G. Arcangeli et al., A PILOT-STUDY OF CONCOMITANT PROTRACTED VENOUS INFUSION 5-FLUOROURACIL AND HYPERFRACTIONATED RADIOTHERAPY IN RECTAL TUMORS, American journal of clinical oncology, 18(5), 1995, pp. 369-375
It has recently been shown that postoperative radiotherapy combined wi
th 5-fluorouracil (5FU) resulted in an increase of survival and local
control in patients with rectal cancer. However, hematological and int
estinal toxicity were also increased. Experimental and clinical studie
s showed an increased radiation effect with an acceptable toxicity by
delivering 5FU via a continuous intravenous infusion. From July 1988,
38 patients radically operated on for stages B2-C rectal cancer were i
rradiated in our hospital with 3 fractions per day of 100 cGy to a tot
al dose of 5,600 cGy. Of these 38 patients, 13 underwent postoperative
radiotherapy alone, and 25 received postoperative radiotherapy combin
ed with concomitant protracted infusion of 5FU at doses of 250 and 300
mg/m(2) per day. In addition, 14 patients with inoperable, locally ad
vanced tumors or postoperative recurrences, were treated with the same
combination schedule of 5FU and radiotherapy to a total radiation dos
e of 6,500 cGy. After a median follow-up of 43 months, the actuarial 3
-year overall and disease-free survival rates in the postoperative gro
up of patients were 68% and 68%, respectively, in the combined modalit
y group, as compared to 51% and 36%, respectively, in the radiation al
one group. Patients with inoperable tumors exhibited 3-year overall an
d disease-free survival rates of 24% and 32%, respectively. The main t
oxicity was rectal tenesmus, diarrhea, dysuria, and, less frequently,
leukopenia. These symptoms were responsible for a treatment delay of m
ore than 5 days in 2 of 6 and in 7 of 33 patients who received 5FU dos
es of 300 and 250 mg/m(2) per day, respectively, as compared to 2 of 1
3 patients treated with radiotherapy alone.