肝细胞癌肝脏切除术后的预后因素--病理免疫分型的重要性、脂肪肝亚型和肝梗夹闭的影响

L. Viana, Rui Caetano Oliveira, R. Martins, H. Alexandrino, M. Cipriano, J. Tralhão
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引用次数: 0

摘要

简介肝切除术(HP)和肝移植是唯一可能治愈肝细胞癌(HCC)的治疗方法。代谢综合征(MS)的高发病率可能会导致 HCC 病谱发生变化。肝椎管钳夹术(HPC)用于减少 HP 术中的围手术期出血,理论上会增加复发风险。细胞角蛋白 19 (CK19) 和糖蛋白-3 (GLP-3) 已被确定为 HCC 预后较差的标志物。材料与方法:对 2005 年至 2013 年间接受 HP 治疗的 59 例 HCC 患者进行了临床和病理检查。53名患者(89.8%)患有慢性肝病,54.2%患有肝硬化[最常见的病因:乙型肝炎(47.5%)、丙型肝炎病毒(25.4%)和乙型肝炎病毒(11.9%)]。36%的患者患有多发性硬化。此外,95%的患者为 Child-Pugh A 级,5%为 B 级,MELD 中位数为 8(6-18)。46名患者(78%)观察到单个结节,平均大小为5.4厘米。49%的患者存在显微镜下血管侵犯(MiVI),17%的患者存在大血管侵犯(MaVI)。43例患者(74.1%)出现 HPC。统计分析使用 SPSS™ 21.0 进行。生存测试(Kaplan-Meier、log-rank和Cox回归)。统计意义以 p < 0.05 为准。结果22%的患者有重大疾病。死亡率为 5.1%。中位总生存期(OS)为 71 个月,中位无病生存期(DFS)为 37 个月。多变量分析显示MaVI(p = 0.001)、MiVI(p = 0.005)和HCV感染(p = 0.002)与较差的OS相关;MS与较好的OS相关(p = 0.001);MaVI(p = 0.000)、MiVI(p = 0.035)和HPC(p = 0.012)与较差的DFS相关。CK19+/GLP-3-(p = 0.007)和CK19-/GLP-3+(p = 0.029)患者的DFS较差,而CK19-/GLP-3-(p = 0.031)患者的DFS较好。讨论/结论:HPC是导致DFS恶化的一个独立因素。HPC产生的缺血再灌注损伤(IRI)可促进肿瘤细胞的血管生成和血管侵袭表型,从而导致复发率升高。HCV病因与较差的OS相关。MS与较好的OS相关,突出了肝切除术在这些病例中的重要性。CK19和GLP-3的联合检测是HCC患者的一个独立预后因素,有助于识别侵袭性更强的肿瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prognostic Factors after Hepatectomy for Hepatocellular Carcinoma—The Importance of Pathological Immunophenotyping, the Steatohepatitic Subtype and the Impact of the Hepatic Pedicle Clamping
Introduction: Hepatectomy (HP) is, along with liver transplantation, the only potentially curative treatment for Hepatocellular Carcinoma (HCC). The high prevalence of Metabolic Syndrome (MS) may be causing a shift in the HCC spectrum. Hepatic Pedicle Clamping (HPC), used to reduce perioperative bleeding during HP, has been theorized to increase the risk of recurrence. Cytokeratin 19 (CK19) and glypican-3 (GLP-3) have been identified as markers of worse prognosis in HCC. Materials and Methods: A clinical and pathological review of 59 patients undergoing HP for HCC between 2005 and 2013 was performed. Chronic liver disease was observed in 53 patients (89.8%), with cirrhosis in 54.2% [most frequent etiologies: ethylism (47.5%), HCV (25.4%) and HBV (11.9%)]. MS was in 36% of patients. In addition, 95% of patients had Child–Pugh class A and 5% class B, and there was a median MELD of 8 (6–18). A single nodule was observed in 46 patients (78%) with an average size of 5.4 cm. Microscopic vascular invasion (MiVI) was in 49% of patients and macroscopic (MaVI) in 17. HPC was in 43 patients (74.1%). Statistical analysis was performed with SPSS™ 21.0. Survival tests (Kaplan–Meier, log-rank and Cox regression). Statistical significance was with p < 0.05. Results: Major morbidity in 22% of patients. Mortality in 5.1%. Median overall survival (OS) of 71 months and median disease-free survival (DFS) of 37. In a multivariate analysis: MaVI (p = 0.001), MiVI (p = 0.005) and HCV infection (p = 0.002) were associated with worse OS; MS was associated with better OS (p = 0.001); MaVI (p = 0.000), MiVI (p = 0.035) and HPC (p = 0.012) were associated with worse DFS. CK19+/GLP-3− (p = 0.007) and CK19−/GLP-3+ (p = 0.029) patients were associated with worse DFS and CK19−/GLP-3− (p = 0.031) with better DFS. Discussion/Conclusions: HPC was an independent factor of worse DFS. The ischemia-reperfusion injury (IRI) produced by HPC could promote a more angiogenic and angioinvasive phenotype of tumor cells, resulting in higher recurrence. HCV etiology was associated with worse OS. MS was associated with better OS, highlighting the importance of a hepatectomy in these cases. The combined detection of CK19 and GLP-3 was an independent prognostic factor in HCC patients allowing for the identification of more aggressive tumors.
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