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Primary tumor PET/CT [(18)F]FDG uptake is an independent predictive factor for regional lymph node metastasis in patients with non-small cell lung cancer

Aim: To investigate the correlation between [(18)F]fluorodeoxyglucose (FDG) uptake in a primary tumor and pathologic N stages, and to further analyze the possible risk factors contributing to the regional lymph node metastasis. Patients and methods: Eighty patients with non-small cell lung cancer (N...

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Detalles Bibliográficos
Autores principales: Li, Meng, Wu, Ning, Zheng, Rong, Liang, Ying, Liu, Ying, Zhang, Wenjie, Li, Ni, Zhao, Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: e-Med 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569669/
https://www.ncbi.nlm.nih.gov/pubmed/23399986
http://dx.doi.org/10.1102/1470-7330.2012.0040
Descripción
Sumario:Aim: To investigate the correlation between [(18)F]fluorodeoxyglucose (FDG) uptake in a primary tumor and pathologic N stages, and to further analyze the possible risk factors contributing to the regional lymph node metastasis. Patients and methods: Eighty patients with non-small cell lung cancer (NSCLC) who underwent positron emission tomography/computed tomography were enrolled in the study. The FDG uptake in the primary tumor was compared for the different N staging groups and further correlation was performed. The degree of FDG uptake in the primary tumor and other possible variables related to the incidence of lymph node metastasis were examined by univariate and logistic multivariate analysis. FDG uptake was quantitated using the maximum standardized uptake value (SUV(max)). Results: Statistically significant differences were found in the SUV(max) of the primary tumors among different N staging groups (F = 4.124, P = 0.023), and the correlation between them was also statistically significant (r = 0.438, P = 0.000). Univariate analysis showed that blood tumor markers, primary tumor size, histologic grade, and SUV(max) of the primary tumor were significantly associated with lymph node involvement. Logistic multivariate analysis showed that blood tumor makers and SUV(max) of primary tumor might be considered as significant predictive factors for lymph node metastasis in patients with NSCLC. Conclusion: Our results show that there is a significant relationship between the SUV(max) of the primary tumor and the pathologic N stage of NSCLC. FDG uptake by the primary tumor may be an independent predictor of regional lymph node metastasis in patients with NSCLC.