Kaylee Molin, Nathaniel Barry, Suki Gill, Ghulam Mubashar Hassan, Roslyn J Francis, Jeremy S L Ong, Martin A Ebert, Jake Kendrick
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Univariable analysis used Kaplan-Meier curves and Cox proportional hazards models to correlate individual features with overall survival. Multivariable analysis used the LASSO Cox proportional hazards method to create 13 models: radiomics-only, clinical-only, and various combinations of radiomic and clinical features. Each model included six features and was bootstrapped 1000 times to obtain concordance indices with 95% confidence intervals, followed by optimism correction. In the univariable analysis, 6 out of 8 clinical features and 68 out of 89 radiomic features were significantly correlated with overall survival, including age, disease stage, total lesional uptake and total lesional volume. The optimism-corrected concordance indices from the multivariable models were 0.722 (95% CI 0.653-0.784) for the clinical model, 0.681 (95% CI 0.616-0.745) for the radiomics model, and 0.704 (95% CI 0.648-0.768) for the combined model with three clinical and three radiomic features, when extracting radiomic features from the largest lesion only. While univariable analysis showed significant prognostic value for many radiomic features, their integration into multivariable models did not improve predictive accuracy beyond clinical features alone.</p>","PeriodicalId":48490,"journal":{"name":"Physical and Engineering Sciences in Medicine","volume":" ","pages":""},"PeriodicalIF":2.4000,"publicationDate":"2025-01-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Evaluating the prognostic value of radiomics and clinical features in metastatic prostate cancer using [<sup>68</sup>Ga]Ga-PSMA-11 PET/CT.\",\"authors\":\"Kaylee Molin, Nathaniel Barry, Suki Gill, Ghulam Mubashar Hassan, Roslyn J Francis, Jeremy S L Ong, Martin A Ebert, Jake Kendrick\",\"doi\":\"10.1007/s13246-024-01516-8\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Prostate cancer is a significant global health issue due to its high incidence and poor outcomes in metastatic disease. 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引用次数: 0
摘要
前列腺癌是一个重要的全球健康问题,由于其高发病率和预后差的转移性疾病。本研究旨在建立预测转移性生化复发性前列腺癌患者总体生存期的模型,潜在地帮助识别高风险患者并提供更有针对性的治疗方案。180例此类患者的多中心队列接受了[68Ga]Ga-PSMA-11 PET/CT扫描,病变半自动分割并从病变中提取放射学特征。分析分为单变量和多变量两个阶段。单变量分析使用Kaplan-Meier曲线和Cox比例风险模型将个体特征与总生存率联系起来。多变量分析使用LASSO Cox比例风险法创建13个模型:仅放射组学,仅临床,以及放射组学和临床特征的各种组合。每个模型包含6个特征,bootstrap 1000次,获得95%置信区间的一致性指数,然后进行乐观修正。在单变量分析中,8个临床特征中的6个和89个放射学特征中的68个与总生存率显著相关,包括年龄、疾病分期、病变总摄取和病变总体积。临床模型的乐观校正一致性指数为0.722 (95% CI 0.653-0.784),放射组学模型的乐观校正一致性指数为0.681 (95% CI 0.616-0.745),仅从最大病变提取放射组学特征时,具有三个临床和三个放射组学特征的联合模型的乐观校正一致性指数为0.704 (95% CI 0.648-0.768)。虽然单变量分析显示了许多放射学特征的显著预后价值,但将它们整合到多变量模型中并不能提高除临床特征之外的预测准确性。
Evaluating the prognostic value of radiomics and clinical features in metastatic prostate cancer using [68Ga]Ga-PSMA-11 PET/CT.
Prostate cancer is a significant global health issue due to its high incidence and poor outcomes in metastatic disease. This study aims to develop models predicting overall survival for patients with metastatic biochemically recurrent prostate cancer, potentially helping to identify high-risk patients and enabling more tailored treatment options. A multi-centre cohort of 180 such patients underwent [68Ga]Ga-PSMA-11 PET/CT scans, with lesions semi-automatically segmented and radiomic features extracted from lesions. The analysis included two phases: univariable and multivariable. Univariable analysis used Kaplan-Meier curves and Cox proportional hazards models to correlate individual features with overall survival. Multivariable analysis used the LASSO Cox proportional hazards method to create 13 models: radiomics-only, clinical-only, and various combinations of radiomic and clinical features. Each model included six features and was bootstrapped 1000 times to obtain concordance indices with 95% confidence intervals, followed by optimism correction. In the univariable analysis, 6 out of 8 clinical features and 68 out of 89 radiomic features were significantly correlated with overall survival, including age, disease stage, total lesional uptake and total lesional volume. The optimism-corrected concordance indices from the multivariable models were 0.722 (95% CI 0.653-0.784) for the clinical model, 0.681 (95% CI 0.616-0.745) for the radiomics model, and 0.704 (95% CI 0.648-0.768) for the combined model with three clinical and three radiomic features, when extracting radiomic features from the largest lesion only. While univariable analysis showed significant prognostic value for many radiomic features, their integration into multivariable models did not improve predictive accuracy beyond clinical features alone.