The use of dose-dense therapy is one approach to overcoming the ''resi
stance'' of malignant cells to adjuvant therapy caused by inadequate d
rug exposure. In this approach, active drugs are delivered sequentiall
y at their ''ideal'' dose level separated by short intertreatment inte
rvals. Thus, dose intensification is achieved by means of rapidly recy
cled treatments rather than by dramatic dose escalation. To overcome a
bsolute cellular resistance, the addition of new, active, non-cross-re
sistant drugs holds great promise and has specifically motivated the t
esting of the taxanes. This article describes the results of clinical
trials of dose-dense therapy, with particular emphasis on attempts to
incorporate one taxane, paclitaxel (Taxol), into the dose-dense regime
n of sequential doxorubicin and cyclophosphamide-the so-called A --> T
--> C regimen, and into more conventional regimens.