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发表于 2005-3-19 00:33
Aliment Pharmacol Ther. 2005 Mar 1;21(5):531-7.
Adefovir dipivoxil added to ongoing lamivudine therapy in patients with
lamivudine-resistant hepatitis B e antigen-negative chronic hepatitis B.
Vassiliadis T, Nikolaidis N, Giouleme O, Tziomalos K, Grammatikos N,
Patsiaoura K, Zezos P, Gkisakis D, Theodoropoulos K, Katsinelos P,
Orfanou-Koumerkeridou E, Eugenidis N.
2nd Propaedeutic Department of Internal Medicine, Aristotle University of
Thessaloniki, Hippokration General Hospital, Thessaloniki, Greece.
Summary Background : Long-term treatment with lamivudine is required to
control viral replication in patients with hepatitis B e antigen-negative
chronic hepatitis B, but is associated with a high rate of viral resistance.
The role of adefovir dipivoxil in these patients has not been definitively
evaluated. Aim : To address the role of adefovir in the management of
patients with lamivudine-resistant hepatitis B e antigen-negative chronic
hepatitis B. Methods : Patients were assigned to receive adefovir 10 mg once
daily plus ongoing lamivudine 100 mg once daily for 52 weeks. The primary
end point was reduction in serum hepatitis B virus DNA level (hepatitis B
virus DNA response). Secondary end points included the proportion of
patients with undetectable hepatitis B virus DNA at week 52 (complete
virological response) and the percentage of patients with normalization of
alanine transferase level at week 52 (biochemical response). Results : A
total of 49 consecutive patients were enrolled in this study. After 52 weeks
of treatment, all patients had an hepatitis B virus DNA response and 57.1%
had complete virological response. Biochemical response occurred in 75.6% of
patients. Conclusions : Administration of adefovir in patients with
lamivudine-resistant chronic hepatitis B results in significant suppression
of viral replication. Nevertheless, continuous therapy will probably be
needed in order to maintain remission in these patients.
PMID: 15740536 [PubMed - in process]
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