Summarising
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Models to convert dose distributions into clinical outcome
exist and have been verified in certain cases (e.g. rectum,
lung, liver)
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Care must taken if extending the application outside the
range where the parameter-fitting has been done
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If possible, take into account the weight of the clinical
variables (including the genetic ones) in the models
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(Iso-NTCP treatment plan individualisation could be a strategy to improve
clinical outcome
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Inclusion of deformation during the treatment (doses really absorbed in
the voxels, elastic match, shrinkage effects etc))