Perrella Alessandro, Caturano Alfredo, de Sio Ilario, Bellopede Pasquale, Maddaloni Adelaide, Vitale Luigi Maria, Rinaldi Barbara, Mormone Andrea, Izzi Antonio, Sbreglia Costanza, Bernardi Francesca Futura, Trama Ugo, Berretta Massimiliano, Galiero Raffaele, Vetrano Erica, Sasso Ferdinando Carlo, Franci Gianluigi, Marfella Raffaele, Rinaldi Luca
VII Department of Infectious Disease and Immunology, Ospedali dei Colli, P.O. D. Cotugno, 80131 Naples, Italy.
Department of Advanced Medical and Surgical Sciences, University of Campania "Luigi Vanvitelli", 80138 Naples, Italy.
J Clin Med. 2024 Sep 14;13(18):5474. doi: 10.3390/jcm13185474.
: Despite achieving a sustained virological response (SVR) with direct-acting antivirals (DAAs), an unexpected increase in the occurrence rate of hepatocellular carcinoma (HCC) has been observed among HCV-treated patients. This study aims to assess the long-term follow-up of HCV patients treated with DAAs who achieved an SVR to investigate the potential for late-onset HCC. : In this prospective multicenter study, we enrolled consecutive HCV patients treated with DAAs following Italian ministerial guidelines between 2015 and 2018. Exclusion criteria included active HCC on imaging, prior HCC treatment, HBV or HIV co-infection, or liver transplant recipients. Monthly follow-ups occurred during treatment, with subsequent assessments every 3 months for at least 48 months. Abdominal ultrasound (US) was performed within two weeks before starting antiviral therapy, supplemented by contrast-enhanced ultrasonography (CEUS), dynamic computed tomography (CT), or magnetic resonance imaging (MRI) to evaluate incidental liver lesions. : Of the 306 patients completing the 48-months follow-up post-treatment (median age 67 years, 55% male), all achieved an SVR. A sofosbuvir-based regimen was administered to 72.5% of patients, while 20% received ribavirin. During follow-up, late-onset HCC developed in 20 patients (cumulative incidence rate of 6.55%). The pattern of HCC occurrence varied (median diameter 24 mm). Multivariate and univariate analyses identified liver stiffness, diabetes, body mass index, and platelet levels before antiviral therapy as associated factors for late HCC occurrence. : Our findings suggest that late HCC occurrence may persist despite achieving SVR. Therefore, comprehensive long-term follow-up, including clinical, laboratory, and expert ultrasonography evaluations, is crucial for all HCV patients treated with DAAs.
尽管使用直接抗病毒药物(DAA)实现了持续病毒学应答(SVR),但在接受丙肝病毒(HCV)治疗的患者中,肝细胞癌(HCC)的发生率却意外增加。本研究旨在评估接受DAA治疗并实现SVR的HCV患者的长期随访情况,以调查迟发性HCC的可能性。
在这项前瞻性多中心研究中,我们纳入了2015年至2018年间按照意大利卫生部指南接受DAA治疗的连续性HCV患者。排除标准包括影像学检查显示的活动性HCC、既往HCC治疗史、乙肝或艾滋病毒合并感染,或肝移植受者。治疗期间每月进行随访,随后每3个月进行一次评估,至少持续48个月。在开始抗病毒治疗前两周内进行腹部超声(US)检查,并辅以对比增强超声(CEUS)、动态计算机断层扫描(CT)或磁共振成像(MRI),以评估偶然发现的肝脏病变。
在完成治疗后48个月随访的306例患者中(中位年龄67岁,55%为男性),所有患者均实现了SVR。72.5%的患者接受了基于索磷布韦的治疗方案,20%的患者接受了利巴韦林治疗。在随访期间,20例患者发生了迟发性HCC(累积发病率为6.55%)。HCC的发生模式各不相同(中位直径24mm)。多因素和单因素分析确定,抗病毒治疗前的肝脏硬度、糖尿病、体重指数和血小板水平是迟发性HCC发生的相关因素。
我们的研究结果表明,尽管实现了SVR,迟发性HCC仍可能发生。因此,对于所有接受DAA治疗的HCV患者,包括临床、实验室和专家超声评估在内的全面长期随访至关重要。