After studies in preclinical mouse models, the efficacy acid safety of tumo
r-specific vaccination strategies is currently being evaluated in cancer pa
tients, The first wave of clinical trials has shown that in general such va
ccination strategies are safe. However examples of clinical responses, espe
cially in conjunction with vaccine-induced immune responses, are still scar
ce. The fact that most trials have so far been performed with end-stage can
cer patients can largely account for this deficit. Greater efficacy of anti
cancer vaccines is expected in patients with less-progressed disease. In ad
dition, the detection of both natural and vaccine-induced T cell immunity n
eeds further improvement.