Hannah Wilding , Nicholas Mikolajewicz , Debarati Bhanja , Camille Moeckel , Ahmad Ozair , Leonardo de Macedo Filho , Kyle Tuohy , Nima Hamidi , Mara Trifoi , Brianna Snyder , Bailey Kuechenmeister , Schahin Salmanian , Manmeet Ahluwalia , Alireza Mansouri
{"title":"预测非小细胞肺癌患者脑转移发展的nomogram:一项使用常规医疗记录的回顾性分析","authors":"Hannah Wilding , Nicholas Mikolajewicz , Debarati Bhanja , Camille Moeckel , Ahmad Ozair , Leonardo de Macedo Filho , Kyle Tuohy , Nima Hamidi , Mara Trifoi , Brianna Snyder , Bailey Kuechenmeister , Schahin Salmanian , Manmeet Ahluwalia , Alireza Mansouri","doi":"10.1016/j.lana.2025.101213","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>Brain metastases (BrM) are a frequent complication among patients with non-small cell lung cancer (NSCLC). While guidelines exist for baseline CNS screening in advanced NSCLC, surveillance strategies for early-stage disease remain limited. This study aimed to develop a time-dependent BrM risk prediction nomogram using readily available clinical information.</div></div><div><h3>Methods</h3><div>We analyzed a retrospective cohort of NSCLC patients at Penn State Health. Our objectives were to (1) systematically evaluate the performance of existing BrM risk prediction algorithms and (2) construct novel nomograms for BrM risk prediction in NSCLC. Using Cox-proportional hazard models with L1-regularization, we predicted BrM risk at 6-month, 1-year, and 2-year follow-up intervals.</div></div><div><h3>Findings</h3><div>The patient cohort included 1904 patients (median age 68 years, range 38–94 years, BrM incidence 22.8%). The cohort included 1059 males (55.6%) and 845 females (44.4%). Of the cohort, 92.8% of patients identified as White (n = 1766), 1.0% as Asian (n = 19), 4.0% as Black (n = 77), and 2.2% as another race (n = 42). The Zhang 2021 model demonstrated the highest performance in predicting BrM incidence in our cohort, achieving an AUROC of 0.91 (95% CI: 0.87, 0.95). Two novel models were developed: a baseline model incorporating clinical and imaging data at diagnosis (cTNM stage, age at diagnosis), and an extended model including additional clinical and treatment data (number of extracranial metastatic sites, prior radiotherapy, chemotherapy, surgery, and histology) (<span><span>https://nmikolajewicz.shinyapps.io/nomogram_wilding2024/</span><svg><path></path></svg></span>). While both models showed similar short-term performance, the extended model demonstrated superior predictive capacity (AUROC 0.91 at 3-years) for longer-term outcomes. Our nomograms rely exclusively on clinical features routinely documented in patient records, thereby requiring no additional investigations.</div></div><div><h3>Interpretation</h3><div>These clinically accessible nomograms for BrM prediction will facilitate prognostic modeling, risk stratification, refinement of CNS screening guidelines, and patient counseling.</div></div><div><h3>Funding</h3><div>None.</div></div>","PeriodicalId":29783,"journal":{"name":"Lancet Regional Health-Americas","volume":"50 ","pages":"Article 101213"},"PeriodicalIF":7.0000,"publicationDate":"2025-08-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A nomogram to predict development of brain metastasis in non-small cell lung cancer patients: a retrospective analysis using routinely available medical records\",\"authors\":\"Hannah Wilding , Nicholas Mikolajewicz , Debarati Bhanja , Camille Moeckel , Ahmad Ozair , Leonardo de Macedo Filho , Kyle Tuohy , Nima Hamidi , Mara Trifoi , Brianna Snyder , Bailey Kuechenmeister , Schahin Salmanian , Manmeet Ahluwalia , Alireza Mansouri\",\"doi\":\"10.1016/j.lana.2025.101213\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><div>Brain metastases (BrM) are a frequent complication among patients with non-small cell lung cancer (NSCLC). While guidelines exist for baseline CNS screening in advanced NSCLC, surveillance strategies for early-stage disease remain limited. This study aimed to develop a time-dependent BrM risk prediction nomogram using readily available clinical information.</div></div><div><h3>Methods</h3><div>We analyzed a retrospective cohort of NSCLC patients at Penn State Health. Our objectives were to (1) systematically evaluate the performance of existing BrM risk prediction algorithms and (2) construct novel nomograms for BrM risk prediction in NSCLC. Using Cox-proportional hazard models with L1-regularization, we predicted BrM risk at 6-month, 1-year, and 2-year follow-up intervals.</div></div><div><h3>Findings</h3><div>The patient cohort included 1904 patients (median age 68 years, range 38–94 years, BrM incidence 22.8%). The cohort included 1059 males (55.6%) and 845 females (44.4%). Of the cohort, 92.8% of patients identified as White (n = 1766), 1.0% as Asian (n = 19), 4.0% as Black (n = 77), and 2.2% as another race (n = 42). The Zhang 2021 model demonstrated the highest performance in predicting BrM incidence in our cohort, achieving an AUROC of 0.91 (95% CI: 0.87, 0.95). Two novel models were developed: a baseline model incorporating clinical and imaging data at diagnosis (cTNM stage, age at diagnosis), and an extended model including additional clinical and treatment data (number of extracranial metastatic sites, prior radiotherapy, chemotherapy, surgery, and histology) (<span><span>https://nmikolajewicz.shinyapps.io/nomogram_wilding2024/</span><svg><path></path></svg></span>). While both models showed similar short-term performance, the extended model demonstrated superior predictive capacity (AUROC 0.91 at 3-years) for longer-term outcomes. Our nomograms rely exclusively on clinical features routinely documented in patient records, thereby requiring no additional investigations.</div></div><div><h3>Interpretation</h3><div>These clinically accessible nomograms for BrM prediction will facilitate prognostic modeling, risk stratification, refinement of CNS screening guidelines, and patient counseling.</div></div><div><h3>Funding</h3><div>None.</div></div>\",\"PeriodicalId\":29783,\"journal\":{\"name\":\"Lancet Regional Health-Americas\",\"volume\":\"50 \",\"pages\":\"Article 101213\"},\"PeriodicalIF\":7.0000,\"publicationDate\":\"2025-08-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Lancet Regional Health-Americas\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2667193X25002236\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"HEALTH CARE SCIENCES & SERVICES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Lancet Regional Health-Americas","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2667193X25002236","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"HEALTH CARE SCIENCES & SERVICES","Score":null,"Total":0}
A nomogram to predict development of brain metastasis in non-small cell lung cancer patients: a retrospective analysis using routinely available medical records
Background
Brain metastases (BrM) are a frequent complication among patients with non-small cell lung cancer (NSCLC). While guidelines exist for baseline CNS screening in advanced NSCLC, surveillance strategies for early-stage disease remain limited. This study aimed to develop a time-dependent BrM risk prediction nomogram using readily available clinical information.
Methods
We analyzed a retrospective cohort of NSCLC patients at Penn State Health. Our objectives were to (1) systematically evaluate the performance of existing BrM risk prediction algorithms and (2) construct novel nomograms for BrM risk prediction in NSCLC. Using Cox-proportional hazard models with L1-regularization, we predicted BrM risk at 6-month, 1-year, and 2-year follow-up intervals.
Findings
The patient cohort included 1904 patients (median age 68 years, range 38–94 years, BrM incidence 22.8%). The cohort included 1059 males (55.6%) and 845 females (44.4%). Of the cohort, 92.8% of patients identified as White (n = 1766), 1.0% as Asian (n = 19), 4.0% as Black (n = 77), and 2.2% as another race (n = 42). The Zhang 2021 model demonstrated the highest performance in predicting BrM incidence in our cohort, achieving an AUROC of 0.91 (95% CI: 0.87, 0.95). Two novel models were developed: a baseline model incorporating clinical and imaging data at diagnosis (cTNM stage, age at diagnosis), and an extended model including additional clinical and treatment data (number of extracranial metastatic sites, prior radiotherapy, chemotherapy, surgery, and histology) (https://nmikolajewicz.shinyapps.io/nomogram_wilding2024/). While both models showed similar short-term performance, the extended model demonstrated superior predictive capacity (AUROC 0.91 at 3-years) for longer-term outcomes. Our nomograms rely exclusively on clinical features routinely documented in patient records, thereby requiring no additional investigations.
Interpretation
These clinically accessible nomograms for BrM prediction will facilitate prognostic modeling, risk stratification, refinement of CNS screening guidelines, and patient counseling.
期刊介绍:
The Lancet Regional Health – Americas, an open-access journal, contributes to The Lancet's global initiative by focusing on health-care quality and access in the Americas. It aims to advance clinical practice and health policy in the region, promoting better health outcomes. The journal publishes high-quality original research advocating change or shedding light on clinical practice and health policy. It welcomes submissions on various regional health topics, including infectious diseases, non-communicable diseases, child and adolescent health, maternal and reproductive health, emergency care, health policy, and health equity.