Identification of residual metabolic-active areas within individual NSCLC tumours using a pre-radiotherapy 18Fluorodeoxyglucose-PET-CT scan

被引:180
作者
Aerts, Hugo J. W. L. [1 ]
van Baardwijk, Angela A. W. [1 ]
Petit, Steven F. [1 ]
Offermann, Claudia [1 ]
van Loon, Judith [1 ]
Houben, Ruud [1 ]
Dingemans, Anne-Marie C. [2 ]
Wanders, Rinus [1 ]
Boersma, Liesbeth [1 ]
Borger, Jacques [1 ]
Bootsma, Gerben [3 ]
Geraedts, Wiel [4 ]
Pitz, Cordula [5 ]
Simons, Jean [6 ]
Wouters, Bradly G. [1 ]
Oellers, Michel [1 ]
Lambin, Philippe [1 ]
Bosmans, Geert [1 ]
Dekker, Andre L. A. J. [1 ]
De Ruysscher, Dirk [1 ]
机构
[1] Univ Maastricht, Dept Radiat Oncol MAASTRO, Grow Sch Oncol & Dev Biol, NL-6229 ET Maastricht, Netherlands
[2] Univ Maastricht, Med Ctr, Dept Lung Dis, NL-6229 ET Maastricht, Netherlands
[3] Atrium Med Ctr, Heerlen, Netherlands
[4] Maasland Hosp, Sittard, Netherlands
[5] Laurentius Hosp, Roermond, Netherlands
[6] Sint Jans Gasthuis, Weert, Netherlands
关键词
Intra-tumour heterogeneity; Residual metabolic activity; Radio-resistance; Non-small cell lung cancer; PET-CT; CELL LUNG-CANCER; POSITRON-EMISSION-TOMOGRAPHY; STANDARDIZED UPTAKE VALUE; RADIATION-THERAPY; DOSE-ESCALATION; PHASE-II; SEQUENTIAL CHEMORADIOTHERAPY; ACCELERATED RADIOTHERAPY; INDUCTION CHEMOTHERAPY; FDG UPTAKE;
D O I
10.1016/j.radonc.2009.03.006
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Background and purpose: Non-small cell lung cancer (NSCLC) tumours are mostly heterogeneous. We hypothesized that areas within the turnout with a high pre-radiation F-18-deoxyglucose (FDG) uptake, could identify residual metabolic-active areas, ultimately enabling selective-boosting of turnout sub-volumes. Material and methods: Fifty-five patients with inoperable stage I-III NSCLC treated with chemo-radiation or with radiotherapy alone were included. For each patient one pre-radiotherapy and one post-radiotherapy FDG-PET-CT scans were available. Twenty-two patients showing persistent FDG uptake in the primary turnout after radiotherapy were analyzed. Overlap fractions (OFs) were calculated between standardized uptake value (SUV) threshold-based auto-delineations on the pre- and post-radiotherapy scan. Results: Patients with residual metabolic-active areas within the tumour had a significantly worse survival compared to individuals with a complete metabolic response (p = 0.002). The residual metabolicactive areas within the tumour largely corresponded (OF > 70%) with the 50%SUV high FDG uptake area of the pre-radiotherapy scan. The hotspot within the residual area (90%SUV) was completely within the GTV (OF = 100%), and had a high overlap with the pre-radiotherapy 50%SUV threshold (OF > 84%). Conclusions: The location of residual metabolic-active areas within the primary tumour after therapy corresponded with the original high FDG uptake areas pre-radiotherapy. Therefore, a single pre-treatment FDG-PET-CT scan allows for the identification of residual metabolic-active areas. (C) 2009 Elsevier Ireland Ltd. All rights reserved. Radiotherapy and Oncology 91 (2009) 386-392
引用
收藏
页码:386 / 392
页数:7
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