Evidence map›Paper›PMID 39873989›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2025

F-18 FDG PET/CT based Preoperative Machine Learning Prediction Models for Evaluating Regional Lymph Node Metastasis Status of Patients with Colon Cancer.

Su Jung Choi, Ji Sun Park, Hyung Joo Baik, Min Sung An, Ki Beom Bae, Sun Seong Lee

Abstract read
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Article in Asian Pacific journal of cancer prevention : APJCP, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Su Jung ChoiDepartment of Nuclear Medicine, Busan Paik Hospital, University of Inje College of Medicine, Busan, Republic of Korea.
Ji Sun ParkDepartment of Nuclear Medicine, Busan Paik Hospital, University of Inje College of Medicine, Busan, Republic of Korea.
Hyung Joo BaikDepartment of Surgery, Busan Paik Hospital, University of Inje College of Medicine, Busan, Republic of Korea.
Min Sung AnDepartment of Surgery, Busan Paik Hospital, University of Inje College of Medicine, Busan, Republic of Korea.
Ki Beom BaeDepartment of Surgery, Busan Paik Hospital, University of Inje College of Medicine, Busan, Republic of Korea.ORCID 0000-0001-7432-9464
Sun Seong LeeDepartment of Nuclear Medicine, Busan Paik Hospital, University of Inje College of Medicine, Busan, Republic of Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThis study aimed to develop a simple machine-learning model incorporating lymph node metastasis status with F-18 Fluorodeoxyglucose positron emission tomography/computed tomography (FDG PET/CT) and clinical information for predicting regional lymph node metastasis in patients with colon cancer.

methodsThis retrospective study included 193 patients diagnosed with colon cancer between January 2014 and December 2017. All patients underwent F-18 FDG PET/CT and blood test before surgery. One categorical variable (lymph node FDG uptake [LNFDG]) and six continuous variables (age, neutrophil-to-lymphocyte ratio [NLR], carcinoembryonic antigen [CEA], carbohydrate antigen 19-9 [CA19-9], C-reactive protein, and maximal standardized uptake value (SUVmax) of the primary tumor) were used as input variables. Four supervised machine learning methods were used to build predictive models: logistic regression (LR), random forest (RF), gradient boosting machine (GBM), and support vector machine (SVM). Area under the receiver operating characteristic curve (AUC) of the validation set were used for evaluating and comparing model performance.

resultsThe number of patients with lymph node metastasis were 63 (33%). The mean number of harvested lymph nodes was 28.8 ± 11.4. The mean CEA, CA19-9, and CRP levels were 4.8 ± 9.3 ng/ml, 15.6 ± 42.8 U/ml, and 1.0 ± 3.0 mg/dl, respectively. The mean NLR was 2.2 ± 1.2. The mean SUVmax levels of the primary tumor were 15.2 ± 7.9. Fifty-one (26%) patients showed FDG uptake in the pericolic lymph nodes.  The mean AUC of the LR, RF, GBM, and SVM methods for the LNFDG model was 0.7046, 0.7047, 0.7040, and 0.7058, respectively. The mean AUC of the LR, RF, GBM, and SVM methods for the LNFDG plus clinical information model was 0.7046, 0.7302, 0.7444, and 0.7097, respectively.

conclusionMachine learning methods using LNFDG and clinical information could predict the lymph node metastasis status in patients with colon cancer with higher accuracy than a model using only FDG uptake of the lymph nodes.

Indexed as

Colonic NeoplasmsFluorodeoxyglucose F18Lymph NodesMachine LearningPositron Emission Tomography Computed TomographyAdultAgedAged, 80 and overFemaleFollow-Up StudiesHumansLymphatic MetastasisMaleMiddle AgedPrognosisRadiopharmaceuticalsFluorodeoxyglucose F18RadiopharmaceuticalsColon cancerF-18 FDG PET/CTLymph node metastasisMachine Learning

Identifiers

PMID39873989
PMCPMC12082408

What Socratic holds

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LicenceCC BY-NC
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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 Socratic graph.