Treatment of lamivudine-resistant chronic hepatitis B infection: a multicenter retrospective study

被引:2
|
作者
Lee, Sun Jae [1 ]
Yim, Hyung Joon [1 ]
Hwang, Seong Gyu [2 ]
Seo, Yeon Seok [1 ]
Kim, Ji Hoon [1 ]
Yoon, Eileen L. [1 ]
Lee, Joong Min [2 ]
Kim, Bo Hyun [3 ]
Park, Sang Jong [3 ]
Park, Young Min [3 ]
Kim, Hong Soo [4 ]
Lee, Se Hwan [4 ]
Ahn, Sang Hoon [5 ]
Lee, Jeong Il [6 ]
Lee, Jin Woo [6 ]
Kim, In Hee [7 ]
Kim, Hyung Soo [8 ]
Hong, Sun Pyo [9 ]
机构
[1] Korea Univ, Coll Med, Div Gastroenterol & Hepatol, Dept Internal Med, Seoul 136705, South Korea
[2] CHA Med Coll, Gyeonggi Do, South Korea
[3] Bundang Jesaeng Hosp, Songnam, South Korea
[4] Soon Chun Hyang Univ, Coll Med, Seoul, South Korea
[5] Yonsei Univ, Coll Med, Seoul, South Korea
[6] Inha Univ, Coll Med, Gyeonggi Do, South Korea
[7] Jeonbuk Natl Univ, Coll Med, Jeonbuk, South Korea
[8] Hallym Univ, Coll Med, Kangdong Sacred Heart Hosp, Seoul, South Korea
[9] GeneMatrix Co, Seoul, South Korea
关键词
adefovir; antiviral resistance; chronic hepatitis B; combination drug therapy; entecavir; lamivudine; multicenter study; RESCUE THERAPY; ENTECAVIR RESISTANCE; ADEFOVIR MONOTHERAPY; COMBINATION THERAPY; VIRUS INFECTION; PLUS ADEFOVIR; RISK; SUBSTITUTIONS; DIPIVOXIL; GENOTYPES;
D O I
10.3109/00365521.2012.722671
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Objectives. To compare the efficacy of rescue therapies in lamivudine (LAM)-resistant chronic hepatitis B (CHB) infections including: (1) adefovir dipivoxil (ADV) monotherapy, (2) ADV plus LAM combination therapy and (3) entecavir (ETV) 1.0 mg monotherapy. Materials and methods. The authors designed a multicenter-retrospective study. Eight institutions participated in the study from Korea. Results. A total of 343 LAM-resistant CHB patients were enrolled. The proportion of patients with undetectable serum hepatitis B virus (HBV) DNA levels at month 24 after the initiation of rescue therapy was higher in the ADV plus LAM combination therapy group (39/64, 60.9%) than in the ADV monotherapy (50/126, 39.7%) and ETV 1.0 mg monotherapy (19/48, 39.6%) groups (p = 0.014). Mean serum HBV DNA levels at 24 months were 2.07 +/- 1.21 log(10) IU/ml in the ADV plus LAM combination therapy group, 2.74 +/- 1.74 log(10) IU/ml in the ADV monotherapy group and 3.08 +/- 1.97 log(10) IU/ml in the ETV 1.0 mg monotherapy group (p = 0.014). In multivariate analysis, a finding of undetectable serum HBV DNA level at 6 months and ADV plus LAM combination therapy (vs. ADV) was an independent factor for predicting undetectable serum HBV DNA at month 24 (odds ratio, 1.003; 95% confidence interval, 1.000-1.006; p = 0.026). Conclusions. ADV plus LAM combination therapy is more effective in reducing viral load than switching to ADV or ETV 1.0 mg in patients with LAM-resistant CHB.
引用
收藏
页码:196 / 204
页数:9
相关论文
共 50 条
  • [31] Clinical course after stopping lamivudine in chronic hepatitis B patients with lamivudine-resistant mutants
    Wong, VWS
    Chan, HLY
    Wong, ML
    Tam, JSL
    Leung, NWY
    ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2004, 19 (03) : 323 - 329
  • [32] Predictors of virologic response and resistance to adefovir in patients with lamivudine-resistant chronic hepatitis B virus infection
    Park, Neung Hwa
    Shin, Jung Woo
    Park, Jin Woo
    Jung, Seok Won
    Jeong, In Du
    Bang, Sung-Jo
    Kim, Do Ha
    HEPATOLOGY, 2007, 46 (04) : 675A - 676A
  • [33] The real danger of lamivudine-resistant hepatitis B virus infection in the immunocompromised host
    Vargas, HE
    LIVER TRANSPLANTATION, 2001, 7 (03) : 279 - 281
  • [34] Treatment with adefovir alone or in combination with lamivudine in chronic hepatitis B lamivudine-resistant patients: Results after two years
    Barbon, V.
    Marzano, A.
    Carenzi, S.
    Lagget, M.
    Alessandria, C.
    Olivero, A.
    Gaia, S.
    Ciancio, A.
    Smedile, A.
    Rizzetto, M.
    JOURNAL OF HEPATOLOGY, 2006, 44 : S178 - S179
  • [35] Tenofovir Monotherapy versus Tenofovir plus Lamivudine or Telbivudine Combination Therapy in Treatment of Lamivudine-Resistant Chronic Hepatitis B
    Lee, Yun Bin
    Jung, Eun Uk
    Kim, Bo Hyun
    Lee, Jeong-Hoon
    Cho, Hyeki
    Ahn, Hongkeun
    Choi, Won-Mook
    Cho, Young Youn
    Lee, Minjong
    Yoo, Jeong-Ju
    Cho, Yuri
    Lee, Dong Hyeon
    Cho, Eun Ju
    Yu, Su Jong
    Park, Sung Jae
    Kim, Yoon Jun
    Park, Joong-Won
    Lee, Youn Jae
    Kim, Chang-Min
    Yoon, Jung-Hwan
    Kim, Chung Yong
    Lee, Hyo-Suk
    ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2015, 59 (02) : 972 - 978
  • [36] Clinical and virological effects during two years of ongoing adefovir dipivoxil in the treatment of lamivudine-resistant chronic hepatitis B infection
    Gornals, JB
    Casanovas, T
    Sabidó, M
    Baliellas, C
    Casanovas, A
    Cañas, C
    Serrano, T
    Verdura, B
    Chahri, N
    Gil-Vernet, S
    Figueras, J
    TRANSPLANTATION PROCEEDINGS, 2005, 37 (09) : 3957 - 3959
  • [37] Ganciclovir treatment of lamivudine-resistant HBV infection
    Bozkaya, H
    Yurdaydin, C
    Karayalcin, S
    Cinar, K
    Bozdayi, M
    Uzunalimoglu, O
    JOURNAL OF HEPATOLOGY, 2002, 36 : 229 - 230
  • [38] Strategy for lamivudine-resistant YMDD mutant-associated chronic hepatitis B
    Kiyosawa, K
    Tanaka, E
    JOURNAL OF GASTROENTEROLOGY, 2001, 36 (02) : 139 - 141
  • [39] Adefovir dipivoxil resistance patterns in patients with lamivudine-resistant chronic hepatitis B
    Santantonio, Teresa
    Fasano, Massimo
    Durantel, Sandra
    Barraud, Luc
    Heichen, Manuela
    Guastadisegni, Angela
    Pastore, Giuseppe
    Zoulim, Fabien
    ANTIVIRAL THERAPY, 2009, 14 (04) : 557 - 565
  • [40] Resistance to adefovir dipivoxil in patients with lamivudine-resistant chronic hepatitis B.
    Osiowy, C
    Heathcote, J
    Zoulim, F
    Willems, B
    Villeneuve, JP
    HEPATOLOGY, 2005, 42 (04) : 586A - 587A