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Clinical characteristics and prognosis of hepatocellular carcinoma patients with paraneoplastic syndromes.

机译:伴副肿瘤综合征的肝癌患者的临床特征和预后。

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BACKGROUND/AIMS: Hepatocellular carcinoma patients with paraneoplastic syndromes usually have a larger tumor volume and a higher serum alpha-fetoprotein. Whether the presence of paraneoplastic syndromes, such as hypercholesterolemia, hypoglycemia, hypercalcemia, and erythrocytosis in hepatocellular carcinoma patients is a significant prognostic factor in patients' survival is of clinical interest. METHODOLOGY: We evaluated the occurrence of paraneoplastic syndromes in 903 hepatocellular carcinoma patients; 179 (20%) patients developed paraneoplastic syndromes either upon diagnosis or during follow-up, 179 age-sex-tumor volume-matched hepatocellular carcinoma patients without paraneoplastic syndromes were selected as controls. Serum liver biochemistry, alpha-fetoprotein, clinical Child-Pugh's score, tumor image studies, histological features, accessibility to treatment, and survival were recorded and compared between patients with and without paraneoplastic syndromes. Prognostic factors in patients' survival were analyzed. The clinical course and survival of hepatocellular carcinoma patients with different paraneoplastic syndromes were also compared. RESULTS: Multivariate Cox regression analysis revealed Child-Pugh's grade C, ineligibility for active treatment, serum alpha-fetoprotein > 10,000 ng/mL, main portal vein tumor thrombosis, and the presence of paraneoplastic syndromes were all independent unfavorable prognostic factors for survival. The median survival from the occurrence of paraneoplastic manifestation to death was only 36 days. Patients with different paraneoplastic syndromes had similar clinical characteristics in Child-Pugh's score, serum alpha-fetoprotein level, tumor volume, prevalence of main portal vein tumor thrombosis, and accessibility for active treatment upon diagnosis. However, erythrocytosis and hypercholesterolemia usually developed earlier in the clinical course, whilst hypoglycemia and hypercalcemia were usually terminal events. Hepatocellular carcinoma patients with erythrocytosis tended to have a longer survival than patients with other paraneoplastic syndromes. CONCLUSIONS: The presence of paraneoplastic syndromes in hepatocellular carcinoma patients is an unfavorable prognostic factor, excluding the occurrence of erythrocytosis.
机译:背景/目的:伴副肿瘤综合征的肝细胞癌患者通常具有较大的肿瘤体积和较高的血清甲胎蛋白。在肝细胞癌患者中是否存在副肿瘤综合征,例如高胆固醇血症,低血糖症,高钙血症和红细胞增多是否是患者生存的重要预后因素,具有临床意义。方法:我们评估了903例肝细胞癌患者副肿瘤综合征的发生率。 179名(20%)患者在诊断或随访期间出现了副肿瘤综合征,选择了179名年龄与性别匹配的无副肿瘤综合征的肝细胞癌患者作为对照。记录并比较有无副肿瘤综合征的患者的血清肝生化,甲胎蛋白,Child-Pugh临床评分,肿瘤影像学,组织学特征,治疗的可及性和生存率。分析了患者生存的预后因素。还比较了具有不同副肿瘤综合征的肝细胞癌患者的临床病程和生存期。结果:多因素Cox回归分析显示,Child-Pugh为C级,不适合接受积极治疗,血清甲胎蛋白> 10,000 ng / mL,主门静脉肿瘤血栓形成和副肿瘤综合征的存在都是独立的不良预后因素。从副肿瘤表现到死亡的中位生存期仅为36天。患有不同副肿瘤综合征的患者在Child-Pugh评分,血清甲胎蛋白水平,肿瘤体积,主要门静脉肿瘤血栓形成的患病率以及诊断后可进行积极治疗的可能性方面具有相似的临床特征。然而,红细胞增多症和高胆固醇血症通常在临床过程中较早发展,而低血糖和高钙血症通常是终末事件。伴有红细胞增多症的肝癌患者往往比其他副肿瘤综合征患者具有更长的生存期。结论:肝细胞癌患者副肿瘤综合征的存在是不利的预后因素,不包括红细胞增多症的发生。

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