Ultrasonographic surveillance of hepatocellular carcinoma in cirrhosis: A randomized trial comparing 3- and 6-month periodicities

Jean–Claude Trinchet(Université Sorbonne Paris Nord), Cendrine Chaffaut(Inserm), Valérie Bourcier(Université Sorbonne Paris Nord), Françoise Degos(Délégation Paris 7), Jean Henrion(Hôpital de Jolimont), Hélène Fontaine(Université Paris Cité), Dominique Roulot(Université Sorbonne Paris Nord), Ariane Mallat(Université Paris-Est Créteil), Sophie Hillaire(Hôpital Foch), Paul Calès(Centre Hospitalier Universitaire d'Angers), Isabelle Ollivier(Centre Hospitalier Universitaire de Caen Normandie), Jean‐Pierre Vinel(Inserm), Philippe Mathurin(Centre Hospitalier Universitaire de Lille), Jean–Pierre Bronowicki(Centre Hospitalier Régional et Universitaire de Nancy), Valérie Vilgrain(Inserm), G. Nkontchou(Université Sorbonne Paris Nord), Michel Beaugrand(Université Sorbonne Paris Nord), Sylvie Chevret(Inserm)
Hepatology
December 1, 2010
Cited by 397Open Access
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Abstract

UNLABELLED: Detection of small hepatocellular carcinoma (HCC) eligible for curative treatment is increased by surveillance, but its optimal periodicity is still debated. Thus, this randomized trial compared two ultrasonographic (US) periodicities: 3 months versus 6 months. A multicenter randomized trial was conducted in France and Belgium (43 sites). Patients with histologically proven compensated cirrhosis were randomized into two groups: US every 6 months (Gr6M) or 3 months (Gr3M). For each focal lesion detected, diagnostic procedures were performed according to European Association for the Study of the Liver guidelines. Cumulative incidence of events was estimated, then compared using Gray's test. The prevalence of HCC ≤30 mm in diameter was the main endpoint. A sample size of 1,200 patients was required. A total of 1,278 patients were randomized (Gr3M, n = 640; Gr6M, n = 638; alcohol 39.2%, hepatitis C virus 44.1%, hepatitis B virus 12.5%). At least one focal lesion was detected in 358 patients (28%) but HCC was confirmed in only 123 (9.6%) (uninodular 58.5%, ≤30 mm in diameter 74%). Focal-lesion incidence was not different between Gr3M and Gr6M groups (2-year estimates, 20.4% versus 13.2%, P = 0.067) but incidence of lesions ≤10 mm was increased (41% in Gr3M versus 28% in Gr6M, P = 0.002). No difference in either HCC incidence (P = 0.13) or in prevalence of tumors ≤30 mm in diameter (79% versus 70%, P = 0.30) was observed between the randomized groups. CONCLUSION: US surveillance, performed every 3 months, detects more small focal lesions than US every 6 months, but does not improve detection of small HCC, probably because of limitations in recall procedures.


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