Immunotoxins (monoclonal antibodies chemically coupled to peptide toxi
ns) and fusion toxins (peptide ligands fused genetically to peptide to
xins) have been used to treat a variety of malignancies over the East
20 years. Problems with normal tissue toxicities (vascular leak syndro
me, hepatotoxicity, and neurotoxicities), poor penetration to tumor in
terstitum, and humoral immune responses have limited clinical efficacy
. Higher response rates were observed with systemic therapy of leukemi
as and lymphomas and regional therapy of primary brain tumors. Ongoing
studies are examining the role of targeted toxins in combination with
chemoradiotherapy and in minimal residual disease settings. (C) 1995
Academic Press Ltd