Efficacy of three lung cancer prediction models in diagnosing benign and malignant pulmonary nodules.

IF 1.5 4区 医学 Q4 ONCOLOGY
Translational cancer research Pub Date : 2025-04-30 Epub Date: 2025-04-27 DOI:10.21037/tcr-2025-468
Hesen Wu, Xingyi Chen, Xiaoming Feng, Wei He, Duilio Divisi, Jimmy T Efird, José Franco, Xuemin Guo
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引用次数: 0

Abstract

Background: The predictive models for malignant lung nodules have been developed, but need further validation and optimization for broader clinical use. This study aimed to compare the diagnostic efficacy of the Mayo model, Peking University People's Hospital (PKUPH) model, and the lung cancer biomarker panel (LCBP) model in distinguishing between benign and malignant pulmonary nodules, providing valuable clinical research data for the early diagnosis of lung cancer.

Methods: Clinical and imaging data of patients diagnosed with pulmonary nodules at Meizhou People's Hospital from March 2021 through January 2023 were collected. Data from patients with benign pulmonary nodules during the same period, who served as negative referents, were also gathered. The Mayo model, PKUPH model, and LCBP model were used to clinically validate lung cancer prediction rates. The receiver operating characteristic (ROC) curves and statistical significance comparing the areas under the curve (AUCs) for each model were evaluated.

Results: A total of 428 patients were included: 160 females and 268 males. The noncancer group included 218 cases (50.93%), and the cancer group included 210 cases (49.07%). The AUC values of the three models were as follows: Mayo model, 0.783; PKUPH model, 0.726; and LCBP model, 0.759. (I) For the Mayo model, at the maximum Youden index, the concordance rate was 74.3%, the sensitivity 85.71%, the specificity 63.30%, the positive predictive value 69.23%, the negative predictive value 82.14%, the positive likelihood ratio 2.335, and the negative likelihood ratio 0.226. (II) For the PKUPH model, at the maximum Youden index, the concordance rate was 70.3%, the sensitivity 84.29%, the specificity 56.88%, the positive predictive value 65.31%, the negative predictive value 78.98%, the positive likelihood ratio 1.955, and the negative likelihood ratio 0.276. (III) For the LCBP model, at the maximum Youden index, the concordance rate was 75.0%, the sensitivity 72.38%, the specificity 77.52%, the positive predictive value 75.62%, the negative predictive value 74.45%, the positive likelihood ratio 3.220, and the negative likelihood ratio 0.356.

Conclusions: All three predictive models exhibit clinical applicability, with minimal differences in diagnostic efficacy. The LCBP model outperformed both the Mayo and PKUPH models in diagnostic performance, showing greater diagnostic value for the Chinese population. However, there is still room for optimization in each model.

三种肺癌预测模型对良恶性肺结节的诊断效果。
背景:恶性肺结节的预测模型已经建立,但为了更广泛的临床应用,还需要进一步的验证和优化。本研究旨在比较Mayo模型、北京大学人民医院(PKUPH)模型和肺癌生物标志物面板(LCBP)模型对肺结节良恶性的诊断效果,为肺癌的早期诊断提供有价值的临床研究数据。方法:收集2021年3月至2023年1月梅州人民医院诊断为肺结节患者的临床和影像学资料。同时也收集了同期良性肺结节患者的数据,作为阴性对照。采用Mayo模型、PKUPH模型和LCBP模型进行肺癌预测率的临床验证。评估各模型的受试者工作特征(ROC)曲线及曲线下面积(auc)比较的统计学意义。结果:共纳入428例患者,其中女性160例,男性268例。非癌组218例(50.93%),癌组210例(49.07%)。3种模型的AUC值分别为:Mayo模型,0.783;PKUPH模型,0.726;LCBP模型,0.759。(1) Mayo模型在最大约登指数下,符合率为74.3%,敏感性为85.71%,特异性为63.30%,阳性预测值为69.23%,阴性预测值为82.14%,阳性似然比为2.335,阴性似然比为0.226。(II) PKUPH模型在最大约登指数下,符合率为70.3%,敏感性84.29%,特异性56.88%,阳性预测值65.31%,阴性预测值78.98%,阳性似然比1.955,阴性似然比0.276。(III) LCBP模型在最大约登指数下,符合率为75.0%,敏感性72.38%,特异性77.52%,阳性预测值75.62%,阴性预测值74.45%,阳性似然比3.220,阴性似然比0.356。结论:三种预测模型均具有临床适用性,诊断效果差异极小。LCBP模型的诊断性能优于Mayo和PKUPH模型,对中国人群显示出更大的诊断价值。然而,每个模型仍有优化的空间。
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来源期刊
CiteScore
2.10
自引率
0.00%
发文量
252
期刊介绍: Translational Cancer Research (Transl Cancer Res TCR; Print ISSN: 2218-676X; Online ISSN 2219-6803; http://tcr.amegroups.com/) is an Open Access, peer-reviewed journal, indexed in Science Citation Index Expanded (SCIE). TCR publishes laboratory studies of novel therapeutic interventions as well as clinical trials which evaluate new treatment paradigms for cancer; results of novel research investigations which bridge the laboratory and clinical settings including risk assessment, cellular and molecular characterization, prevention, detection, diagnosis and treatment of human cancers with the overall goal of improving the clinical care of cancer patients. The focus of TCR is original, peer-reviewed, science-based research that successfully advances clinical medicine toward the goal of improving patients'' quality of life. The editors and an international advisory group of scientists and clinician-scientists as well as other experts will hold TCR articles to the high-quality standards. We accept Original Articles as well as Review Articles, Editorials and Brief Articles.
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