Volume 62, Issue 1 pp. 81-90
Medical Imaging—Radiation Oncology—Original Article

Impact of tumour motion compensation and delineation methods on FDG PET-based dose painting plan quality for NSCLC radiation therapy

Hannah Mary Thomas

Hannah Mary Thomas

Department of Radiation Oncology, School of Medicine, University of Washington, Seattle, Washington, USA

Department of Physics, School of Advanced Sciences, VIT University, Vellore, India

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Paul E Kinahan

Paul E Kinahan

Department of Radiology, School of Medicine, University of Washington, Seattle, Washington, USA

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James Jebaseelan E Samuel

James Jebaseelan E Samuel

Department of Physics, School of Advanced Sciences, VIT University, Vellore, India

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Stephen R Bowen

Corresponding Author

Stephen R Bowen

Department of Radiation Oncology, School of Medicine, University of Washington, Seattle, Washington, USA

Department of Radiology, School of Medicine, University of Washington, Seattle, Washington, USA

Correspondence

Dr Stephen R Bowen, Departments of Radiology and Radiation Oncology, University of Washington School of Medicine, 1959 NE Pacific St. Box 356043, Seattle, WA 98195, USA

Email: [email protected]

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First published: 28 November 2017
Citations: 11
HM Thomas PhD; PE Kinahan PhD; JJE Samuel PhD; SR Bowen PhD.
Conflict of interest: None.

Abstract

Introduction

To quantitatively estimate the impact of different methods for both boost volume delineation and respiratory motion compensation of [18F] FDG PET/CT images on the fidelity of planned non-uniform ‘dose painting’ plans to the prescribed boost dose distribution.

Methods

Six locally advanced non-small cell lung cancer (NSCLC) patients were retrospectively reviewed. To assess the impact of respiratory motion, time-averaged (3D AVG), respiratory phase-gated (4D GATED) and motion-encompassing (4D MIP) PET images were used. The boost volumes were defined using manual contour (MANUAL), fixed threshold (FIXED) and gradient search algorithm (GRADIENT). The dose painting prescription of 60 Gy base dose to the planning target volume and an integral dose of 14 Gy (total 74 Gy) was discretized into seven treatment planning substructures and linearly redistributed according to the relative SUV at every voxel in the boost volume. Fifty-four dose painting plan combinations were generated and conformity was evaluated using quality index VQ0.95–1.05, which represents the sum of planned dose voxels within 5% deviation from the prescribed dose. Trends in plan quality and magnitude of achievable dose escalation were recorded.

Results

Different segmentation techniques produced statistically significant variations in maximum planned dose (P < 0.02), as well as plan quality between segmentation methods for 4D GATED and 4D MIP PET images (P < 0.05). No statistically significant differences in plan quality and maximum dose were observed between motion-compensated PET-based plans (P > 0.75). Low variability in plan quality was observed for FIXED threshold plans, while MANUAL and GRADIENT plans achieved higher dose with lower plan quality indices.

Conclusions

The dose painting plans were more sensitive to segmentation of boost volumes than PET motion compensation in this study sample. Careful consideration of boost target delineation and motion compensation strategies should guide the design of NSCLC dose painting trials.

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