Mv. Madden et al., RANDOMIZED TRIAL OF TARGETED CHEMOTHERAPY WITH LIPIODOL AND 5-EPIDOXORUBICIN COMPARED WITH SYMPTOMATIC TREATMENT FOR HEPATOMA, Gut, 34(11), 1993, pp. 1598-1600
Lipiodol injected into the hepatic artery is selectively retained in h
epatomas so has been used as a vehicle for cytotoxic drugs. This study
compared treatment with 5-epidoxorubicin emulsified in lipiodol and i
nfused into the hepatic artery with symptomatic treatment alone in a r
andomised trial. Of 136 patients with hepatoma 78 (57%) were not elegi
ble, eight (6%) refused to take part, and 50 entered the trial (chemot
herapy: n=25, symptomatic treatment: n=25). The two groups had similar
prognostic indices. Seven of 25 patients allocated to chemotherapy we
re unable to receive it. The slight survival disadvantage associated w
ith chemotherapy was not significant (median survival 48 days compared
with 51 days, log rank chi2 =0.07, p>0.05). Patients given chemothera
py spent significantly longer in hospital, however (median three days
compared with one, p=0.0008). Changes in symptoms and indices of tumou
r growth did not differ significantly between the two groups. It is co
ncluded that infusion of 5-epidoxorubicin emulsified in lipiodol for h
epatoma increased morbidity but did not affect survival. In addition,
most patients were unsuitable for this treatment because of advanced d
isease. The patients in the trial had a short median survival time so
the conclusions may not be valid for other patients with hepatoma.