4.7 Article

Combining the Fecal Immunochemical Test with a Logistic Regression Model for Screening Colorectal Neoplasia

期刊

FRONTIERS IN PHARMACOLOGY
卷 12, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fphar.2021.635481

关键词

fecal immunochemical test; colorectal neoplasia screening; logistic regression model; funnel strategy; classifier model

资金

  1. Science and Technology Foundation of Shenzhen [JCYJ20180305164128430]
  2. International Cooperation Foundation of Shenzhen [GJHZ20180928171602104]
  3. Shenzhen Economic and Information Committee Innovation Chain and Industry Chain integration special support plan project [20180225112449943]
  4. Shenzhen Public Service Platform on Tumor Precision Medicine and Molecular Diagnosis
  5. Research Grants Council of the Hong Kong Special Administrative Region, China [CityU 21101115, 11102317, 11103718, 11103619, R4017-18, C4041-17GF]
  6. Guangdong Basic and Applied Basic Research Foundation [2019B030302012]
  7. Young Scientists Fund of the National Natural Science Foundation of China [81802384]
  8. International innovation team for early diagnosis and precise treatment of lung cancer [KQTD2016113015442590]

向作者/读者索取更多资源

In this study, a classifier model was established by combining FIT results and other demographic and clinical features to enhance the sensitivity of identifying colorectal neoplasia. The top six features mostly related to CRC include age, gender, history of intestinal adenoma or polyposis, smoking history, gastrointestinal discomfort symptom, and fruit eating habit. The LR algorithm was used to generate the model, achieving an AUC score of 0.92 and an NMSE score of 0.076 in separating normal individuals from participants with colorectal neoplasia.
Background: The fecal immunochemical test (FIT) is a widely used strategy for colorectal cancer (CRC) screening with moderate sensitivity. To further increase the sensitivity of FIT in identifying colorectal neoplasia, in this study, we established a classifier model by combining FIT result and other demographic and clinical features. Methods: A total of 4,477 participants were examined with FIT and those who tested positive (over 100 ng/ml) were followed up by a colonoscopy examination. Demographic and clinical information of participants including four domains (basic information, clinical history, diet habits and life styles) that consist of 15 features were retrieved from questionnaire surveys. A mean decrease accuracy (MDA) score was used to select features that are mostly related to CRC. Five different algorithms including logistic regression (LR), classification and regression tree (CART), support vector machine (SVM), artificial neural network (ANN) and random forest (RF) were used to generate a classifier model, through a 10X cross validation process. Area under curve (AUC) and normalized mean squared error (NMSE) were used in the evaluation of the performance of the model. Results: The top six features that are mostly related to CRC include age, gender, history of intestinal adenoma or polyposis, smoking history, gastrointestinal discomfort symptom and fruit eating habit were selected. LR algorithm was used in the generation of the model. An AUC score of 0.92 and an NMSE score of 0.076 were obtained by the final classifier model in separating normal individuals from participants with colorectal neoplasia. Conclusion: Our results provide a new Funnel strategy in colorectal neoplasia screening via adding a classifier model filtering step between FIT and colonoscopy examination. This strategy minimizes the need of colonoscopy examination while increases the sensitivity of FIT-based CRC screening.

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