Is pre-therapeutical FDG-PET/CT capable to detect high risk tumor subvolumes responsible for local failure in non-small cell lung cancer?

被引:86
作者
Abramyuk, Andrij [1 ]
Tokalov, Sergey
Zoephel, Klaus [2 ]
Koch, Arne
Lazanyi, Kornelia Szluha
Gillham, Charles [3 ]
Herrmann, Thomas [4 ]
Abolmaali, Nasreddin
机构
[1] Tech Univ Dresden, OncoRay Ctr Radiat Res Oncol, Med Fac Carl Gustav Carus Biol & Mol Imaging, D-01307 Dresden, Germany
[2] Tech Univ Dresden, Clin & Policlin Nucl Med, D-01307 Dresden, Germany
[3] Acad Unit Clin & Mol Oncol, Dublin, Ireland
[4] Tech Univ Dresden, Clin & Policlin Radiotherapy & Radiat Oncol, D-01307 Dresden, Germany
关键词
FDG-PET/CT; Radiotherapy planning; Non-small-cell lung cancer; POSITRON-EMISSION-TOMOGRAPHY; 3-DIMENSIONAL CONFORMAL RADIOTHERAPY; MODULATED RADIATION-THERAPY; TARGET VOLUME DEFINITION; INTEROBSERVER VARIABILITY; THORACIC RADIOTHERAPY; DELINEATION; CT; INCREASE; PATTERNS;
D O I
10.1016/j.radonc.2009.01.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background and purpose: Local failure is a significant issue following radiotherapy (RT) for patients with non-small cell lung cancer (NSCLC). The aim of this study was to find out whether FDG-PET/CT is capable to predict tumor relapse location in patients with NSCLC, ill Particular to determine high risk tumors' subvolumes responsible for local failure. Material and methods: Ten patients with locoregional relapse of NSCLC underwent FDG-PET/CT before, during, and in the 4-12 months following curative chemoradiotherapy (ChRT, 66 Gy) using a combined PET/CT scanner. Morphologic and metabolic tumor volumetry and an evaluation of FDG-uptake dynamics were performed. Results: CT showed partial reduction of tumor Volume after RT in all patients. PET-revealed partial in eight patients and complete metabolic response in two patients during RT. Six to nine months after RT, local failure was diagnosed in all patients with both methods. Tumor recurrences were localized mostly in the most active ones of pre-therapeutically metabolic regions of the primary tumor. Conclusions: Local failure in NSCLC appears most common at the primary site and within the irradiated target Volume with the highest FDG uptake. This observation may be useful for further optimization of radiotherapy of NSCLC, for example, by the application of additional radiation dose to subvolumes of primary tumors with higher FDG uptake. (C) 2009 Elsevier Ireland Ltd. All rights reserved. Radiotherapy and Oncology 91 (2009) 399-404
引用
收藏
页码:399 / 404
页数:6
相关论文
共 37 条
[1]   The contribution of integrated PET/CT to the evolving definition of treatment volumes in radiation treatment planning in lung cancer [J].
Ashamalla, H ;
Rafla, S ;
Parikh, K ;
Mokhtar, B ;
Goswami, G ;
Kambam, S ;
Abdel-Dayem, H ;
Guirguis, A ;
Ross, P ;
Evola, A .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2005, 63 (04) :1016-1023
[2]   Theragnostic imaging for radiation oncology: dose-painting by numbers [J].
Bentzen, SM .
LANCET ONCOLOGY, 2005, 6 (02) :112-117
[3]   Defining a radiotherapy target with positron emission tomography [J].
Black, QC ;
Grills, IS ;
Kestin, LL ;
Wong, CYO ;
Wong, JW ;
Martinez, AA ;
Yan, D .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2004, 60 (04) :1272-1282
[4]  
Burgman P, 2001, J NUCL MED, V42, P170
[5]   Observer variation in contouring gross tumor volume in patients with poorly defined non-small-cell lung tumors on CT:: The impact of 18FDG-hybrid PET fusion [J].
Caldwell, CB ;
Mah, K ;
Ung, YC ;
Danjoux, CE ;
Balogh, JM ;
Ganguli, SN ;
Ehrlich, LE .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2001, 51 (04) :923-931
[6]   A novel approach to overcome hypoxic tumor resistance: Cu-ATSM-guided intensity-modulated radiation therapy [J].
Chao, KSC ;
Bosch, WR ;
Mutic, S ;
Lewis, JS ;
Dehdashti, F ;
Mintun, MA ;
Dempsey, JF ;
Perez, CA ;
Purdy, JA ;
Welch, MJ .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2001, 49 (04) :1171-1182
[7]   Molecular (functional) imaging for radiotherapy applications: An RTOG symposium [J].
Chapman, JD ;
Bradley, JD ;
Eary, JF ;
Haubner, R ;
Larson, SM ;
Michalski, JM ;
Okunieff, PG ;
Strauss, HW ;
Ung, YC ;
Welch, MJ .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2003, 55 (02) :294-301
[8]   Phase II multicenter study of induction chemotherapy followed by concurrent efaproxiral (RSR13) and thoracic radiotherapy for patients with locally advanced non-small-cell lung cancer [J].
Choy, H ;
Nabid, A ;
Stea, B ;
Scott, C ;
Roa, W ;
Kleinberg, L ;
Ayoub, J ;
Smith, C ;
Souhami, L ;
Hamburg, S ;
Spanos, W ;
Kreisman, H ;
Boyd, AP ;
Cagnoni, PJ ;
Curran, WJ .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (25) :5918-5928
[9]   Comparison of inverse-planned three-dimensional conformal radiotherapy and intensity-modulated radiotherapy for non-small-cell lung cancer [J].
Christian, Judith A. ;
Bedford, James L. ;
Webb, Steve ;
Brada, Michael .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2007, 67 (03) :735-741
[10]  
Daisne JF, 2006, B CANCER, V93, P1175