Abstract

Respiration‐induced tumor motion during intensity‐modulated radiotherapy (IMRT) of non‐small‐cell lung cancer (NSCLC) could cause substantial differences between planned and delivered doses. While it has been shown that, for conventionally fractionated IMRT, motion effects average out over the course of many treatments, this might not be true for hypofractionated IMRT (IMHFRT). Numerical simulations were performed for nine NSCLC patients (11 tumors) to evaluate this problem. Dose distributions to the Clinical Target Volume (CTV) and Internal Target Volume (ITV) were retrospectively calculated using the previously‐calculated leaf motion files but with the addition of typical periodic motion (i.e. amplitude 0.36–1.26 cm, 3–8 sec period). A typical IMHFRT prescription of 20 Gy × 3 fractions was assumed. For the largest amplitude (1.26 cm), the average ± standard deviation of the ratio of simulated to planned mean dose, minimum dose, D95 and V95 were 0.98±0.01, 0.88±0.09, 0.94±0.05 and 0.94±0.07 for the CTV, and 0.99±0.01, 0.99±0.03, 0.98±0.02 and 1.00±0.01 for the ITV, respectively. There was minimal dependence on period or initial phase. For typical tumor geometries and respiratory amplitudes, changes in target coverage are minimal but can be significant for larger amplitudes, faster beam delivery, more highly‐modulated fields, and smaller field margins.PACS number: 87.55.dk

Highlights

  • Conformal photon dose distributions generated with intensity-modulated radiation therapy (IMRT) often improve the therapeutic ratio, permitting higher tumor doses while respecting normal tissue tolerance

  • The non-small-cell lung cancer (NSCLC) IMHFRT treatments typically require relatively modest beam modulation, but we examined the effect of respiratory motion on treatment plans with more highlymodulated beams

  • Similar motion effects were seen for parallel leaf and tumor motions

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Summary

Introduction

Conformal photon dose distributions generated with intensity-modulated radiation therapy (IMRT) often improve the therapeutic ratio, permitting higher tumor doses while respecting normal tissue tolerance. Blurring[11,12,13,14,15,16,17] refers to changes in dose to a target voxel caused by motion to a region, where the dose is very different from what was planned. It is dependent on respiration amplitude and the degree of modulation in the plan. IMRT interplay refers to a change in delivered dose caused by tumor motion relative to MLC leaf motion. The expectation value of a patient’s dose distribution is a function mostly of blurring, while statistical variation is mostly determined by interplay

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