Author/Authors :
Josep M. Llovet، نويسنده , , Maria Isabel Real، نويسنده , , Xavier Monta?a، نويسنده , , Ramon Planas، نويسنده , , Susana Coll، نويسنده , , John Aponte، نويسنده , , Carmen Ayuso، نويسنده , , Margarita Sala، نويسنده , , Jordi Muchart، نويسنده , , Ricard Solà، نويسنده , , Joan Rodes، نويسنده , , Jordi Bruix and for the Barcelona Cl?nic Liver Cancer Group، نويسنده ,
Abstract :
Background
There is no standard treatment for unresectable hepatocellular carcinoma. Arterial embolisation is widely used, but evidence of survival benefits is lacking.
Methods
We did a randomised controlled trial in patients with unresectable hepatocellular carcinoma not suitable for curative treatment, of Child-Pugh class A or B and Okuda stage I or II, to assess the survival benefits of regularly repeated arterial embolisation (gelatin sponge) or chemoembolisation (gelatin sponge plus doxorubicin) compared with conservative treatment. 903 patients were assessed, and 112 (12%) patients were finally included in the study. The primary endpoint was survival. Analyses were by intention to treat.
Findings
The trial was stopped when the ninth sequential inspection showed that chemoembolisation had survival benefits compared with conservative treatment (hazard ratio of death 0•47 [95% CI 0•25–0•91], p=0•025). 25 of 37 patients assigned embolisation, 21 of 40 assigned chemoembolisation, and 25 of 35 assigned conservative treatment died. Survival probabilities at 1 year and 2 years were 75% and 50% for embolisation; 82% and 63% for chemoembolisation, and 63% and 27% for control (chemoembolisation vs control p=0•009). Chemoembolisation induced objective responses sustained for at least 6 months in 35% (14) of cases, and was associated with a significantly lower rate of portal-vein invasion than conservative treatment. Treatment allocation was the only variable independently related to survival (odds ratio 0•45 [95% CI 0•25–0•81], p=0•02).
Interpretation
Chemoembolisation improved survival of stringently selected patients with unresectable hepatocellular carcinoma.