BACKGROUND. The authors reviewed the incidence of toxic skin reactions
in patients with metastatic breast carcinoma (MBC) treated with vinor
elbine as a continuous infusion. METHODS. A Phase I/II protocol was de
signed in which vinorelbine was given as an 8-mg intravenous bolus fol
lowed by a 96-hour CI of 7-14 mg/m(2)/day. Sixty patients were enrolle
d in the study: all had MBC and had received prior chemotherapy, and t
hey had no known dermatologic disorder. RESULTS. Hand-foot syndrome (H
FS) developed in 4 of the 60 patients. Patient 1 started with vinorelb
ine at 12 mg/m(2)/day. She developed typical HFS. In the second course
, her dose was decreased to 11 mg/m(2)/day, but again she experienced
HFS. In the third course, dexamethasone was added to the regimen, and
no HFS was observed in the remaining six courses. Patient 2 started wi
th a dose of 9 mg/m(2)/day. She received four courses without complica
tions; but when the vinorelbine dose was escalated to 10 mg/m(2)/day.
HFS developed. Patient 3 started with a vinorelbine dose of 14 mg/m(2)
/day. She developed mucositis during the first two courses and HFS dur
ing the third. Patient 4 received vinorelbine at a dose of 13 mg/m(2)/
day and developed significant HFS. All patients had complete dermatolo
gic recovery. No toxic skin reactions were observed in 14 patients rec
eiving vinorelbine doses of <10 mg/m(2)/day, whereas 4 of 46 treated a
t 10-14 mg/m(2)/day developed HFS, suggesting a relationship of dose t
o I-IFS occurrence. CONCLUSIONS, Longer infusions of vinorelbine are o
ccasionally associated with HFS. The pathophysiology is not completely
clear, but a relationship of HFS occurrence to dose is suggested. Ste
roids were effective as prophylaxis in one patient. (C) 1998 American
Cancer Society.