Cardiac toxicity is frequently the indication for discontinuation of an ant
hracycline in patients with tumors which remain anthracycline-sensitive. Du
ring the 1990s, the most frequently used second-line agents at the Yale Can
cer Center (YCC) were the taxanes. The goal of this retrospective analysis
was to determine the effect of paclitaxel on cardiac function in patients w
ith cardiomyopathy. YCC outpatient clinic pharmacy order forms were used to
identify all patients who had received paclitaxel between December 1995 an
d November 1997. The clinic records of those patients with a left ventricul
ar ejection fraction (LVEF) of less than or equal to 50% were reviewed to d
etermine the temporal relation between the decreased LVEF and paclitaxel th
erapy. In addition, clinic records were examined for evidence of prior doxo
rubicin therapy and history of prior cardiac disease. Between December 1995
and November 1997, 225 patients were treated with paclitaxel in the YCC ou
tpatient clinic. Nine patients had LVEF less than or equal to 50% (mean 37%
) prior to initiation of paclitaxel therapy. Six of these patients had equi
librium radionuclide angiocardiographic (ERNA) scans following completion o
f paclitaxel, In these 6 patients, the mean change in LVEF was +6% (range -
3% to +29%). Four patients had improved LVEF following paclitaxel (mean 11%
, range 2% to 29%), while 2 patients experienced a decrease in LVEF followi
ng paclitaxel treatment (mean 2.5%). The 3 patients who did not have ERNA s
cans following paclitaxel therapy had no clinical evidence of congestive he
art failure. Our experience confirms the results of prior studies that pacl
itaxel can be safely administered in patients with underlying cardiac dysfu
nction. (C) 2001 Wiley-Liss, Inc.