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核苷(酸)类似物在乙型肝炎相关原发性肝癌介入栓塞化疗中的作用*
引用本文:张健珍,张春兰,曾春燕,杨慧勤,孟玉.核苷(酸)类似物在乙型肝炎相关原发性肝癌介入栓塞化疗中的作用*[J].中国肿瘤临床,2016,43(22):1002-1006.
作者姓名:张健珍  张春兰  曾春燕  杨慧勤  孟玉
作者单位:作者单位:广州市第八人民医院感染病科(广州市510060)
基金项目:本文课题受中国肝炎防治基金会王宝恩肝纤维化研究基金项目(编号xjs20121005)资助This work was supported by the Wang Baoen Liver Fibrosis Research Foundation of China Hepatitis Prevention Foundation (xjs20121005)
摘    要:目的:探讨核苷(酸)类似物在乙型肝炎相关原发性肝癌介入栓塞化疗中的作用。方法:回顾性分析广州市第八人民医院2011年1 月至2015年12月诊断收治的乙型肝炎相关原发性肝癌患者174 例,根据病情需要及患者个人意愿分为对照组72例和研究组102 例。对照组采用肝动脉化疗栓塞术(transarterial chemoembolization ,TACE 术)介入治疗。研究组采用TACE 术联合核苷(酸)类似物抗病毒治疗。结果:两组年龄、性别、肿瘤大小及实验室检查等基线资料比较无统计学差异(P > 0.05)。 治疗后研究组和对照组相比,研究组各时点的肝功能均明显改善(P < 0.05);治疗12、24、48W 的AFP 及CAl99水平均较对照组明显降低(P <0.05)。 研究组乙型肝炎病毒DNA (hepatitis B virus DNA ,HBV DNA)不可测率在治疗后4、12、24、48W 分别为13.73% 、33.33% 、50.0% 、76.47% ,对照组分别为11.11% 、16.67% 、22.22% 、25.00% ,研究组治疗12、24、48WHBVDNA不可测率明显高于对照组(P <0.05)。 研究组1 年、3 年生存率分别是96.08% 、90.20%,对照组分别为83.33% 、63.89% ,研究组1、3 年生存率明显高于对照组(P <0.05)。 研究组治疗的显效率、有效率及总有效率均明显高于对照组(P < 0.05)。 结论:肝动脉介入栓塞化疗治疗基础上联合核苷(酸)类似物抗病毒治疗可明显改善乙型肝炎相关原发性肝癌患者 ALT 水平,降低AFP 、CA199 水平,降低HBVDNA 水平,提高HBVDNA 不可测率,保障抗肿瘤治疗的顺利进行,从而提高生存率、延长生存期。有必要开展深入研究,以进—步明确抗病毒治疗在肝癌综合治疗中的作用。 

关 键 词:原发性肝癌    介入栓塞化疗    乙型肝炎病毒    核苷(酸)类似物    抗病毒治疗
收稿时间:2016-08-01

Therapeutic effects of nucleoside analogues (acid) and transarterial chemoemboliza-tion in hepatitis B-related primary liver cancer
Institution:The Eighth People's Hospital of Guangzhou, National Clinical Key Specialty Department of Infectious Diseases, Guangzhou 510060, China
Abstract:Objective:To investigate the therapeutic effects of nucleoside analogues (acid) and transarterial chemoembolization (TACE) on hepatitis B-related primary liver cancer. Methods:Cases from Guangzhou Eighth People's Hospital were retrospectively analyzed between January 2011 and December 2015. A total of 174 patients were diagnosed with hepatitis B-related primary liver cancer. Pa-tients were categorized based on needs and individual goals. The control group included patients who were classified based on needs (n=72), whereas the research group included patients who were classified based on individual goals (n=102). In the control group, 72 patients underwent TACE. In the research group, 102 patients received nucleoside analogue (acid) and TACE. Results:The two groups did not differ significantly in terms of basic clinical parameters, such as age, sex, tumor size, and laboratory examination (P>0.05). After treatment, the research group was compared with the control group. The liver function of patients in the research group significantly improved (P<0.05). AFP and CA199 levels significantly decreased after 12, 24, and 48 weeks of treatment in the research group (P<0.05). The research group had HBVDNA unpredictable rates of 13.73%, 33.33%, 50.0%, and 76.47%after 4, 12, 24, and 48 weeks of treatment, respectively. The control group had HBVDNA unpredictable rates of 11.11%, 16.67%, 22.22%, and 25.00%after 12, 24, and 48 weeks of treatment, respectively. The HBVDNA unpredictable rate was significantly higher in the control group (P<0.05). The treat-ment effects in the research group were better than that of the control group (P<0.05). In the research group, the 1-and 3-year surviv-al rates were 96.08%and 90.20%, respectively. In the control group, the 1-and 3-year survival rates were 83.33%and 63.89%, respec-tively. The difference in survival rates between the two groups was statistically significant (P<0.05). Conclusion:TACE based on com-bined nucleoside analogue (acid) and antiviral treatment improved ALT levels in patients with hepatitis B-related primary liver cancer and decreased AFP, CA199, and HBVDNA levels. Moreover, the HBVDNA unpredictable rate was modified to facilitate the TACE proce-dure, therefore improving the survival rates of patients and prolonging survival. Therefore, the therapeutic actions of antiviral treat-ment on hepatitis B-related primary liver cancer should be further investigated.
Keywords:primary liver cancer  transarterial chemoembolization  hepatitis B virus  nucleoside analogues (acid)  antiviral therapy
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