New photosensitising drugs are becoming available which should improve
on some of the disadvantages of haematoporphyrin derivates for photod
ynamic therapy (PDT). The main features are shorter duration of system
ic photosensitisation, activation by longer and more penetrating tight
and better tumour to normal tissue drug uptake ratios. These drugs to
gether with better understanding of in vivo light dosimetry promise to
improve both results and clinical acceptability for PDT in future stu
dies.