The clinical management of hepatic sarcoidosis: A systematic review

IF 1.7 Q3 GASTROENTEROLOGY & HEPATOLOGY JGH Open Pub Date : 2024-06-20 DOI:10.1002/jgh3.13076
Ram Prasad Sinnanaidu, Vikneshwaran Chandra Kumar, Ranita Hisham Shunmugam, Sanjiv Mahadeva
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Abstract

Background

Hepatic sarcoidosis is an uncommon clinical condition in which clear recommendations are lacking in its treatment. We aimed to review systematically the literature on hepatic sarcoidosis treatment to guide clinicians.

Methods

Using MEDLINE, PubMed, CINAHL, Cochrane Library, and Google Scholar databases, we searched original articles on clinical studies reporting the outcome of adult hepatic sarcoidosis patients following treatment with various pharmacological agents. The primary end point was focused on assessing symptomatic relief and biochemical improvement posttreatment.

Results

Out of 614 retrieved references, 34 published studies were eligible, providing data for a total of 268 patients with hepatic sarcoidosis. First-line therapy with corticosteroids alone was reported in 187 patients, whilst ursodeoxycholic acid (UDCA) was used in 40 patients. Symptomatic and biochemical responses were reported among 113(60.4%) and 80(42.8%) cases of corticosteroids respectively, whereas UDCA showed a complete response in 23(57.5%) patients. Second-line therapy was used in steroid-refractory cases, with most cases being reported for azathioprine (n = 32) and methotrexate (n = 28). Notably, 15(46.9%) and 11(39.2%) patients showed both clinical and biochemical responses respectively. Biological therapy including anti-tumor necrosis factor (anti-TNF) was used as third line therapy in twelve cases with a 72.7% symptomatic and biochemical response rate each.

Conclusion

The quality of evidence for the treatment of hepatic sarcoidosis was poor. Nevertheless, it appears that corticosteroid or UDCA may be utilized as first-line therapy. For cases that are refractory to corticosteroids, steroid-sparing immunosuppressive agents and anti-TNF have shown some promising results, but further high-quality studies are required.

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肝肉瘤病的临床治疗:系统综述。
背景:肝肉样瘤病是一种不常见的临床疾病,其治疗缺乏明确的建议。我们旨在系统回顾有关肝肉样瘤病治疗的文献,为临床医生提供指导:我们使用 MEDLINE、PubMed、CINAHL、Cochrane Library 和 Google Scholar 数据库,检索了报告成人肝肉样变性患者接受各种药物治疗后疗效的临床研究原始文章。主要终点集中在评估治疗后症状的缓解和生化指标的改善:在检索到的 614 篇参考文献中,有 34 篇已发表的研究符合条件,共提供了 268 名肝肉样瘤病患者的数据。187名患者接受了单纯皮质类固醇的一线治疗,40名患者接受了熊去氧胆酸(UDCA)治疗。皮质类固醇治疗的 113 例(60.4%)和 80 例(42.8%)患者分别出现了症状反应和生化反应,而 UDCA 治疗的 23 例(57.5%)患者则出现了完全反应。类固醇类药物难治性病例采用二线疗法,大多数病例使用硫唑嘌呤(32 例)和甲氨蝶呤(28 例)。值得注意的是,分别有 15 例(46.9%)和 11 例(39.2%)患者出现了临床和生化反应。包括抗肿瘤坏死因子(anti-TNF)在内的生物疗法作为三线疗法用于12例患者,症状和生化应答率分别为72.7%:结论:治疗肝肉瘤病的证据质量不高。尽管如此,皮质类固醇或 UDCA 似乎仍可作为一线疗法。对于皮质类固醇类药物难治的病例,稀释类固醇的免疫抑制剂和抗肿瘤坏死因子已显示出一些有希望的结果,但还需要进一步的高质量研究。
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来源期刊
JGH Open
JGH Open GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
3.40
自引率
0.00%
发文量
143
审稿时长
7 weeks
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