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Summarising

Models to convert dose distributions into clinical outcome

exist and have been verified in certain cases (e.g. rectum,

lung, liver)

Care must taken if extending the application outside the

range where the parameter-fitting has been done

If possible, take into account the weight of the clinical

variables (including the genetic ones) in the models

(Iso-NTCP treatment plan individualisation could be a strategy to improve

clinical outcome

Inclusion of deformation during the treatment (doses really absorbed in

the voxels, elastic match, shrinkage effects etc))