Department of Dermatology, Hospital Universitario de la Princesa, Madrid, Spain.
Br J Dermatol. 2013 Mar;168(3):609-16. doi: 10.1111/bjd.12045.
Both the safety and efficacy of biologic therapy may be affected in the presence of highly prevalent chronic viral hepatitis.
To evaluate the safety and effectiveness of ustekinumab and antitumour necrosis factor therapy in patients with psoriasis and concomitant chronic viral hepatitis.
This was a retrospective, multicentre study. Twenty-five patients with psoriasis and concurrent hepatitis C virus (HCV) (20 patients) or hepatitis B virus (HBV) (five patients) infection who had received at least one biologic agent (etanercept, 21 treatments; adalimumab, four; ustekinumab, four; infliximab, two) were included. Clinical, imaging and laboratory data were recorded.
In the case of HCV infection, the majority of the patients did not exhibit increases in their viral load or serum liver tests. Aspartate aminotransferase, alanine aminotransferase and gamma glutamyl transpeptidase were doubled from the baseline measurement in only one patient treated with etanercept. Two other cases exhibited viral load increases during the follow-up period. In total, 18 of the 26 treatments achieved a 75% improvement in their Psoriasis Area and Severity Index (PASI 75) score during the follow-up period. Two patients treated with etanercept were diagnosed with hepatocellular carcinoma. In the case of HBV infection, all of the patients were being treated with antiviral therapy, and none presented significant variations in viral load or serum liver enzymes. All patients achieved a PASI 75 during follow-up.
Biologic therapy was effective and safe for the majority of our patients with HCV and HBV infection, although there may be a risk of reactivation or aggravation. We describe the first cases to receive ustekinumab. The use of biologics should be limited to those cases in which the risk-benefit ratio is justified.
在慢性病毒性肝炎高发的情况下,生物疗法的安全性和疗效都可能受到影响。
评估银屑病合并慢性病毒性肝炎患者使用乌司奴单抗和抗肿瘤坏死因子治疗的安全性和有效性。
这是一项回顾性、多中心研究。纳入了 25 例银屑病合并丙型肝炎病毒(HCV)(20 例)或乙型肝炎病毒(HBV)(5 例)感染的患者,这些患者至少接受过一种生物制剂(依那西普,21 次治疗;阿达木单抗,4 次;乌司奴单抗,4 次;英夫利昔单抗,2 次)。记录了临床、影像学和实验室数据。
在 HCV 感染的情况下,大多数患者的病毒载量或血清肝酶均未升高。仅 1 例接受依那西普治疗的患者天门冬氨酸氨基转移酶、丙氨酸氨基转移酶和γ-谷氨酰转肽酶从基线测量值翻倍。另外 2 例在随访期间出现病毒载量增加。在随访期间,26 次治疗中有 18 次达到了银屑病面积和严重程度指数(PASI75)改善 75%。2 例接受依那西普治疗的患者被诊断为肝细胞癌。在 HBV 感染的情况下,所有患者均接受抗病毒治疗,病毒载量或血清肝酶均无明显变化。所有患者在随访期间均达到了 PASI75。
对于大多数 HCV 和 HBV 感染的患者,生物疗法是有效且安全的,但可能存在再激活或加重的风险。我们描述了首例接受乌司奴单抗治疗的患者。生物制剂的使用应仅限于风险效益比合理的病例。