Positron emission tomography for target volume definition in the treatment of non-small cell lung cancer

被引:47
作者
Lavrenkov, K
Partridge, M
Cook, G
Brada, M
机构
[1] Royal Marsden NHS Fdn Trust, Lung Res Unit, Sutton SM2 5PT, Surrey, England
[2] Royal Marsden NHS Fdn Trust, Joint Dept Phys, Sutton SM2 5PT, Surrey, England
[3] Royal Marsden NHS Fdn Trust, Dept Nucl Med & PET, Sutton SM2 5PT, Surrey, England
[4] Inst Canc Res, Acad Unit Radiotherapy & Oncol, Surrey, England
关键词
non-small cell lung cancer; radiotherapy treatment planning; positron emission tomography; computerised tomography;
D O I
10.1016/j.radonc.2005.09.016
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The additional benefit of positron emission tomography (PET) in the initial staging of non-small cell lung cancer (NSCLC) has generated interest in F-18-fluorodeoxyglucose (FDG) PET as a means of defining the extent of primary lung tumour for radiotherapy treatment planning (RTP). A review of published data suggests that PET results in a reduction in the CT-derived GTV for NSCLC primary target volume in 15% of the patients. This is principally due to the ability of PET to distinguish tumour from atelectasis. However, the difficulty of tumour edge definition, limited spatial resolution and tumour motion during image acquisition currently limits the accuracy of PET in target volume delineation in NSCLC without adjacent lung consolidation. This is compounded by the lack of data correlating PET with spatial pathology at the primary tumour site. With the current technical limitations, it is not established that PET can add accuracy to the CT-defined primary target delineation in RTP of NSCLC. It is hoped that advances in PET and combined PET/CT imaging may overcome some of the technical limitations. Future use of PET for primary tumour delineation in NSCLC will also be critically dependent on the detailed studies of imaging-pathology correlation. (C) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
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页码:1 / 4
页数:4
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