N. Brock et J. Pohl, Development of oncological therapeutic agents - Current state and outlook with special regard to the situation in Germany, ARZNEI-FOR, 50(10), 2000, pp. 946-953
The development of oncological therapeutic agents is a complex and risky pr
ocess and it is mainly pursued by research-based pharmaceutical companies.
Academic and public research institutions, however, have contributed to the
finding and evaluation of basic scientific knowledge, which were transferr
ed to the industry for co-development. Since 1960 increasing regulatory dem
ands have caused a prolonged development time and dramatical multiplication
of costs.
Oncological research in Germany began shortly after the end of war, when Pa
yer worked on the ethyleneimino compounds with agents like E39 and trenimon
for therapeutical use. Early in the fifties this focus of research changed
to Asta-Werke, Bielefeld (later ASTA Medica, Frankfurt) where cyclophospha
mide (Endoxan(R), Cytoxan(R)), ifosfamide (Holoxan(R), Ifexo) and trofosfam
ide were developed as worldwide leading alkylating cytotoxic agents. The de
tection of mesna (Uromitexan(R), Mesnex(R)) used for the organospecific det
oxification of urotoxic metabolites caused a further increase of the cancer
otoxic selectivity and an improved safety of oxazaphosphorine therapy. Ther
e has been ongoing research on alkylating agents (mafosfamide, glufosfamide
), and new therapeutic principles like miltefosine (Miltex(R)) or hormonal
agents like cetrorelix (LHRH-antagonist) are in development.