Literature DB >> 12514773

A United States compassionate use study of lamivudine treatment in nontransplantation candidates with decompensated hepatitis B virus-related cirrhosis.

Hie-Won L Hann1, Robert J Fontana, Teresa Wright, Gregory Everson, Alfred Baker, Eugene R Schiff, Carolyn Riely, Gaya Anschuetz, Stephen D Gardner, Nathaniel Brown, Dorothea Griffiths.   

Abstract

Patients with hepatitis B-related decompensated cirrhosis have limited treatment options. This prospective, multicenter study assessed lamivudine in 75 patients with decompensated cirrhosis, the majority of whom (93%) were not candidates for liver transplantation. At baseline, all 75 patients tested positive for hepatitis B surface antigen [HBsAg (+)] and 62% tested positive for hepatitis B e antigen [HBeAg (+)]. Hepatitis B virus (HBV) DNA levels were detectable in 64% of patients by the branched chain DNA (bDNA) assay. Patients received lamivudine 100 mg once daily (median duration, 12.7 months; range, 0.5 to 33 months). In patients with detectable HBV DNA pretreatment, the virus became undetectable by the bDNA assay in 69% of patients with > or = 6 months treatment and in 64% overall. Alanine aminotransferase (ALT) level improved in 90% and normalized in 55% of patients with > or = 6 months treatment and in 48% overall. Improvements in bilirubin and albumin levels occurred throughout treatment. The median Child-Pugh score improved from a baseline of 10 to 8 at last visit, with 31% (23/75) having an improved score of > or = 2 points, 57% (43/75) unchanged (< 2 points), and 12% (9/75) worsened (> or = 2 points). A virologic breakthrough developed in eight of 41 patients (18%) after a median of 13.1 months of treatment. Tyrosine-methionine-aspartate-aspartate (YMDD) variant HBV was detected in three of four patients tested. Nevertheless, at last visit, ALT, albumin, and bilirubin levels were similar for patients with and without breakthrough. Lamivudine treatment can lead to significant improvements in liver disease severity in nontransplantation candidates with advanced disease. Additional studies of lamivudine in combination with other antivirals are indicated for the large population of patients worldwide with advanced HBV-related cirrhosis and inadequate access to liver transplantation.

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Year:  2003        PMID: 12514773     DOI: 10.1053/jlts.2003.50005

Source DB:  PubMed          Journal:  Liver Transpl        ISSN: 1527-6465            Impact factor:   5.799


  15 in total

1.  Prevention of post liver transplant HBV recurrence.

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3.  A meta-analysis of nucleos(t)ide analogues in patients with decompensated cirrhosis due to hepatitis B.

Authors:  Yingnan Huang; Hao Wu; Shengdi Wu; Da Fu; Yushui Ma; Xizhong Shen
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Review 4.  Benefits of nucleos(t)ide analog treatments for hepatitis B virus-related cirrhosis.

Authors:  Koichi Honda; Masataka Seike; Kazunari Murakami
Journal:  World J Hepatol       Date:  2015-10-08

5.  YMDD variants of HBV DNA polymerase gene: rapid detection and clinicopathological analysis with long-term lamivudine therapy after liver transplantation.

Authors:  Fei Pei; Jun-Yu Ning; Jiang-Feng You; Jing-Pin Yang; Jie Zheng
Journal:  World J Gastroenterol       Date:  2005-05-14       Impact factor: 5.742

6.  Management of ascites after radical surgery in gastric cancer patients with liver cirrhosis and minimal hepatic dysfunction.

Authors:  Keun Won Ryu; Jun Ho Lee; Young Woo Kim; Joong-Won Park; Jae-Moon Bae
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7.  Fatal liver failure caused by reactivation of lamivudine-resistant hepatitis B virus: a case report.

Authors:  Yuka Suzuki; Hiroshi Yotsuyanagi; Chiaki Okuse; Yoshihiko Nagase; Hideaki Takahashi; Kyoji Moriya; Michihiro Suzuki; Kazuhiko Koike; Shiro Iino; Fumio Itoh
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8.  Adefovir dipivoxil alone or in combination with ongoing lamivudine in patients with decompensated liver disease and lamivudine-resistant hepatitis B virus.

Authors:  Kang Mo Kim; Won-Beom Choi; Young-Suk Lim; Han-Chu Lee; Young-Hwa Chung; Young-Sang Lee; Dong-Jin Suh
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9.  Outcomes of patients with hepatitis B who developed antiviral resistance while on the liver transplant waiting list.

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Journal:  Clin Gastroenterol Hepatol       Date:  2007-10-31       Impact factor: 11.382

10.  Baseline HBV DNA level is the most important factor associated with virologic breakthrough in chronic hepatitis B treated with lamivudine.

Authors:  Hee Bok Chae; Hie-Won Hann
Journal:  World J Gastroenterol       Date:  2007-08-14       Impact factor: 5.742

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