Non Small Cell Lung Cancer Clinical Trial
Official title:
DE-CT vs. SE-CT as Optimal Imaging During Treatment for Adaptive Proton Therapy in Stage III Non Small Cell Lung Cancer (NSCLC)
Dose distribution calculations for proton therapy are more accurate when based on DE-CT than on SE-CT. It is however unclear what the quantitative benefit of repeated DE-CT calculations is for lung cancer patients.
In order to calculate the dose distribution of protons adequately, accurate estimations of
the stopping power ratio (SPR) medium to water, are required. Using a conversion from single
energy CT (SE-CT) images results in an uncertainty in the SPR of at least 3-4%. This
uncertainty results in in the use of larger margins around the clinical target volume (CTV)
and hence more dose to the organs at risk (OAR). It also effects in the conservative use of
beam directions, which are often sub-optimal, to avoid irradiating normal tissues.
Dual energy CT (DE-CT) improves the accuracy of the SPR and therefore the proton range
estimation.
An evaluation of the proton range for several tissues using SE-CT and DE-CT as input to
Monte Carlo (MC) simulations showed on average improvements in range prediction from 0.1% to
2.1% when using DECT instead of SECT, but in several phantoms and also versus proton-CT, the
errors on SE-CT based proton stopping power ratios are reported to be more than 7 %.
A limitation of these studies is that most of them were performed in phantoms. In the first
clinical data set on five patients with base of skull tumours, it was reported that although
the SPR estimation was indeed better for DE-CT than for SE-CT, its clinical relevance was
unclear. However, in the same study, phantom measurements showed a large uncertainty of the
SPR in the lung. This is due to the large heterogeneity of the lungs and the huge difference
in the density of the lungs compared to the mediastinum, the tumour and the chest cavity.
It is therefore important to study the SPR differences of SE-CT compared to DE-CT in lung
cancer patients and the impact on the dose distribution especially in the context of
adaptive radiotherapy. As during the course of concurrent chemotherapy and radiotherapy,
which is the standard treatment in the majority of stage III lung cancer patients, important
anatomical changes may occur, it is also of clinical relevance to determine the influence of
repeated dose calculations on DE-CT.
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