Efficacy of rituximab-containing regimens used as first-line and rescue therapy for giant cell hepatitis with autoimmune hemolytic anemia a retrospective study

IF 2.6 4区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY Clinics and research in hepatology and gastroenterology Pub Date : 2024-06-17 DOI:10.1016/j.clinre.2024.102392
Xue-Yuan Zhang , Jing-Yu Gong , Jian-She Wang , Jia-Yan Feng , Lian Chen , Xin-Bao Xie , Yi Lu
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Abstract

Objective

To evaluate the efficacy of rituximab (RTX)-containing therapy as first-line as well as rescue treatment for giant cell hepatitis with autoimmune hemolytic anemia (GCH-AHA).

Methods

This retrospective study recruited patients diagnosed with GCH-AHA and treated with conventional immunosuppressor regimens consisting of prednisone or RTX-containing regimes consisting of RTX and prednisone, with or without another immunosuppressor. The primary outcomes were the complete remission (CR) rate and time-period required for CR. The secondary outcomes included relapses and adverse events.

Results

Twenty patients (8 females and 12 males; age range 1–26 months), 15 receiving conventional regimens and 5 receiving RTX-containing regimens, were included. The CR rates were 73.3 % (11/15) and 100 % (5/5) in the conventional and RTX-containing groups, respectively. The time-period required for CR was significantly shorter in the RTX-containing group than in the conventional group (6 (3–8) versus 14 (5–25) months, P = 0.015). Relapses occurred in 30.8 % (4/13) of patients in the conventional group; all achieved CR after adding RTX. Relapses occurred in 40.0 % (2/5) of patients in the RTX-containing group; both achieved CR after adding intravenous immune globulins or tacrolimus. Transient low immunoglobulin and infections were recorded in both groups. Treatment withdrawal was achieved in 73.3 % (11/15) and 60.0 % (3/5) of patients receiving conventional and RTX-containing regimens after 36 (2–101) and 22 (4–41) months, respectively. Two patients in conventional group died of disease progression and infection.

Conclusions

RTX-containing first-line therapy achieves CR of GCH-AHA more quickly than the conventional therapy. RTX is efficacious when added to rescue therapy.

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含利妥昔单抗方案作为巨细胞性肝炎合并自身免疫性溶血性贫血的一线治疗和抢救治疗的疗效回顾性研究。
目的评估含利妥昔单抗(RTX)疗法作为巨细胞性肝炎伴自身免疫性溶血性贫血(GCH-AHA)一线治疗和抢救治疗的疗效:这项回顾性研究招募了被诊断为GCH-AHA的患者,他们接受了由泼尼松组成的传统免疫抑制剂治疗方案,或由RTX和泼尼松组成的含RTX治疗方案,同时使用或不使用另一种免疫抑制剂。主要结果是完全缓解率和完全缓解所需时间。次要结果包括复发和不良反应:共纳入20名患者(8名女性和12名男性;年龄范围为1-26个月),其中15名接受常规方案治疗,5名接受含RTX方案治疗。常规组和含RTX组的CR率分别为73.3%(11/15)和100%(5/5)。含RTX组获得CR所需的时间明显短于常规组(6(3-8)个月对14(5-25)个月,P=0.015)。常规治疗组中有 30.8%(4/13)的患者复发;在添加 RTX 后,所有患者都达到了 CR。含 RTX 组有 40.0%(2/5)的患者复发;在加入静脉注射免疫球蛋白或他克莫司后,两组患者均获得了 CR。两组患者均出现了短暂的免疫球蛋白低下和感染。接受常规和含 RTX 方案治疗的患者中,分别有 73.3%(11/15)和 60.0%(3/5)的患者在 36 个月(2-101)和 22 个月(4-41)后停药。常规组有两名患者死于疾病进展和感染:结论:与传统疗法相比,含RTX的一线疗法能更快达到GCH-AHA的CR。结论:与传统疗法相比,含RTX的一线疗法能更快地达到GCH-AHA的CR。
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来源期刊
CiteScore
4.30
自引率
3.70%
发文量
198
审稿时长
42 days
期刊介绍: Clinics and Research in Hepatology and Gastroenterology publishes high-quality original research papers in the field of hepatology and gastroenterology. The editors put the accent on rapid communication of new research and clinical developments and so called "hot topic" issues. Following a clear Editorial line, besides original articles and case reports, each issue features editorials, commentaries and reviews. The journal encourages research and discussion between all those involved in the specialty on an international level. All articles are peer reviewed by international experts, the articles in press are online and indexed in the international databases (Current Contents, Pubmed, Scopus, Science Direct). Clinics and Research in Hepatology and Gastroenterology is a subscription journal (with optional open access), which allows you to publish your research without any cost to you (unless you proactively chose the open access option). Your article will be available to all researchers around the globe whose institution has a subscription to the journal.
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