There has been much progress in the understanding of the relationship betwe
en the immune system and colorectal cancer: This has led to the use of immu
nomodulatory therapy in the adjuvant and palliative treatment of the condit
ion. Although attempts at the use of non-specific immunomodulation with age
nts such as levamisole, cimetidine, alpha interferon and Bacillus Calmette-
Guerin (BCG) have not produced significant clinical benefits when tested in
randomized trials in both the adjuvant setting and for metastatic disease.
promising results are being obtained with more specific therapy. Edrocolom
ab, a murine monoclonal antibody targeting the 17-IA antigen on malignant c
olorectal cells has produced a reduction in relapse and mortality rates whe
n used as adjuvant treatment following surgery for Dukes' C colon cancer: A
ctive specific therapy with autologous tumour Vaccine administered with BCG
has produced similar benefits in Dukes' B cancer: Both 3HI antiidiotypic a
ntibody against carcinoembryonic antigen and 105AD7 antibody to gp72 glycop
rotein have demonstrated in-vitro and in-vivo immune activation against tum
our. Non-randomized studies postulate prolongation of survival using these
antibodies in advanced disease. These agents are all currently being tested
in randomized studies powered to detect meaningful survival differences an
d clinical benefit. immune therapy offers the potential of low toxicity the
rapy in colorectal cancer and may have a role as an adjunct to conventional
chemotherapy. (C) 2000 Harcourt Publishers Ltd.