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Article

Increased Visceral Adipose Tissue and Hyperinsulinemia Raise the Risk for Recurrence of Non-B Non-C Hepatocellular Carcinoma after Curative Treatment

Department of Gastroenterology/Internal Medicine, Gifu University Graduate School of Medicine, 1-1 Yanagido, Gifu 501-1194, Japan
*
Author to whom correspondence should be addressed.
Cancers 2021, 13(7), 1542; https://doi.org/10.3390/cancers13071542
Submission received: 18 February 2021 / Revised: 18 March 2021 / Accepted: 24 March 2021 / Published: 26 March 2021
(This article belongs to the Special Issue Translational Studies of Obesity-Associated Hepatocellular Cancer)

Simple Summary

With the increasing prevalence of obesity and diabetes in most countries, the increase in hepatocellular carcinoma (HCC) associated with these factors has recently become a serious healthcare problem. HCC can often emerge in the non-cirrhotic liver among obese patients, and it might suggest that the conventional surveillance strategies for HCC, which is mainly targeted at cirrhotic patients with hepatitis B or C virus, might be insufficient in the overnutrition era. We tried to extract factors that affect recurrence-free survival in patients with non-viral HCC, among obesity and diabetes factors, together with the established recurrence risk factors, using a decision-tree analysis.

Abstract

We investigated the factors affecting recurrence-free survival in patients with non-B non-C hepatocellular carcinoma (HCC) who received curative treatment. Decision-tree analysis was performed in 72 curative cases of non-B non-C HCC to extract the risk factors for recurrence. The reliability of the extracted risk factors was evaluated using the Kaplan–Meier method and the Cox proportional hazards model. The decision-tree analysis extracted three factors—visceral adipose tissue (VAT) index (VATI; <71 and ≥71 cm2/m2), which was the cross-sectional areas of VAT on the computed tomographic image at the umbilical level, normalized by the square of the height, fasting immunoreactive insulin (FIRI; <5.5 and ≥5.5 µU/mL), and alpha-fetoprotein (AFP; <11 and ≥11 ng/mL). The Cox proportional hazards model showed that VATI (hazard ratio (HR): 2.556, 95% confidence interval (CI): 1.191–5.486, p = 0.016), FIRI (HR: 3.149, 95% CI: 1.156–8.575, p = 0.025), and AFP (HR: 3.362, 95% CI: 1.550–7.288, p = 0.002) were all independent risk factors for HCC recurrence. Non-B non-C HCC patients with a higher VATI (≥71 cm2/m2) or higher FIRI (≥5.5 µU/mL) and AFP (≥11 ng/mL) if VATI was <71 cm2/m2 are prone to recurrence after curative treatment.
Keywords: fasting immunoreactive insulin; non-viral hepatocellular carcinoma; recurrence risk factor; visceral adipose tissue fasting immunoreactive insulin; non-viral hepatocellular carcinoma; recurrence risk factor; visceral adipose tissue

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MDPI and ACS Style

Imai, K.; Takai, K.; Miwa, T.; Maeda, T.; Hanai, T.; Shiraki, M.; Suetsugu, A.; Shimizu, M. Increased Visceral Adipose Tissue and Hyperinsulinemia Raise the Risk for Recurrence of Non-B Non-C Hepatocellular Carcinoma after Curative Treatment. Cancers 2021, 13, 1542. https://doi.org/10.3390/cancers13071542

AMA Style

Imai K, Takai K, Miwa T, Maeda T, Hanai T, Shiraki M, Suetsugu A, Shimizu M. Increased Visceral Adipose Tissue and Hyperinsulinemia Raise the Risk for Recurrence of Non-B Non-C Hepatocellular Carcinoma after Curative Treatment. Cancers. 2021; 13(7):1542. https://doi.org/10.3390/cancers13071542

Chicago/Turabian Style

Imai, Kenji, Koji Takai, Takao Miwa, Toshihide Maeda, Tatsunori Hanai, Makoto Shiraki, Atsushi Suetsugu, and Masahito Shimizu. 2021. "Increased Visceral Adipose Tissue and Hyperinsulinemia Raise the Risk for Recurrence of Non-B Non-C Hepatocellular Carcinoma after Curative Treatment" Cancers 13, no. 7: 1542. https://doi.org/10.3390/cancers13071542

APA Style

Imai, K., Takai, K., Miwa, T., Maeda, T., Hanai, T., Shiraki, M., Suetsugu, A., & Shimizu, M. (2021). Increased Visceral Adipose Tissue and Hyperinsulinemia Raise the Risk for Recurrence of Non-B Non-C Hepatocellular Carcinoma after Curative Treatment. Cancers, 13(7), 1542. https://doi.org/10.3390/cancers13071542

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