Department of Health Promotion, Section of Gastroenterology and Hepatology, Mother and Child Care, Internal Medicine and Medical Specialties, PROMISE, University of Palermo, Palermo, Italy.
Department of Surgery & Cancer, Imperial College London, London, UK.
Liver Int. 2024 Nov;44(11):2890-2903. doi: 10.1111/liv.16064. Epub 2024 Aug 29.
Patients with overt or occult hepatitis B virus (HBV) infection receiving immunosuppressive treatments have a wide risk of HBV reactivation (HBVr). We performed meta-analysis with decision curve analyses (DCA) to estimate the risk of HBVr in HBsAg-negative anti-HBc-positive patients naïve to nucleos(t)ide analogues (NAs) receiving immunosuppressive treatments.
Studies were identified through literature search until October 2022. Pooled estimates were obtained using random-effects model. Subgroup analyses were performed according to underlying disease and immunosuppressive treatments. DCA was used to identify the threshold probability associated with the net benefit of antiviral prophylaxis in HBsAg-negative anti-HBc-positive patients. We selected 68 studies (40 retrospective and 28 prospective), including 8034 patients with HBsAg negative anti-HBc positive. HBVr was 4% (95% CI 3%-6%) in HBsAg-negative anti-HBc-positive patients, with a significantly high heterogeneity (I 69%; p < .01). The number-needed-to-treat (NNT) by DCA ranged from 8 to 24 for chemotherapy plus rituximab, from 12 to 24 for targeted therapies in cancer patients and from 13 to 39 for immune-mediated diseases. Net benefit was small for monoclonal antibodies.
Our DCA in HBsAg-negative anti-HBc-positive patients provided evidence that NA prophylaxis is strongly recommended in patients treated with chemotherapy combined with rituximab and could be appropriate in patients with cancer treated with targeted therapies and in patients with immune-mediated diseases. Finally, in patients with cancer treated with monoclonal antibodies or with chemotherapy without rituximab, the net benefit is even lower.
接受免疫抑制治疗的显性或隐匿性乙型肝炎病毒(HBV)感染患者有广泛的 HBV 再激活(HBVr)风险。我们进行了荟萃分析和决策曲线分析(DCA),以评估 HBsAg 阴性抗-HBc 阳性、初治核苷(酸)类似物(NAs)的免疫抑制治疗患者的 HBVr 风险。
通过文献检索直到 2022 年 10 月确定了研究。使用随机效应模型获得汇总估计值。根据基础疾病和免疫抑制治疗进行亚组分析。DCA 用于确定与 HBsAg 阴性抗-HBc 阳性患者抗病毒预防净获益相关的阈值概率。我们选择了 68 项研究(40 项回顾性和 28 项前瞻性),共纳入 8034 例 HBsAg 阴性抗-HBc 阳性患者。HBVr 在 HBsAg 阴性抗-HBc 阳性患者中为 4%(95%CI 3%-6%),异质性显著较高(I 69%;p<.01)。DCA 的需要治疗人数(NNT)范围为化疗加利妥昔单抗为 8-24,癌症患者的靶向治疗为 12-24,免疫介导性疾病为 13-39。单克隆抗体的净获益较小。
我们在 HBsAg 阴性抗-HBc 阳性患者中的 DCA 提供了证据,表明 NA 预防强烈推荐用于接受化疗联合利妥昔单抗治疗的患者,对于接受靶向治疗的癌症患者和免疫介导性疾病患者可能是合适的。最后,对于接受单克隆抗体治疗或无利妥昔单抗化疗的癌症患者,净获益甚至更低。