A randomised multicentre phase II trial of capecitabine vs S-I as first-line treatment in elderly patients with metastatic or recurrent unresectable gastric cancer

This randomised multicentre phase II study was conducted to investigate the activity and safety of two oral fluoropyrimidines, capecitabine or S-I, in elderly patients with advanced gastric cancer (AGC). Elderly (>= 65 years) chemo-naive patients with AGC were randomly assigned to receive capecitabine 1250 mg m(-2) two times daily on days 1-14 every 3 weeks or S-I 40 - 60 mg two times daily according to body surface area on days 1 - 28 every 6 weeks. Ninety-six patients were enrolled and 91 patients were randomised to capecitabine (N=46) or S-I (N=45). Overall response rate, the primary end point, was 27.2% ( 95% CI, 14.1 - 40.4, 12 of 44 assessable patients) with capecitabine and 28.9% ( 95% CI, 15.6 - 42.1, 13 of 45) with S-I. Median times to progression and overall survival in the capecitabine arm (4.7 and 9.5 months, respectively) were similar to those in the S-I arm (4.2 and 8.2 months, respectively). The incidence of grade 3 - 4 granulocytopenia was 6.8% with capecitabine and 4.8% with S-I. Grade 3 - 4 nonhaematologic toxicities were: asthenia (9.1% with capecitabine vs 7.1% with S-I), anorexia (6.8 vs 9.5%), diarrhoea (2.3 vs 0%), and hand - foot syndrome (6.8 vs 0%). Both capecitabine and S-I monotherapies were active and tolerable as first-line treatment for elderly patients with AGC.