Effect of statins on the recurrence of hepatocellular carcinoma after liver transplantation: An illusion revealed by exposure density sampling

Author:

Kim Deok‐Gie1ORCID,Yim Seung Hyuk1ORCID,Min Eun‐Ki1ORCID,Choi Mun Chae1ORCID,Kim Myoung Soo1ORCID,Joo Dong Jin1ORCID,Lee Jae Geun1ORCID

Affiliation:

1. Department of Surgery The Research Institute for Transplantation, Yonsei University College of Medicine Seoul South Korea

Abstract

AbstractBackgroundStatins have been reported to reduce overall death and hepatocellular carcinoma (HCC) recurrence in liver transplantation (LT) recipients. However, previous retrospective studies have significant flaws in immortal time bias.MethodsUsing data from 658 patients who received LT for HCC, we matched 140 statin users with statin nonusers in a 1:2 ratio at the time of the first statin administration after LT using the exposure density sampling (EDS). The propensity score, calculated using baseline variables (including explant pathology), was used for EDS to equilibrate both groups. HCC recurrence and overall death were compared after adjusting for information at the time of sampling.ResultsAmong statin users, the median time to statin start was 219 (IQR 98–570) days, and intensity of statins was mainly moderate (87.1%). Statin users and nonusers sampled using EDS showed well‐balanced baseline characteristics, including detailed tumour pathology, and similar HCC recurrence with cumulative incidences of 11.3% and 11.8% at 5 years, respectively (p = .861). In multivariate Cox models (HR 1.04, p = .918) and subgroup analyses, statins did not affect HCC recurrence. Conversely, statin users showed a significantly lower risk of overall death than nonusers (HR 0.28, p < .001). There was no difference in the type and intensity of statin usage between statin users who experienced HCC recurrence and those who did not.ConclusionUpon controlling immortal time bias by EDS, statins did not affect HCC recurrence but reduced mortality after LT. Statin usage is encouraged for survival benefits but not for preventing HCC recurrence in LT recipients.

Publisher

Wiley

Subject

Hepatology

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