Evaluation of a target contouring protocol for 3D conformal radiotherapy in non-small cell lung cancer

Citation
S. Senan et al., Evaluation of a target contouring protocol for 3D conformal radiotherapy in non-small cell lung cancer, RADIOTH ONC, 53(3), 1999, pp. 247-255
Citations number
26
Categorie Soggetti
Radiology ,Nuclear Medicine & Imaging","Onconogenesis & Cancer Research
Journal title
RADIOTHERAPY AND ONCOLOGY
ISSN journal
01678140 → ACNP
Volume
53
Issue
3
Year of publication
1999
Pages
247 - 255
Database
ISI
SICI code
0167-8140(199912)53:3<247:EOATCP>2.0.ZU;2-M
Abstract
Background: A protocol for the contouring of target volumes in lung cancer was implemented. Subsequently, a study was performed in order to determine the intra and inter-clinician variations in contoured volumes. Materials and methods: Six radiation oncologists (RO) contoured the gross t umour volume (GTV) and/or clinical target volume (CTV), and planning target volume (PTV) for three patients with non-small cell lung cancer (NSCLC), o n two separate occasions. These were, respectively, a well-circumscribed T1 N0M0 lesion, an irregularly shaped T2N0M0 lesion, and a T2N2M0 tumour. Deta iled diagnostic radiology reports were provided and contours were entered i nto a 3D planning system. The target volumes were calculated and beams-eye view (BEV) plots were generated to visualise differences in contouring. A s oftware tool was used to expand the GTV and CTV in three dimensions for an automatically derived PTV. Results: Significant inter-RO variations in contoured target volumes were o bserved for all patients, and these were greater than intra-RO differences. The ratio of the largest to smallest contoured volume ranged from 1.6 for the GTV in the T1N0 lesion, to 2.0 for the PTV in the T2N2 lesion. The BEV plots revealed significant inter-RO variations in contouring the mediastina l CTV. The PTV's derived using a 3D margin programme were larger than manua lly contoured PTV's. These variations did not correlate with the experience of ROs. Conclusions: Despite the use of an institutional contouring protocol, signi ficant interclinician variations persist in contouring target volumes in NS CLC. Additional measures to decrease such variations should be incorporated into clinical trials. (C) 1999 Elsevier Science Ireland Ltd. All rights re served.