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预防性给予拉米夫定可预防接受经肝动脉灌注化疗的HBe抗原阳性肝细胞癌患者肝损伤的加重。

Prophylactic lamivudine administration prevents exacerbation of liver damage in HBe antigen positive patients with hepatocellular carcinoma undergoing transhepatic arterial infusion chemotherapy.

作者信息

Nagamatsu Hiroaki, Itano Satoshi, Nagaoka Sakae, Akiyoshi Junji, Matsugaki Satoru, Kurogi Junichi, Tajiri Nobuyoshi, Yamasaki Sanki, Koga Hironori, Torimura Takuji, Kumashiro Ryukichi, Sata Michio

机构信息

Second Department of Medicine, Kurume University School of Medicine, 830-0011 Kurume, Japan.

出版信息

Am J Gastroenterol. 2004 Dec;99(12):2369-75. doi: 10.1111/j.1572-0241.2004.40069.x.

Abstract

BACKGROUND AND AIMS

Exacerbation of liver damage during transhepatic arterial infusion chemotherapy (THAIC) is a critical complication in patients with hepatitis B virus (HBV) related hepatocellular carcinoma (HCC). We previously reported that HBe antigen positivity was the associating factor for the exacerbation of liver damage. In the present study, we investigated the effect of lamivudine administration for exacerbation of liver damage in such patients.

PATIENTS AND METHODS

Seventeen patients with HBV-related hepatocellular carcinoma who received THAIC were reviewed. Eight of these patients received lamivudine administration. Nine patients did not receive lamivudine administration. All patients were HBe antigen positive. Liver function tests, liver enzymes, HBV-DNA levels, HBe antigen, HBe antibody, and mutation in the precore and core-promoter regions of HBV DNA were evaluated.

RESULTS

In the lamivudine-treated group, HBV-DNA levels were significantly reduced and did not increase throughout chemotherapy. Lamivudine did not induce any changes in precore or core-promoter regions. Although levels of alanine aminotransferase (ALT), asparate aminotransferase (AST), total bilirubin, and prothrombin time (PT) in the lamivudine-treated group did not change, levels of ALT, AST and total bilirubin increased, and PT were prolonged in the untreated group by chemotherapy. No patients receiving lamivudine administration showed exacerbation of liver damage. Exacerbation of liver damage was detected in six patients without lamivudine administration. Of these, three patients died of progressive liver failure due to reactivation of HBV.

CONCLUSION

These results indicate that prophylactic lamivudine administration reduces HBV-DNA levels and prevents exacerbation of liver damage throughout the period of chemotherapy in HBe antigen positive patients with hepatocellular carcinoma.

摘要

背景与目的

经肝动脉灌注化疗(THAIC)期间肝损伤加重是乙型肝炎病毒(HBV)相关肝细胞癌(HCC)患者的一种关键并发症。我们之前报道HBe抗原阳性是肝损伤加重的相关因素。在本研究中,我们调查了拉米夫定给药对这类患者肝损伤加重的影响。

患者与方法

回顾了17例接受THAIC的HBV相关肝细胞癌患者。其中8例患者接受了拉米夫定给药。9例患者未接受拉米夫定给药。所有患者HBe抗原均为阳性。评估了肝功能检查、肝酶、HBV-DNA水平、HBe抗原、HBe抗体以及HBV DNA前核心区和核心启动子区的突变情况。

结果

在拉米夫定治疗组中,HBV-DNA水平显著降低,且在整个化疗过程中未升高。拉米夫定未诱导前核心区或核心启动子区发生任何变化。虽然拉米夫定治疗组的丙氨酸氨基转移酶(ALT)、天冬氨酸氨基转移酶(AST)、总胆红素和凝血酶原时间(PT)水平未改变,但未治疗组的ALT、AST和总胆红素水平在化疗后升高,PT延长。接受拉米夫定给药的患者均未出现肝损伤加重。未接受拉米夫定给药的6例患者中检测到肝损伤加重。其中,3例患者因HBV再激活死于进行性肝衰竭。

结论

这些结果表明,预防性给予拉米夫定可降低HBe抗原阳性肝细胞癌患者化疗期间的HBV-DNA水平,并预防肝损伤加重。

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