Lanreotide Reduces the Volume of Polycystic Liver: A Randomized, Double-Blind, Placebo-Controlled Trial
Background & aims
Therapy for polycystic liver is invasive, expensive, and has disappointing long-term results. Treatment with somatostatin analogues slowed kidney growth in patients with polycystic kidney disease (PKD) and reduced liver and kidney volume in a PKD rodent model. We evaluated the effects of lanreotide, a somatostatin analogue, in patients with polycystic liver because of autosomal-dominant (AD) PKD or autosomal-dominant polycystic liver disease (PCLD).
Methods
We performed a randomized, double-blind, placebo-controlled trial in 2 tertiary referral centers. Patients with polycystic liver (n = 54) were randomly assigned to groups given lanreotide (120 mg) or placebo, administered every 28 days for 24 weeks. The primary end point was the difference in total liver volume, measured by computerized tomography at weeks 0 and 24. Analyses were performed on an intention-to-treat basis.
Results
Baseline characteristics were comparable for both groups, except that more patients with ADPKD were assigned to the placebo group (P = .03). The mean liver volume decreased 2.9%, from 4606 mL (95% confidence interval (CI): 547–8665) to 4471 mL (95% CI: 542–8401 mL), in patients given lanreotide. In the placebo group, the mean liver volume increased 1.6%, from 4689 mL (95% CI: 613–8765 mL) to 4895 mL (95% CI: 739–9053 mL) (P < .01). Post hoc stratification for patients with ADPKD or PCLD revealed similar changes in liver volume, with statistically significant differences in patients given lanreotide (P < .01 for both diseases).
Conclusions
In patients with polycystic liver, 6 months of treatment with lanreotide reduces liver volume.
Abbreviations used in this paper: ADPKD, autosomal dominant polycystic kidney disease, cAMP, cyclic adenosine monophosphate, CT, computerized tomography, GGT, γ-glutamyl transferase, HRQoL, health-related quality of life, PCK, polycystic kidney, PCLD, polycystic liver disease, PKD, polycystic kidney disease
To access this article, please choose from the options below
To view this article's video abstract, go to the AGA's YouTube Channel.
Conflicts of interest The authors disclose the following: Robert A. de Man: consulting and lecture fees and grant support from Gilead Sciences, consulting fees and grant support from Bristol–Myers Squibb, consulting fees from Novartis, and lecture fees from UCB. Joost P. H. Drenth: grant/research support from Roche. The remaining authors disclose no conflicts.
Funding Supported by Ipsen, Boulogne Billancourt, France, and a ZON-MW VIDI research grant (J.P.H.D.).
PII: S0016-5085(09)01377-8
doi:10.1053/j.gastro.2009.07.052
© 2009 AGA Institute. Published by Elsevier Inc. All rights reserved.

