E. Staibsebler et al., CONTINUOUS ARTERIAL 5-FLUOROURACIL AND FOLINIC ACID CHEMOTHERAPY FOR COLORECTAL LIVER METASTASES, Onkologie, 18(3), 1995, pp. 240-244
Background: A liver resection is only possible for about 20% of all pa
tients suffering from liver metastases from colorectal cancer. Alterna
tively, intra-arterial chemotherapy is an attractive treatment against
non-resectable isolated liver metastases, though this is not a proven
method to date. Aim: As an alternative to the FUDR fluorodesoxyuridin
e) therapy with its high local toxicity, we assessed a regional therap
y with 5-FU (fluorouracil) using the modulation with FA (folinic acid)
as a continuous application. Patients and Methods: In 16 patients wit
h non-resectable liver metastases an intra-arterial port was implanted
to carry out the ambulant chemotherapy. The intra-arterial catheter w
as placed after explorative laparotomy across the gastroduodenal arter
y with the tip tangential to the hepatic artery. The initial dose tota
lled to 1,000 mg/m(2) body surface 5-FU and 200 mg/m(2) FA. 5-FU was a
pplied continuously for 5 days simultaneously with FA as a daily short
infusion. The therapy was repeated every 28 days. A total of 115 cycl
es was evaluated according to WHO grading. Results: The therapy was as
sociated with the following non-haematological side-effects (WHO grade
2-3): stomatitis (52%), nausea/vomiting (12%), diarrhea (11%), pain (
3%), skin reaction (7%), hair loss (3%). The dose has to be reduced af
ter the first cycle in 6 patients due to grade 3 toxicity. The respons
e rates were: complete remission 2 patients, partial remission 7 patie
nts, stable disease 4 patients, progression 3 patients. The median sur
vival time of the 16 patients was 24 months. Progression occurred afte
r a median time of 16 months.Conclusion: This study shows the effectiv
ity of ambulant continuous 5-FU/FA application with controllable syste
mic side-effects without local toxicity. The demonstrated high rate of
complete plus partial response rate and extended survival rate should
be evaluated in a randomized trial with systemic treatment.