Whole body metabolic tumor volume is a prognostic marker in patients with newly diagnosed stage 3B non-small cell lung cancer, confirmed with external validation

Abstract Purpose TNM Stage 3B encompasses a wide range of primary tumor and nodal metastatic tumor burden. This study aimed to evaluate the prognostic value of quantitative FDG PET/CT parameters in patients with newly diagnosed Stage 3B Non-Small Cell Lung Cancer (NSCLC). Materials and Methods Insti...

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Main Authors: Brittany Z. Dashevsky, Chenpeng Zhang, Li Yan, Cindy Yuan, Lingyun Xiong, Yongmei Liu, Haiyan Liu, Feng-Ming Spring Kong, Yonglin Pu
Format: Article
Language:English
Published: SpringerOpen 2017-12-01
Series:European Journal of Hybrid Imaging
Subjects:
Online Access:http://link.springer.com/article/10.1186/s41824-017-0013-z
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author Brittany Z. Dashevsky
Chenpeng Zhang
Li Yan
Cindy Yuan
Lingyun Xiong
Yongmei Liu
Haiyan Liu
Feng-Ming Spring Kong
Yonglin Pu
author_facet Brittany Z. Dashevsky
Chenpeng Zhang
Li Yan
Cindy Yuan
Lingyun Xiong
Yongmei Liu
Haiyan Liu
Feng-Ming Spring Kong
Yonglin Pu
author_sort Brittany Z. Dashevsky
collection DOAJ
description Abstract Purpose TNM Stage 3B encompasses a wide range of primary tumor and nodal metastatic tumor burden. This study aimed to evaluate the prognostic value of quantitative FDG PET/CT parameters in patients with newly diagnosed Stage 3B Non-Small Cell Lung Cancer (NSCLC). Materials and Methods Institutional review board approved retrospective study identified patients diagnosed with Stage 3B NSCLC (8th edition TNM classification) on baseline FDG PET/CT at two medical centers (Medical centers A and B), between Feb 2004 and Dec 2014. Patients were excluded if they had prior NSCLC treatment or recent diagnosis of a second primary cancer. Quantitative FDG PET/CT parameters including whole body metabolic tumor volume (MTVwb), total lesion glycolysis (TLGwb), and maximum standardized uptake value (SUVmaxwb) were measured from baseline PET/CT using Edge method with Mimvista software. The primary endpoint was overall survival (OS). Cox proportional hazard regression and Kaplan-Meier overall survival analyses were used to test for an association between OS and quantitative FDG PET/CT parameters. The distributions of MTVwb, TLGwb, SUVmaxwb were skewed, so a natural logarithm transformation was applied and the transformed variables [(ln(MTVwb), ln(TLGwb), and ln(SUVmaxwb)] were used in the analysis. Results The training set included 110 patients from center A with Stage 3B NSCLC. 78.2% of patients expired during follow-up. Median OS was 14 months. 1-year, 2-year, and 5-year OS was 56.5%, 34.6% and 13.9%, respectively. Univariate Cox regression analysis showed no significant difference in OS on the basis of age, gender, histology, ln(TLGwb), or ln(SUVmaxwb). ln(MTVwb) was positively associated with OS [hazard ratio (HR) of 1.23, p = 0.037]. This association persisted on multivariate Cox regression analysis (HR 1.28, p = 0.043), with adjustments for age, gender, treatment and tumor histology. External validation with 44 patients from center B confirmed increasing MTVwb was associated significantly worse OS. An MTVwb cut-off point of 85.6 mL significantly stratified Stage 3B NSCLC patient prognosis. Conclusion MTVwb is a prognostic marker for OS in patients with Stage 3B NSCLC, independent of age, gender, treatment, and tumor histology.
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spelling doaj.art-4ec4906916044ee58fd2ffab13f428e72022-12-22T00:52:14ZengSpringerOpenEuropean Journal of Hybrid Imaging2510-36362017-12-011111010.1186/s41824-017-0013-zWhole body metabolic tumor volume is a prognostic marker in patients with newly diagnosed stage 3B non-small cell lung cancer, confirmed with external validationBrittany Z. Dashevsky0Chenpeng Zhang1Li Yan2Cindy Yuan3Lingyun Xiong4Yongmei Liu5Haiyan Liu6Feng-Ming Spring Kong7Yonglin Pu8Department of Radiology, University Of ChicagoDepartment of Nuclear Medicine, RenJi Hospital, School of Medicine, Shanghai Jiao Tong UniversityDepartment of Radiation Oncology, Linyi People’s HospitalDepartment of Radiology, University Of ChicagoDepartment of Radiology, University Of ChicagoDepartment of Thoracic Oncology, China West University HospitalDepartment of Nuclear Medicine, First Hospital of Shanxi Medical University and Molecular Imaging Precision Medical Collaborative Innovation Center, Shanxi Medical UniversityRadiation Oncology, Medical and Molecular Genetics, Indiana University School of MedicineDepartment of Radiology, University Of ChicagoAbstract Purpose TNM Stage 3B encompasses a wide range of primary tumor and nodal metastatic tumor burden. This study aimed to evaluate the prognostic value of quantitative FDG PET/CT parameters in patients with newly diagnosed Stage 3B Non-Small Cell Lung Cancer (NSCLC). Materials and Methods Institutional review board approved retrospective study identified patients diagnosed with Stage 3B NSCLC (8th edition TNM classification) on baseline FDG PET/CT at two medical centers (Medical centers A and B), between Feb 2004 and Dec 2014. Patients were excluded if they had prior NSCLC treatment or recent diagnosis of a second primary cancer. Quantitative FDG PET/CT parameters including whole body metabolic tumor volume (MTVwb), total lesion glycolysis (TLGwb), and maximum standardized uptake value (SUVmaxwb) were measured from baseline PET/CT using Edge method with Mimvista software. The primary endpoint was overall survival (OS). Cox proportional hazard regression and Kaplan-Meier overall survival analyses were used to test for an association between OS and quantitative FDG PET/CT parameters. The distributions of MTVwb, TLGwb, SUVmaxwb were skewed, so a natural logarithm transformation was applied and the transformed variables [(ln(MTVwb), ln(TLGwb), and ln(SUVmaxwb)] were used in the analysis. Results The training set included 110 patients from center A with Stage 3B NSCLC. 78.2% of patients expired during follow-up. Median OS was 14 months. 1-year, 2-year, and 5-year OS was 56.5%, 34.6% and 13.9%, respectively. Univariate Cox regression analysis showed no significant difference in OS on the basis of age, gender, histology, ln(TLGwb), or ln(SUVmaxwb). ln(MTVwb) was positively associated with OS [hazard ratio (HR) of 1.23, p = 0.037]. This association persisted on multivariate Cox regression analysis (HR 1.28, p = 0.043), with adjustments for age, gender, treatment and tumor histology. External validation with 44 patients from center B confirmed increasing MTVwb was associated significantly worse OS. An MTVwb cut-off point of 85.6 mL significantly stratified Stage 3B NSCLC patient prognosis. Conclusion MTVwb is a prognostic marker for OS in patients with Stage 3B NSCLC, independent of age, gender, treatment, and tumor histology.http://link.springer.com/article/10.1186/s41824-017-0013-zLung cancerTumor volumeFDG, PET/CT
spellingShingle Brittany Z. Dashevsky
Chenpeng Zhang
Li Yan
Cindy Yuan
Lingyun Xiong
Yongmei Liu
Haiyan Liu
Feng-Ming Spring Kong
Yonglin Pu
Whole body metabolic tumor volume is a prognostic marker in patients with newly diagnosed stage 3B non-small cell lung cancer, confirmed with external validation
European Journal of Hybrid Imaging
Lung cancer
Tumor volume
FDG, PET/CT
title Whole body metabolic tumor volume is a prognostic marker in patients with newly diagnosed stage 3B non-small cell lung cancer, confirmed with external validation
title_full Whole body metabolic tumor volume is a prognostic marker in patients with newly diagnosed stage 3B non-small cell lung cancer, confirmed with external validation
title_fullStr Whole body metabolic tumor volume is a prognostic marker in patients with newly diagnosed stage 3B non-small cell lung cancer, confirmed with external validation
title_full_unstemmed Whole body metabolic tumor volume is a prognostic marker in patients with newly diagnosed stage 3B non-small cell lung cancer, confirmed with external validation
title_short Whole body metabolic tumor volume is a prognostic marker in patients with newly diagnosed stage 3B non-small cell lung cancer, confirmed with external validation
title_sort whole body metabolic tumor volume is a prognostic marker in patients with newly diagnosed stage 3b non small cell lung cancer confirmed with external validation
topic Lung cancer
Tumor volume
FDG, PET/CT
url http://link.springer.com/article/10.1186/s41824-017-0013-z
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