臨牀消化器内科 Vol.19 No.11(1-6)


特集名 B型肝炎 update 2004
題名 B型肝炎の病態update (6) 肝細胞癌に対する肝動注化学療法時にみられるB型肝炎の急性増悪とその予防
発刊年月 2004年 10月
著者 鳥村 拓司 久留米大学医学部第二内科
著者 永松 洋明 久留米大学医学部第二内科
著者 板野 哲 久留米大学医学部第二内科
著者 松垣 諭 久留米大学医学部第二内科
著者 神代 龍吉 久留米大学医学部第二内科
著者 佐田 通夫 久留米大学医学部第二内科
【 要旨 】 HBs抗原陽性担癌患者の化学療法に起因するB型肝炎の急性増悪は重篤な合併症である.HBVに起因する肝細胞癌に肝動注化学療法を施行した症例を解析した結果,HBe抗原陽性の8例すべてで急性増悪が認められ,うち3例が肝不全で死亡していた.単変量と多変量解析の結果,HBe抗原陽性が急性増悪の関連因子であることが判明した.しかし,ラミブジンを予防投与し肝動注化学療法を施行したHBe抗原陽性の肝細胞癌患者では,HBV DNA値は減少し急性増悪は1例も認められなかった.以上より,ラミブジンでHBVの増殖を抑制することで,HBe抗原陽性の肝細胞癌患者も安全に肝動注化学療法が施行できることが明らかとなった.
Theme Hepatitis B Update 2004
Title Prophylactic Lamivudine Administration Prevents Exacerbation of HBV Related Liver Damage in Patients with Hepatocellular Carcinoma Undergoing Transhepatic Arterial Infusion Chemotherapy
Author Takuji Torimura Second Department of Medicine, Kurume University School of Medicine
Author Hiroaki Nagamatsu Second Department of Medicine, Kurume University School of Medicine
Author Satoshi Itano Second Department of Medicine, Kurume University School of Medicine
Author Satoru Matsugaki Second Department of Medicine, Kurume University School of Medicine
Author Ryukichi Kumashiro Second Department of Medicine, Kurume University School of Medicine
Author Michio Sata Second Department of Medicine, Kurume University School of Medicine
[ Summary ] A flare up of hepatitis, due to the reactivation of hepatitis B virus (HBV), is a serious complication in patients with malignant diseases receiving chemotherapy. In thirty three patients with HBV-related hepato cellular carcinoma (HCC) who received trans-hepatic arterial chemotherapy, all of the eight patients who were HBe antigen positive were found to have exacerbated liver damage. Of these, three patients died of liver failure. The only associated factor for the excerbation of liver damage was HBe antigen positivity. From the year 2000, prophylactic lamivudine administration was performed on eight patients who were HBe antigen positive HCC prior to trans-hepatic arterial chemotherapy. None of the eight patients who received Lamivudine administration showed exacerbation of liver damage. Lamivudine administration significantly reduced HBV-DNA levels prior to chemotherapy (base line ; 6.6+-1.0 LGE/ml, prior to chemotherapy; 4.7+-1.0 LGE/ml). AST and ALT levels in the lamivudine-treated group did not change throughout chemotherapy. Total bilirubin and prothrombin time levels also did not show any significant change throughout chemotherapy. 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 HCC.
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