Lin Yen-Po, Wang Pei-Ming, Chuang Ching-Hui, Yong Chee-Chen, Liu Yueh-Wei, Huang Pao-Yuan, Yao Chih-Chien, Tsai Ming-Chao
School of Medicine, Chung-Shan Medical University, Taichung, Taiwan.
Department of Family Medicine, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung, Taiwan.
Front Oncol. 2022 Feb 2;12:816472. doi: 10.3389/fonc.2022.816472. eCollection 2022.
Non-B, non-C hepatocellular carcinoma (NBNC-HCC) may be related to metabolic syndrome, and the incidence of this tumor type is increasing annually. The definition of metabolic-associated fatty liver disease (MAFLD) proposed in 2020 may help to more accuratelyassess the association between metabolic syndrome and NBNC-HCC. However, this new concept has not yet been applied in NBNC-HCC research. Therefore, this study aimed to compare the clinicopathological characteristics of patients with NBNC-HCC and CHB-HCC diagnosed between 2009-13 and 2014-18, focusing on metabolic risk factors and the new concept of MAFLD.
Patients with BCLC-0/A-HCC who received curative hepatectomy between January 2009 and December 2018 were retrospectively assessed; the associations between clinicopathological characteristics and clinical outcomes of NBNC-HCC and CHB-HCC were analyzed by multivariate analysis.
Compared to patients diagnosed in 2009-13, the frequency of metabolic disorders in NBNC-HCC was significantly higher in 2014-18 [DM (=0.049), HTN (=0.004), BMI (=0.017) and MAFLD (=0.003)]; there was no significant change in patients with CHB-HCC. Moreover, CHB-HCC was an independent risk factor for HCC recurrence (HR, 1.339; 95% CI, 1.010-1.775, 0.043) and death (HR, 1.700; 95% CI, 1.017-2.842, =0.043) compared to NBNC-HCC.
Therisk of MAFLD, obesity, DM, and hypertension in patients with early-stage NBNC have significantly increased in recent years, thus metabolic syndrome should be monitored in this special population. Moreover, NBNC-HCC tend to had a better prognosis than CHB-HCC, probably due to their distinct clinicopathological features.
非B、非C型肝细胞癌(NBNC-HCC)可能与代谢综合征有关,且这种肿瘤类型的发病率逐年上升。2020年提出的代谢相关脂肪性肝病(MAFLD)的定义可能有助于更准确地评估代谢综合征与NBNC-HCC之间的关联。然而,这一新概念尚未应用于NBNC-HCC研究。因此,本研究旨在比较2009 - 13年和2014 - 18年诊断的NBNC-HCC和CHB-HCC患者的临床病理特征,重点关注代谢风险因素和MAFLD的新概念。
对2009年1月至2018年12月期间接受根治性肝切除术的BCLC-0/A期HCC患者进行回顾性评估;通过多因素分析分析NBNC-HCC和CHB-HCC的临床病理特征与临床结局之间的关联。
与2009 - 13年诊断的患者相比,2014 - 18年NBNC-HCC中代谢紊乱的发生率显著更高[糖尿病(=0.049)、高血压(=0.004)、体重指数(=0.017)和MAFLD(=0.003)];CHB-HCC患者无显著变化。此外,与NBNC-HCC相比,CHB-HCC是HCC复发(HR,1.339;95%CI,1.010 - 1.775,P = 0.043)和死亡(HR,1.700;95%CI,1.017 - 2.842,P = 0.043)的独立危险因素。
近年来,早期NBNC患者发生MAFLD、肥胖、糖尿病和高血压的风险显著增加,因此应在这一特殊人群中监测代谢综合征。此外,NBNC-HCC的预后可能比CHB-HCC更好,这可能归因于它们不同的临床病理特征。