Literature DB >> 9636828

Successful treatment with lamivudine for fulminant reactivated hepatitis B infection following intensive therapy for high-grade non-Hodgkin's lymphoma.

F L Clark1, M W Drummond, S Chambers, B A Chapman, W N Patton.   

Abstract

Chronic carriers of Hepatitis B virus (HBV) infection, who are treated for malignant lymphoma, are at high risk of mortality from reactivated HBV infection. We report a case of a 29-year-old male chronic HBV carrier who developed fulminant reactivated HBV infection following intensive chemotherapy for stage IVB large cell B-cell non-Hodgkin's lymphoma associated with extensive central nervous system and bone marrow involvement. Prior to chemotherapy the patient had normal liver function tests and was negative for HBV DNA by semiquantitative PCR assay. Fulminant HBV reactivation was confirmed following clinical deterioration, massive rises in hepatic transaminases (peak alanine aminotransferase = 2,850 U/l), liver biopsy and rising levels of serum HBV DNA. Following treatment with lamivudine 150 mg bd for 18 weeks dramatic and sustained recovery ensued. Symptoms and liver function tests improved within days and HBV DNA became negative within 12 weeks. Our patient later died from relapsed lymphoma but without evidence of reactivated HBV infection. We advise that lamivudine should be considered during intensive chemotherapy treatment of chronic carriers of HBV.

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Year:  1998        PMID: 9636828     DOI: 10.1023/a:1008206519571

Source DB:  PubMed          Journal:  Ann Oncol        ISSN: 0923-7534            Impact factor:   32.976


  9 in total

Review 1.  Lamivudine. A review of its therapeutic potential in chronic hepatitis B.

Authors:  B Jarvis; D Faulds
Journal:  Drugs       Date:  1999-07       Impact factor: 9.546

Review 2.  Prevention of hepatitis B virus reactivation in immunosuppressive therapy or chemotherapy.

Authors:  Waka Ohishi; Kazuaki Chayama
Journal:  Clin Exp Nephrol       Date:  2011-06-01       Impact factor: 2.801

3.  Hepatitis B reactivation after chemotherapy: two decades of clinical research.

Authors:  George K K Lau
Journal:  Hepatol Int       Date:  2008-03-05       Impact factor: 6.047

4.  Reactivation of hepatitis B: pathogenesis and clinical implications.

Authors:  Anthony Post; Shweta Nagendra
Journal:  Curr Infect Dis Rep       Date:  2009-03       Impact factor: 3.725

5.  Preemptive use of lamivudine in breast cancer patients carrying hepatitis B virus undergoing cytotoxic chemotherapy: a longitudinal study.

Authors:  Meng-Shen Dai; Pei-Fen Wu; Jang-Jih Lu; Rong-Yaun Shyu; Tsu-Yi Chao
Journal:  Support Care Cancer       Date:  2004-03       Impact factor: 3.603

6.  Chemotherapy-induced Hepatitis B virus reactivation in HbsAg positive cancer patients: a single center experience.

Authors:  Orhan Onder Eren; Mehmet Artac; Melih Cem Boruban; Ozlem Yavas; Ugur Arslan; Metin Basaranoglu
Journal:  Med Oncol       Date:  2008-11-20       Impact factor: 3.064

7.  Reactivation of hepatitis B virus infection with cytotoxic therapy in non-Hodgkin's lymphoma.

Authors:  M Ozguroglu; A Bilici; H Turna; S Serdengecti
Journal:  Med Oncol       Date:  2004       Impact factor: 3.064

8.  Prophylactic Effect of Lamivudine for Chemotherapy-Induced Hepatitis B Reactivation in Breast Cancer: A Meta-Analysis.

Authors:  Wei Tang; Lun Chen; Ruohui Zheng; Lingxiao Pan; Jin Gao; Xigang Ye; Xiaoshen Zhang; Wenbo Zheng
Journal:  PLoS One       Date:  2015-06-09       Impact factor: 3.240

9.  Alternative therapy and abnormal liver function during adjuvant chemotherapy in breast cancer patients.

Authors:  Jin-Hee Ahn; Sung-Bae Kim; Mi Ra Yun; Jung-Shin Lee; Yoon-Koo Kang; Woo Kun Kim
Journal:  J Korean Med Sci       Date:  2004-06       Impact factor: 2.153

  9 in total

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