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Journal of Clinical Oncology, Vol 22, No 5 (March 1), 2004: pp. 927-934
© 2004 American Society of Clinical Oncology.
DOI: 10.1200/JCO.2004.05.161

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Lamivudine for the Prevention of Hepatitis B Virus Reactivation in Hepatitis B s-Antigen Seropositive Cancer Patients Undergoing Cytotoxic Chemotherapy

Winnie Yeo, Paul K.S. Chan, Wing M. Ho, Benny Zee, Kwok C. Lam, Kenny I.K. Lei, Anthony T.C. Chan, Tony S.K. Mok, Jam J. Lee, Thomas W.T. Leung, Sheng Zhong, Philip J. Johnson

From the Department of Clinical Oncology and Department of Microbiology, Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, Hong Kong

Address reprint requests to Winnie Yeo, MD, MRCP, Department of Clinical Oncology, Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, Hong Kong; e-mail: winnieyeo{at}cuhk.edu.hk

PURPOSE: For cancer patients receiving cytotoxic chemotherapy, hepatitis B virus (HBV) reactivation is a well described complication resulting in varying degrees of liver damage. The objectives of this study were to assess the efficacy of the antiviral agent lamivudine in reducing the incidence of HBV reactivation and diminishing morbidity and mortality of cancer patients with chronic HBV infection during chemotherapy.

PATIENTS AND METHODS: Two groups were compared in this nonrandomized study. The prophylactic lamivudine group consisted of 65 patients in a phase II study who were treated with lamivudine before and until 8 weeks after discontinuing chemotherapy. The historical controls consisted of 193 consecutive patients who underwent chemotherapy without prophylactic lamivudine. Significant prognosticators for the development of HBV reactivation were determined based on data from the controls. Potential confounding factors were identified between the two groups. The outcomes were compared.

RESULTS: In the controls, lymphoma and anthracycline usage were factors identified to be associated with reactivation. The two groups were comparable in most baseline characteristics, although in the prophylactic lamivudine group, there were significantly more patients with lymphoma and receiving anthracyclines. In the prophylactic lamivudine group, there was significantly less HBV reactivation (4.6% v 24.4% in the controls; P < .001), fewer incidences of hepatitis (17.5% v 44.6%; P < .0001) that were less severe (4.8% v 18.7%; P = .0005), and less disruption of chemotherapy (15.4% v 34.6%; P = .0029). The reduction in overall mortality was not statistically different.

CONCLUSION: Prophylactic lamivudine significantly reduced the incidence of HBV reactivation and the overall morbidity of cancer patients undergoing chemotherapy.

Supported in part by GlaxoWellcome Ltd, Hong Kong.

Presented in part at the 2002 American Society of Clinical Oncology Annual Meeting, May18-21, 2002, Orlando, FL.

Authors' disclosures of potential conflicts of interest are found at the end of this article.


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