2003The Korean Journal of Internal MedicineOpen access

A comparative study on the efficacy between interferon alpha monotherapy and lamivudine-interferon combination therapy in chronic hepatitis B patients

Tae-Hyung Lim, D. Jeong, Sang Lee, Seung‐Ho Han, Sukhwan Chung, Dong-Sung Kum, Hee-Rin Joo, Jin-Seok Jang, Jong‐Hoon Lee, Myoung-Hwan Rho, Sang‐Young Han, Seok-Ryeol Choi, Woo-Won Shin

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Abstract

Background : At present, lamivudine-interferon combination therapy is being tried on chronic hepatitis B patients who had no significant response to interferon-alpha mono-therapy. The therapeutic effect of lamivudine-interferon combination therapy is showing various outcomes depending on the period of therapy and the status of the patient. Thus we conducted this study to compare the therapeutic effect of lamivudine-interferon combination therapy versus interferon-alpha monotherapy in korean patients with chronic hepatitis B. Method : Among the chronic hepatitis B patients, 138 patients who showed positive to HBeAg, and serum HBV DNA levels are over 5 pg/mL and serum ALT levels are over 40 IU/L were allocated to IFN- monotherapy group (70 patients) and lamivudine-interferon combination therapy group (66 patients). We compared two groups on ALT normalization rate, HBeAg seroconversion rate, HBV DNA loss rate and HBeAg loss rate in both group. IFN- was percutaneously injected three times a week. Mean administered dose was 27125 (B11841) MU and mean administered duration was 6.4 (1.6) months. Lamivudine was concomitantly and continuously administered with IFN- for over 6 months (mean 13.2/16.5). The lamivudine therapy was terminated at the point when HBeAg turned positive into negative. Results : Mean follow-up period was 28 months. HBeAg loss rate was 40.9% in lamivudineinterferon combination therapy group and 28.6% in IFN- monotherapy group on the 12th month of the therapy, showing there was no significant difference between the two groups (p=0.13). HBeAg seroconversion rate was 40.9% in lamivudine-interferon combination therapy group and 21.4% in IFN- monotherapy group on the 12th month of the therapy (p=0.014). HBV DNA loss rate was 90.9% in lamivudine-interferon combination therapy group and 88.6% in IFN- monotherapy group within 12months of the therapy, showing there was no significant difference between the two groups (p=0.35). Serum ALT normalization rate was 92.4% in lamivudine-interferon combination therapy group and 85.7% in IFN- monotherapy group within 12months of the therapy, showing there was no significant difference between the two groups (p=0.11). Conclusion : The lamivudine-interferon combination therapy compared to the Interferon-alpha monotherapy showed a statistically significant higher HBeAg seroconversion rate.

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Background : At present, lamivudine-interferon combination therapy is being tried on chronic hepatitis B patients who had no significant response to interferon-alpha mono-therapy. The therapeutic effect of lamivudine-interferon combination therapy is showing various outcomes depending on the period of therapy and the status of the patient. Thus we conducted this study to compare the therapeutic effect of lamivudine-interferon combination therapy versus interferon-alpha monotherapy in korean patients with chronic hepatitis B. Method : Among the chronic hepatitis B patients, 138 patients who showed positive to HBeAg, and serum HBV DNA levels are over 5 pg/mL and serum ALT levels are over 40 IU/L were allocated to IFN- monotherapy group (70 patients) and lamivudine-interferon combination therapy group (66 patients). We compared two groups on ALT normalization rate, HBeAg seroconversion rate, HBV DNA loss rate and HBeAg loss rate in both group. IFN- was percutaneously injected three times a week. Mean administered dose was 27125 (B11841) MU and mean administered duration was 6.4 (1.6) months. Lamivudine was concomitantly and continuously administered with IFN- for over 6 months (mean 13.2/16.5). The lamivudine therapy was terminated at the point when HBeAg turned positive into negative. Results : Mean follow-up period was 28 months. HBeAg loss rate was 40.9% in lamivudineinterferon combination therapy group and 28.6% in IFN- monotherapy group on the 12th month of the therapy, showing there was no significant difference between the two groups (p=0.13). HBeAg seroconversion rate was 40.9% in lamivudine-interferon combination therapy group and 21.4% in IFN- monotherapy group on the 12th month of the therapy (p=0.014). HBV DNA loss rate was 90.9% in lamivudine-interferon combination therapy group and 88.6% in IFN- monotherapy group within 12months of the therapy, showing there was no significant difference between the two groups (p=0.35). Serum ALT normalization rate was 92.4% in lamivudine-interferon combination therapy group and 85.7% in IFN- monotherapy group within 12months of the therapy, showing there was no significant difference between the two groups (p=0.11). Conclusion : The lamivudine-interferon combination therapy compared to the Interferon-alpha monotherapy showed a statistically significant higher HBeAg seroconversion rate.

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Available abstract

Background : At present, lamivudine-interferon combination therapy is being tried on chronic hepatitis B patients who had no significant response to interferon-alpha mono-therapy. The therapeutic effect of lamivudine-interferon combination therapy is showing various outcomes depending on the period of therapy and the status of the patient. Thus we conducted this study to compare the therapeutic effect of lamivudine-interferon combination therapy versus interferon-alpha monotherapy in korean patients with chronic hepatitis B. Method : Among the chronic hepatitis B patients, 138 patients who showed positive to HBeAg, and serum HBV DNA levels are over 5 pg/mL and serum ALT levels are over 40 IU/L were allocated to IFN- monotherapy group (70 patients) and lamivudine-interferon combination therapy group (66 patients). We compared two groups on ALT normalization rate, HBeAg seroconversion rate, HBV DNA loss rate and HBeAg loss rate in both group. IFN- was percutaneously injected three times a week. Mean administered dose was 27125 (B11841) MU and mean administered duration was 6.4 (1.6) months. Lamivudine was concomitantly and continuously administered with IFN- for over 6 months (mean 13.2/16.5). The lamivudine therapy was terminated at the point when HBeAg turned positive into negative. Results : Mean follow-up period was 28 months. HBeAg loss rate was 40.9% in lamivudineinterferon combination therapy group and 28.6% in IFN- monotherapy group on the 12th month of the therapy, showing there was no significant difference between the two groups (p=0.13). HBeAg seroconversion rate was 40.9% in lamivudine-interferon combination therapy group and 21.4% in IFN- monotherapy group on the 12th month of the therapy (p=0.014). HBV DNA loss rate was 90.9% in lamivudine-interferon combination therapy group and 88.6% in IFN- monotherapy group within 12months of the therapy, showing there was no significant difference between the two groups (p=0.35). Serum ALT normalization rate was 92.4% in lamivudine-interferon combination therapy group and 85.7% in IFN- monotherapy group within 12months of the therapy, showing there was no significant difference between the two groups (p=0.11). Conclusion : The lamivudine-interferon combination therapy compared to the Interferon-alpha monotherapy showed a statistically significant higher HBeAg seroconversion rate.

Key concepts: Lamivudine, Medicine, Combination therapy, HBeAg, Gastroenterology, Internal medicine, Seroconversion, Alpha interferon

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