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Development and validation of an early diagnosis model for bone metastasis in non-small cell lung cancer based on serological characteristics of the bone metastasis mechanism.

作者信息

Teng Xiaoyan, Han Kun, Jin Wei, Ma Liru, Wei Lirong, Min Daliu, Chen Libo, Du Yuzhen

机构信息

Department of Laboratory Medicine, Shanghai Sixth People's Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai 200233, China.

Department of Oncology, Shanghai Sixth People's Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai 200233, China.

出版信息

EClinicalMedicine. 2024 Apr 26;72:102617. doi: 10.1016/j.eclinm.2024.102617. eCollection 2024 Jun.


DOI:10.1016/j.eclinm.2024.102617
PMID:38707910
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11066529/
Abstract

BACKGROUND: Bone metastasis significantly impact the prognosis of non-small cell lung cancer (NSCLC) patients, reducing their quality of life and shortening their survival. Currently, there are no effective tools for the diagnosis and risk assessment of early bone metastasis in NSCLC patients. This study employed machine learning to analyze serum indicators that are closely associated with bone metastasis, aiming to construct a model for the timely detection and prognostic evaluation of bone metastasis in NSCLC patients. METHODS: The derivation cohort consisted of 664 individuals with stage IV NSCLC, diagnosed between 2015 and 2018. The variables considered in this study included age, sex, and 18 specific serum indicators that have been linked to the occurrence of bone metastasis in NSCLC. Variable selection used multivariate logistic regression analysis and Lasso regression analysis. Six machine learning methods were utilized to develop a bone metastasis diagnostic model, assessed with Area Under the Curve (AUC), Decision Curve Analysis (DCA), sensitivity, specificity, and validation cohorts. External validation used 113 NSCLC patients from the Medical Alliance (2019-2020). Furthermore, a prospective validation study was conducted on a cohort of 316 patients (2019-2020) who were devoid of bone metastasis, and followed-up for at least two years to assess the predictive capabilities of this model. The model's prognostic value was evaluated using Kaplan-Meier survival curves. FINDINGS: Through variable selection, 11 serum indictors were identified as independent predictive factors for NSCLC bone metastasis. Six machine learning models were developed using age, sex, and these serum indicators. A random forest (RF) model demonstrated strong performance during the training and internal validation cohorts, achieving an AUC of 0.98 (95% CI 0.95-0.99) for internal validation. External validation further confirmed the RF model's effectiveness, yielding an AUC of 0.97 (95% CI 0.94-0.99). The calibration curves demonstrated a high level of concordance between the anticipated risk and the observed risk of the RF model. Prospective validation revealed that the RF model could predict the occurrence of bone metastasis approximately 10.27 ± 3.58 months in advance, according to the results of the SPECT. An online computing platform (https://bonemetastasis.shinyapps.io/shiny_cls_1model/) for this RF model is publicly available and free-to-use by doctors and patients. INTERPRETATION: This study innovatively employs age, gender, and 11 serological markers closely related to the mechanism of bone metastasis to construct an RF model, providing a reliable tool for the early screening and prognostic assessment of bone metastasis in NSCLC patients. However, as an exploratory study, the findings require further validation through large-scale, multicenter prospective studies. FUNDING: This work is supported by the National Natural Science Foundation of China (NO.81974315); Shanghai Municipal Science and Technology Commission Medical Innovation Research Project (NO.20Y11903300); Shanghai Municipal Health Commission Health Industry Clinical Research Youth Program (NO.20204Y034).

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a96/11066529/b23edbfc2187/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a96/11066529/498a05639759/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a96/11066529/cb2d6b91edf9/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a96/11066529/3522abadb0f4/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a96/11066529/55d193928417/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a96/11066529/6594f508e62a/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a96/11066529/516dfd162ce0/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a96/11066529/b23edbfc2187/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a96/11066529/498a05639759/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a96/11066529/cb2d6b91edf9/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a96/11066529/3522abadb0f4/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a96/11066529/55d193928417/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a96/11066529/6594f508e62a/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a96/11066529/516dfd162ce0/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a96/11066529/b23edbfc2187/gr7.jpg

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本文引用的文献

[1]
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Lancet. 2023-2-4

[2]
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Application of Machine Learning Techniques to Predict Bone Metastasis in Patients with Prostate Cancer.

Cancer Manag Res. 2021-11-23

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Int J Gen Med. 2021-11-3

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Establishment of a regression model of bone metabolism markers for the diagnosis of bone metastases in lung cancer.

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Clinical and inflammatory features based machine learning model for fatal risk prediction of hospitalized COVID-19 patients: results from a retrospective cohort study.

Ann Med. 2021-12

[10]
Bone metastasis: mechanisms, therapies, and biomarkers.

Physiol Rev. 2021-7-1

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