Gene therapy is a rapidly evolving concept for the therapy of differen
t forms of cancer: A number of phase-I clinical trials have recently b
een initiated world wide. This review discusses the technical concepts
underlying the protocols currently coming into clinics. Two tools ess
entially constitute such concepts, the vector for efficient transfer a
nd expression of the transgene in the cancer cell, and the therapeutic
gene. The most advanced vectors ready for clinical use are the retrov
irus- and adenovirus-derived vectors. The application of a broad spect
rum of therapeutic genes can be classified into gene replacement of re
place e.g. mutated tumor suppressor genes, gene addition to increase i
mmunogenicity by cytokine genes or introduce prodrug genes for suicide
induction and, thirdly, targeted affection of gene expression by anti
sense oligonucleotides or expression of ribozymes e.g. directed agains
t oncogene sequences. Cancer gene therapy holds great promise to becom
e an important addition to the multimodality in the therapy of some fo
rms of cancer.