Evidence map›Paper›PMID 41142828›Full record

ArticleFrontiers in immunology2025

Predicting preoperative lymph node status in patients with cervical cancer: development of interpretable machine learning model and support for the biological plausibility.

Hui Shen, Yuting Jiang, Lihe Zhang, Qiao Zheng, Han Bai, Lihong Wu, Liu Du, Hongning Xie

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Article in Frontiers in immunology, 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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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Hui Shen *Department of Ultrasonic Medicine, Fetal Medical Centre, the First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, Guangdong, China.
Yuting Jiang *Department of Ultrasonic Medicine, Fetal Medical Centre, the First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, Guangdong, China.
Lihe Zhang *Department of Ultrasonic Medicine, Fetal Medical Centre, the First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, Guangdong, China.
Qiao ZhengDepartment of Ultrasonic Medicine, Fetal Medical Centre, the First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, Guangdong, China.
Han BaiDepartment of Ultrasonic Medicine, Fetal Medical Centre, the First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, Guangdong, China.
Lihong WuDepartment of Ultrasonic Medicine, Fetal Medical Centre, the First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, Guangdong, China.
Liu DuDepartment of Ultrasonic Medicine, Fetal Medical Centre, the First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, Guangdong, China.
Hongning XieDepartment of Ultrasonic Medicine, Fetal Medical Centre, the First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, Guangdong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Lymph node metastasis serves as a crucial prognostic risk factor for patients with cervical cancer. Accurate prediction of lymph node metastasis is important in guiding treatment selection. Therefore, our primary objective is the development and validation of machine learning models for predicting lymph node metastasis; the secondary objective is to utilize the sequencing data to provide biological plausibility. Methods: This study retrospectively included 292 cervical cancer patients and prospectively recruited 54 cervical cancer patients. Univariate and multivariate analysis were conducted to explore the risk factors associated with lymph node metastasis. Subsequently, cellular-level validation was performed using single cell RNA-sequencing data. The prognostic value of the risk factor was assessed through bulk RNA-sequencing analysis. Finally, patients were divided into train and retrospective test sets in a 7:3 ratio to develop five machine learning models, while using the prospective test set to validate the models. Additionally, the Shapley Additive Explanation method was employed to enhance the interpretability of the models' decision processes. Results: Federation of Gynecology and Obstetrics stage (2018), squamous cell carcinoma antigen, monocyte count and platelet count were found to be significantly correlated with lymph node metastasis. Meanwhile, monocyte count was a significant risk factor (OR=2.28, Conclusions: This study investigated the notable association between monocyte count and lymph node metastasis, highlighting the importance of monocytes in cervical cancer via bulk RNA-sequencing and single cell RNA-sequencing analysis. The developed interpretable machine learning models effectively aid clinicians in decision-making processes. Additionally, the Shapley Additive Explanation method improved the applicability of these machine learning models in real world.

Indexed as

Lymph NodesMachine LearningUterine Cervical NeoplasmsAdultAgedFemaleHumansLymphatic MetastasisMiddle AgedPrognosisRetrospective StudiesRisk Factorscervical cancerlymph node metastasismachine learningmonocyteSHAP value

Identifiers

PMID41142828
PMCPMC12549587

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