Chronic oral etoposide has shown activity in some metastatic refractor
y tumors. To test its activity in previously treated metastatic breast
cancer patients, we started a study in 18 consecutive patients given
etoposide orally at 50 mg/m(2) daily for 21 days. A partial response w
as observed in 4 of 18 patients (22%); of the responding patients, 3 h
ad visceral metastases and 1 had multiple bone metastases. Leukopenia
of grade 3 or 4 was the main hematological toxic effect (23% of patien
ts) and alopecia was the most important nonhematological toxicity. Chr
onic oral etoposide shows some activity in pretreated patients with me
tastatic breast cancer, with tolerance being good and toxicity, accept
able. Further studies of this drug given as first-line chemotherapy or
in combination with other drugs can establish all its potential activ
ity in this cancer.