Drug targeting is an attractive new approach to killing cancer cells w
hile leaving normal tissue unharmed. Recently we have developed a new
generation of antibody-targeted immunosuppressive (cyclosporin A) and
cytostatic (daunomycin, doxorubicin) drugs and photosensitizers (chlor
in e(6)) effective in vitro and in vivo. The drugs and the targeting a
ntibody (polyclonal and monoclonal) are conjugated to the oligopeptidi
c side chains of a water-soluble synthetic carrier, copolymer of N-(2-
hydroxypropyl)methacrylamide. The composition of the side chains ensur
es the stability of the linkage between the drug and the polymeric car
rier in the bloodstream and its intralysosomal degradability which is
a prerequisite for the pharmacological activity of the preparation. An
tibody-targeted polymer bound drugs show considerably decreased hepato
toxicity, cardiotoxicity, myelotoxicity and nephrotoxicity. Two adriam
ycin-HPMA copolymers are in Phase I/II clinical trials in United Kingd
om.