Single-agent treatment with the humanized monoclonal antibody trastuzumab (
herceptin) has shown remarkable activity in patients with metastatic breast
cancer overexpressing the HER-2/neu proto-oncogen. Further significant adv
ances could be achieved with the combined use of herceptin and paclitaxel o
r doxorubicin/cyclophosphamide. However, cardiotoxicity remains a significa
nt and thus far unresolved problem of the herceptin-doxo-rubicin combinatio
n. Thus, several studies have recently been initiated to identify equally e
ffective but less toxic first-line regimens. Epirubicin, the taxanes paclit
axel and docetaxel, Navelbine(R), cisplatin, and Caelyx(R), a liposomal enc
apsulated formulation of doxorubicin, were selected for combination with he
rceptin in these studies because the appeared the most promising agents.