A RANDOMIZED PHASE-II STUDY OF ACIVICIN AND 4'DEOXYDOXORUBICIN IN PATIENTS WITH HEPATOCELLULAR-CARCINOMA IN AN EASTERN COOPERATIVE ONCOLOGY GROUP-STUDY

We analyzed 56 of 75 previously untreated patients with hepatocellular carcinoma who entered on a prospectively randomized trial of acivicin versus 4'deoxydoxorubicin (esorubicin). At least one episode of severe toxicity was documented in 23% of the patients on acivicin and 45% of those on 4'deoxydoxorubicin. Two patients responded to 4'deoxydoxorubicin. One response was partial, lasting 58 weeks, and one was complete, lasting more than 4 years. The 90% confidence interval for response is 1-20%. In view of a 45% rate of severe or worse toxicity with 4'deoxydoxorubicin, this drug cannot be recommended as treatment. There were no responses on acivicin.