Standard treatments for adenocarcinoma of the prostate, such as surgery, ho
rmones, radiation and chemotherapy, often achieve a clinical response, but
this is usually short-lived. Prostate cancer frequently recurs and second-l
ine therapies have a poor response rate. Many clinicians seem comfortable i
n limiting their philosophy of treating advanced recurrent disease merely t
o new regimens of failed therapies, such as combination chemotherapy. Howev
er, other medical researchers have chosen to pursue novel approaches, inclu
ding immunotherapy, several of which are summarised in this review. Althoug
h ranging widely in antigen specificity, all attempt to exploit the body's
natural antitumour immunity. Furthermore, all aim to stimulate immunity abo
ve a threshold level necessary for tumour regression or to induce stability
in the face of progression. The goal of in vivo or ex vivo gene therapy is
the modification of gene expression within an antigen-presented cell by th
e introduction of a vector, DNA, or RNA. Within that field, much progress h
as been made and is ongoing currently concerning gene delivery systems, tar
get identification and characterisation. Comparatively, monoclonal antibodi
es are an established type of cancer immunotherapy. However, the more recen
t development of humanised or fully human antibodies, as well as novel moie
ties they can be coupled to, renews their prospects for clinical impact. La
stly, various cell-based therapies are the focus of several recent clinical
studies demonstrating tumour regression or stabilisation. Immune cells, fo
r example, T-lymphocytes and dendritic cells, have already demonstrated tre
atment benefit, as well as the ability to maintain an excellent quality of
life for participants. Overall, there is a multitude of approaches being co
nsidered for the treatment of prostate cancer. The following review concent
rates on those approaches that are currently in human or animal studies and
have a specific emphasis on prostate cancer.