The identification of hematopoietic growth factors and their production usi
ng recombinant techniques have led to clinical evaluation of their effectiv
eness in treating primary bone marrow failure states and the myelosuppressi
on caused by chemo- and radiotherapy. Granulocyte colony-stimulating factor
(G-CSF), granulocyte-macrophage colony-stimulating factor (GMCSF), erythro
poietin and, in phase I/II trials, thrombopoietin (TPO) and interleultin-11
(IL-11) are currently available for clinical use. Clinical studies perform
ed with G-CSF and GM-CSF have proven their beneficial effects in accelerati
ng hematopoietic recovery after chemotherapy. This results from a marked re
duction in the risk of infections and a shortening of drug and radiation in
duced myelosuppression. CSFs are most important in mobilizing peripheral bl
ood progenitor cells (PBPC) and have allowed high-dose therapy combined wit
h stem cell support in urological malignancies, e.g., refractory germ cell
tumors. In addition, CSFs play an important part in the modulation of respo
nses of circulating or tissue phagocytes to bacterial or fungal microorgani
sms. This important role has only recently begun to be eluciated. However,
evidence based, clinical practice guidelines for the use of hematopoietic g
rowth factors in urological malignancies, as well as for fever and infectio
n following cytostatic chemotherapy, have yet to be developed.