RANDOMIZED PHASE-II STUDY OF A COMBINATION OF CISPLATIN (DDP), 5-FLUOROURACIL (5-FU), AND ALLOPURINOL (HPP) VERSUS 5-FU IN ADVANCED COLORECTAL-CARCINOMA - AN EORTC GASTROINTESTINAL-TRACT CANCER COOPERATIVE GROUP-STUDY

In order to improve the therapeutic index of fluorouracil (5-FU), it has been combined with cisplatin (DDP) as synergistic agent and with allopurinol (HPP) as toxicity modulator. Patients with measurable colorectal carcinoma, previously untreated by chemotherapy, were randomized to receive either 5-FU alone 500 mg/m2 push iv days 1-5 or HPP 3 x 300 mg po, days 1-5, 5-FU 800 mg/m2 push iv, days 3-5 and DDP 50 mg/m2 d6. Treatment was repeated every 4 weeks. Of 104 patients randomized, 82 were evaluable for response and survival. Six partial responses were seen in each treatment group (15%) and the median survival time was 7 months. Hematologic toxicities were comparable in both treatment groups, with a mean nadir white blood cell count of 3500/ vs. 3800/mm3 and a mean nadir platelet count of 148,000/ vs. 203,000/mm3 for HPP-5FU-DDP and 5-FU, respectively. This study suggests that the addition of both HPP and DDP does not improve the activity of 5-FU.