Lv Yan-Qing, Guo Ru-Hua, Liu Kun-Yu, Li Jia-Jie, Ji Hui-Fan
Department of Hepatobiliary and Pancreatic Medicine, The First Hospital of Jilin University Changchun, Changchun, Jilin, China.
Front Med (Lausanne). 2025 Jan 9;11:1483744. doi: 10.3389/fmed.2024.1483744. eCollection 2024.
Sequential or combined treatment with nucleos(t)ide analogs (NAs) and pegylated interferon alpha-2b (Peg-IFN--2b) can improve the clinical cure rate. However, its clinical application is limited due to the adverse reactions associated with IFN.
A multi-center prospective observational study was conducted involving 59 NAs-treated chronic hepatitis B (CHB) patients who were treated with a combination therapy of NAs and Peg-IFN--2b for 48 weeks. Another 327 NAs-treated patients received NAs monotherapy for 48 weeks. At the end of the treatment, patients were classified into either the clinically cured group or the non-clinically cured group based on clinical efficacy. The study aimed to analyze the clinical cure rate and the predictive factors.
After propensity score matching (PSM), a total of 104 patients were included in the exposure and the control groups. After 48 weeks of treatment, 13 patients in the exposed group achieved clinical cure, with a cure rate of 25%. In contrast, in the control group was 1.92%. The clinical cure rate was greater in the population with CHB or compensated cirrhosis treated with sequential or combined Peg-IFN--2b and NAs than in the control group ( < 0.001). Patients treated with Peg-IFN-α-2b were divided into a clinical cure group and a non-clinical cure group for single-factor regression and multi-factor binary logistic regression. The results showed that baseline qHBsAg [relative ratio (RR) = 0.997, 95%CI: [0.995, 0.999], = 0.031] and △TBiL (RR = 0.698, 95%CI: [0.555, 0.879], = 0.002) were independent influencing factors for achieving clinical cure in patients with CHB or compensated cirrhosis.
A lower baseline qHBsAg and decrease in TBiL at 24 weeks of treatment are independent influencing factors for achieving clinical cure. The lower the baseline qHBsAg and the higher the △TBiL levels after 24 weeks of treatment, the higher the probability of patients achieving clinical cure.
核苷(酸)类似物(NAs)与聚乙二醇化干扰素α-2b(Peg-IFN-α-2b)序贯或联合治疗可提高临床治愈率。然而,由于与干扰素相关的不良反应,其临床应用受到限制。
进行了一项多中心前瞻性观察性研究,纳入59例接受NAs治疗的慢性乙型肝炎(CHB)患者,给予NAs与Peg-IFN-α-2b联合治疗48周。另外327例接受NAs治疗的患者接受NAs单药治疗48周。治疗结束时,根据临床疗效将患者分为临床治愈组和非临床治愈组。该研究旨在分析临床治愈率及预测因素。
经过倾向评分匹配(PSM)后,暴露组和对照组共纳入104例患者。治疗48周后,暴露组13例患者实现临床治愈,治愈率为25%。相比之下,对照组为1.92%。接受序贯或联合Peg-IFN-α-2b和NAs治疗的CHB或代偿期肝硬化患者的临床治愈率高于对照组(P<0.001)。将接受Peg-IFN-α-2b治疗的患者分为临床治愈组和非临床治愈组进行单因素回归和多因素二元逻辑回归。结果显示,基线qHBsAg[相对比(RR)=0.997,95%CI:[0.995,0.999],P=0.031]和△TBiL(RR=0.698,95%CI:[0.555,0.879],P=0.002)是CHB或代偿期肝硬化患者实现临床治愈的独立影响因素。
较低的基线qHBsAg和治疗24周时TBiL的下降是实现临床治愈的独立影响因素。基线qHBsAg越低,治疗24周后△TBiL水平越高,患者实现临床治愈的概率越高。