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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))