Your browser doesn't support javascript.
loading
Diagnostic value of bone metabolic markers for bone metastasis of non-small cell lung cancer analyzed by Logistic regression combined with ROC curve / 肿瘤研究与临床
Cancer Research and Clinic ; (6): 162-164,173, 2016.
Article em Zh | WPRIM | ID: wpr-603710
Biblioteca responsável: WPRO
ABSTRACT
Objective To investigate the diagnostic value of bone metabolic markers (BGP, β-CTX and PINP) for bone metastasis of non-small cell lung cancer (NSCLC) analyzed by Logistic regression combined with ROC curve.Methods A total of 65 patients with stage Ⅳ NSCLC were enrolled in this study.The patients were divided into two groups based on radiological imaging, includirg bone metastasis group (30 cases) and non-bone metastasis group (35 cases).The serum concentrations of BGP, β-CTX and PINP were measured by electrochemical method.Logistic regression and ROC curve were applied to analyze the data and evaluate the diagnostic values.Results The concentrations of β-CTX [(0.54±0.39) ng/ml] and PINP [(103.64±81.86) ng/ml] were significantly higher in bone metastasis group than those [(0.31±0.16) ng/ml and (48.37±27.76) ng/ml, respectively] in non-bone metastasis group (P < 0.01), while the level of BGP did not differ between two groups (P > 0.05).The area under the ROC curve (AUC) for β-CTX and PINP was 0.662 and 0.678, respectively.The AUC for the new predictive variables created by Logistic regression was 0.761.Conclusion Combined detection of β-CTX and PINP in the serum and application of Logistic regression combined with ROC curve analysis can increase diagnostic accuracy on bone metastasis of NSCLC.
Palavras-chave
Texto completo: 1 Índice: WPRIM Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Idioma: Zh Revista: Cancer Research and Clinic Ano de publicação: 2016 Tipo de documento: Article
Texto completo: 1 Índice: WPRIM Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Idioma: Zh Revista: Cancer Research and Clinic Ano de publicação: 2016 Tipo de documento: Article