Adjuvant chemotherapy improves the disease-free and overall survival o
f patients with resectable, early-stage breast cancer. However. the ef
fect is modest, and we need means of increasing its impact. Retrospect
ive and prospective studies on the effects of increased drug dosage ha
ve demonstrated that within some dose ranges, increasing the dose inte
nsity (total drug dose divided by total treatment time) improves the o
utcome of treatment. Dose escalation to higher levels, sufficient to r
equire growth factor and autologous stem cell support, is the subject
of ongoing randomized study. Because there are both theoretical and pr
actical limits on the potential effectiveness of single-cycle, high-do
se chemotherapy researchers are developing alternative means of increa
sing the effect of chemotherapy. One theoretically advantageous approa
ch, predicted to be superior by kinetic models, is ''dose-dense'' chem
otherapy administration. This approach consists of multiple cycles of
escalated-dose chemotherapy administered at very short intervals. When
administering presumed non-cross-resistant regimens or agents with ov
erlapping toxicity, clinicians can increase dose density by using the
sequential treatment plan. Furthermore, this plan can also facilitate
the addition of new active drugs.