Leaw Shiang Jiin, Yen Chia Jui, Huang Wen Tsung, Chen Tsai Yun, Su Wu Chou, Tsao Chao Jung
Department of Internal Medicine, National Cheng-Kung University Hospital Tainan, 138 Sheng Li Road, 70428, Tainan, Taiwan ROC.
Ann Hematol. 2004 May;83(5):270-5. doi: 10.1007/s00277-003-0825-8. Epub 2003 Dec 5.
The hepatitis B virus (HBV) reactivation rate among hepatitis B virus surface antigen (HBsAg)-positive patients undergoing chemotherapy ranges from 21 to 35% with a mortality rate of 4-41%. The risk is significantly evident in patients with aggressive lymphoma, which is highly responsive to standard chemotherapy with cyclophosphamide, hydroxydaunomycin, vincristine, and prednisone (CHOP) achieving a complete response rate of 60-80% and 5-year survival rate of 30-50% with only 1% of treatment-related mortality. Alpha-Interferon and lamivudine were given as preemptive treatment for HBV reactivation in HBsAg-positive patients treated for aggressive lymphoma consecutively from 1994 to 1997 and 1998 to 2001, respectively, in our institution. The outcome of 77 HBsAg-positive patients treated for aggressive lymphoma at our institution from 1990 to 2001 was studied. Of these patients, 53 did not receive prophylaxis while 13 received subcutaneous alpha-interferon 3 x 10(6) U thrice weekly and 11 received oral lamivudine 100 mg/day simultaneously with chemotherapy. Seventeen patients in the non-prophylactic group experienced HBV reactivation (32%), seven of whom progressed to fatal fulminant hepatitis (41%), which is associated with 13.2% of the mortality rate among the non-prophylactic patients. None of the 24 patients in the prophylactic group had grade III or IV toxicity or elevated ALT level greater than fivefold exceeding 200 IU/l suggestive of clinical hepatitis that required dose reduction or delayed chemotherapy. Thus, preemptive use of alpha-interferon or lamivudine in HBsAg-positive lymphoma patients undergoing chemotherapy may be a promising approach to prevent HBV reactivation that carries a risk of delayed treatment or even fatal outcome.
接受化疗的乙肝表面抗原(HBsAg)阳性患者中,乙肝病毒(HBV)再激活率为21%至35%,死亡率为4%至41%。侵袭性淋巴瘤患者的这种风险尤为显著,侵袭性淋巴瘤对环磷酰胺、羟基柔红霉素、长春新碱和泼尼松(CHOP)标准化疗反应良好,完全缓解率为60%至80%,5年生存率为30%至50%,治疗相关死亡率仅为1%。1994年至1997年以及1998年至2001年,我院分别对接受侵袭性淋巴瘤治疗的HBsAg阳性患者给予α干扰素和拉米夫定作为HBV再激活的预防性治疗。我们研究了1990年至2001年在我院接受侵袭性淋巴瘤治疗的77例HBsAg阳性患者的结局。这些患者中,53例未接受预防治疗,13例接受皮下注射α干扰素3×10⁶U,每周三次,11例在化疗同时接受口服拉米夫定100mg/天。未预防组的17例患者发生了HBV再激活(32%),其中7例进展为致命性暴发性肝炎(41%),这与未预防组患者13.2%的死亡率相关。预防组的24例患者均无III级或IV级毒性反应,或谷丙转氨酶(ALT)水平升高超过五倍(超过200IU/L)提示临床肝炎,需要减少剂量或延迟化疗。因此,对接受化疗的HBsAg阳性淋巴瘤患者预防性使用α干扰素或拉米夫定可能是预防HBV再激活的一种有前景的方法,HBV再激活有导致治疗延迟甚至致命结局的风险。