Journal of Clinical Oncology, Vol 8, 2027-2031, Copyright © 1990 by American Society of Clinical Oncology
Phase II study of fluorouracil and recombinant interferon alfa-2a in previously untreated advanced colorectal carcinoma
R Pazdur, JA Ajani, YZ Patt, R Winn, D Jackson, B Shepard, R DuBrow, L Campos, M Quaraishi and J Faintuch
Department of Medical Oncology, University of Texas MD Anderson Cancer Center, Houston 77030.
We conducted a phase II clinical trial of fluorouracil (5FU) and
recombinant interferon alfa-2a (rIFN alpha-2a) in 52 previously untreated
patients with bidimensionally measurable metastatic colorectal cancer.
During week 1, 5FU was administered as a continuous intravenous infusion,
750 mg/m2/d for 5 consecutive days. Intravenous bolus administration of 5FU
750 mg/m2 was given weekly for 7 weeks starting on day 12. rIFN alpha-2a
(Roferon; Hoffman-LaRoche, Nutley, NJ), 9 x 10(6) U, was administered
subcutaneously three times weekly during weeks 1 to 8. Patients were
evaluated for response on week 9. Of 52 patients enrolled in the study, 51
were assessable for toxicity, and 45 were assessable for response. Fifteen
patients experienced partial response, and one patient achieved a clinical
complete response for an overall response rate of 35% (95% confidence
interval [CI], 22%, 50%). Median duration of response is 7.5 months (range,
4 to 11 months). Seventy percent of patients entered on the study are alive
with a median follow-up duration of 7 months. Twenty-five percent of
patients developed grade 4 toxicity, and 82% developed grade 3 toxicity.
One drug-related death in the presence of sepsis was reported, and two
treatment-related seizures occurred. Our experience with this schedule
produced a lower response rate with greater toxicity than previously
reported. Current randomized trials comparing this schedule of 5FU with
rIFN alpha-2a to 5FU plus folinic acid (leucovorin) or single-agent 5FU may
determine its role in the treatment of advanced colorectal carcinomas.