The prophylactic use of lamivudine can maintain dose-intensity of adriamycin in hepatitis-B surface antigen (HBs Ag)-positive patients with Non-Hodgkin's lymphoma who receive cytotoxic chemotherapy

• Published in: Journal of Korean medical science Vol. 18; no. 6; pp. 849 - 854
• Main Authors: Lee, Gyeong-Won, Ryu, Min-Hee, Lee, Jae-Lyun, Oh, Sukjoong, Kim, Eunkyoung, Lee, Jae-Hwan, Kim, Seung-Bae, Kim, Sang-We, Suh, Cheolwon, Lee, Kyoo-Hyung, Kim, Woo-Kun, Lee, Jung-Shin, Kang, Yoon-Koo
• Format: Journal Article
• Language: English
• Published: Korea (South) Korean Academy of Medical Sciences 01.12.2003
• Subjects: Adult; Aged; Antibiotics, Antineoplastic - therapeutic use; Doxorubicin - therapeutic use; Female; Hepatitis B - complications; Hepatitis B - diagnosis; Hepatitis B - drug therapy; Hepatitis B Surface Antigens - analysis; Hepatitis B virus - metabolism; Humans; Lamivudine - therapeutic use; Lymphoma, Non-Hodgkin - complications; Lymphoma, Non-Hodgkin - drug therapy; Lymphoma, Non-Hodgkin - metabolism; Male; Middle Aged; Reverse Transcriptase Inhibitors - therapeutic use; Survival Rate; Virus Activation
• ISSN: 1011-8934; 1598-6357
• DOI: 10.3346/jkms.2003.18.6.849

We investigated the effectiveness of lamivudine to prevent hepatitis flare up due to reactivation of hepatitis-B virus (HBV) in hepatitis-B surface antigen (HBsAg)-positive patients with Non-Hodgkin's lymphoma (NHL) during cytotoxic chemotherapy. HBsAg-positive patients with NHL were identified from the lymphoma database of the Asan Medical Center from January 1995 to August 2002, and their medical records were reviewed. We found that 31 patients were received cytotoxic chemotherapy among 41 NHL patients with HBsAg-positive during same period. We divided them into 2 groups of HBsAg patients with NHL as follows: Group A who received cytotoxic chemotherapy with lamivudine 100 mg daily; Group B without any prophylactic antiviral therapy. There were no significant differences between Group A and B in several clinical variables. Seventeen patients (85%) in group B and one patient (9%) in Group A had hepatitis due to reactivation of HBV (p<0.001), with one hepatic failure related death in Group B and none in group A. The mean dose intensity of adriamycin actually delivered was 13.3 mg/m2/week (80% Relative Dose intensity (RDI)) in Group A and 9.1 mg/m2/week (55% RDI) in Groups B (p<0.001). Our data suggest that the frequency of chemotherapy-related HBV reactivation may be significantly decreased by lamivudine prophylaxis with maintenance of the dosage of adriamycin.