A significant number of women with advanced breast cancer fail to respond t
o standard-dose chemotherapy. From the beginning of 1999, 17 women with HER
2 positive advanced breast cancer received Herceptin(R) as monotherapy or i
n combination with paclitaxel or other non-anthracyclines. Eight (47%) wome
n previously received high-dose chemotherapy followed by haematopoiesis ste
m cell rescue. Three women received Herceptin(R) alone, eleven Herceptin(R)
plus paclitaxel and three Herceptin(R) and some of other non-anthracycline
s (CCNU, cisplatin and gemcitabine). In the group of patients who received
Herceptin(R) monotherapy, one has partial response (PR), one stable disease
(SD) and in the third patient the disease progressed. Out of three patient
s who received Herceptin(R) in combination with other non-anthracyclines, t
wo have SD and one progressed. In the group of 11 women who received Hercep
tin(R) + Taxol(R), 7 (64%) patients achieved PR, 2 (18%) SD, and 2 (18%) ha
d disease progression. Grade 3-4 neutropenia has been observed in four (23%
) women. Febrile neutropenia was observed in two cases and resolved complet
ely when antibiotics were introduced. Other grade 3 toxicity that has been
noted is peripheral neuropathy in three (18%) patients, diarrhoea in four (
23%) and onycholysis in one (6%). Serial heart ultrasound showed no signifi
cant decline in left ventricular ejection fraction. According to our prelim
inary experience, Herceptin(R) therapy showed promising results in women wi
th metastatic breast cancer.