, particularly in resource-limited environments. As a risk stratification tool, this model offers the potential for personalized breast cancer screening by prioritizing women based on their individual risk, thereby indicating a shift from a broad population strategy.

Indexed as

Breast NeoplasmsMachine LearningAdultAgedBlood Cell CountBrazilEarly Detection of CancerFemaleHumansMiddle AgedRetrospective StudiesRisk AssessmentBreast cancerCBCCBC-ratiosHemogramMachine learningNLRRBCRisk stratificationRoutine blood testsScreening

Identifiers

PMID38736010
PMCPMC11089041

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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.