An alternative parameter for early forecasting clinical response in NSCLC patients during radiotherapy: proof of concept study

被引:2
|
作者
Padovani, Laetitia [1 ,2 ]
Baret, Aurelie [2 ]
Ciccolini, Joseph [1 ]
Taieb, David [3 ]
Bardia, Farman [3 ]
Teissonnier, Laetitia [3 ]
Muracciole, Xavier [1 ,2 ]
Barlesi, Fabrice [1 ,4 ]
Barbolosi, Dominique [1 ]
机构
[1] Aix Marseille Univ, SMARTc, INSERM, UMR CRO2 911, Marseille, France
[2] Assistance Publ Hop Marseille, Dept Radiotherapy, Marseille, France
[3] Aix Marseille Univ, Assistance Publ Hop Marseille, Dept Nucl Med, Marseille, France
[4] Aix Marseille Univ, Assistance Publ Hop Marseille, Multidisciplinary Oncol & Therapeut Innovat Dept, Marseille, France
来源
BRITISH JOURNAL OF RADIOLOGY | 2016年 / 89卷 / 1062期
关键词
POSITRON-EMISSION-TOMOGRAPHY; CELL LUNG-CANCER; F-18-FDG PET; SURVIVAL; RADIOCHEMOTHERAPY; THERAPY; INDEX;
D O I
10.1259/bjr.20160061
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Objective: Positron emission tomography with F-18 fludeoxyglucose integrated with CT (F-18-FDG PET/CT) is a recommended imaging procedure in the evaluation of non-small-cell lung cancers (NSCLCs). Radiochemotherapy (RCT) is a mainstay for treatment of locally advanced NSCLC, for which overall survival still remains poor. Early evaluation of treatment response may help in decision-making to complete radiotherapy (RT) or to switch to other treatment modalities. The present study aimed to evaluate the performance of new metabolic parameters based on a simplified kinetic analysis on a single time point (SKA-S)-derived mathematical method, as compared with standardized uptake value (SUV) measurement during RT. Methods: Four patients treated with RT or RCT for NSCLC were evaluated using F-18-FDG PET/CT during RT and after treatment completion. Whole-body F-18-FDG PET/CT was performed followed by four additional list-mode acquisitions centered over the target lesion. Response was evaluated at four times (i.e. PET1-PET4) by calculating standard SUV values and T80%, the time taken to reach 80% of F-18-FDG metabolized fraction using a SKA-S-derived mathematical method. Results: Data from SUV and T80% calculations were found to be controversial. T80% was found to be more predictive of clinical outcome. Conclusion: Although results from this pilot study should be further confirmed in a large prospective study, the data suggest that T80% is a promising metabolic biomarker for assessing early response to RT. Advances in knowledge: In this proof of concept study, we show that T80% defined from a mathematic model taking into account the net influx rate constant and vascular volume could be consider as a promising biomarker as compared with the maximum SUV.
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页数:4
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