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儿童克罗恩病的抗肿瘤坏死因子治疗:通过优化治疗、更深入了解风险以及因生物类似药的可及性降低成本从而提高疗效

Anti-Tumour Necrosis Factor Therapy for Paediatric Crohn's Disease: Improved Benefits Through Treatment Optimisation, Deeper Understanding of Its Risks, and Reduced Costs due to Biosimilar Availability.

作者信息

Cozijnsen M A, Samsom J N, de Ridder L

机构信息

Department of Paediatric Gastroenterology, Erasmus University Medical Centre-Sophia Children's Hospital, P.O. Box 2060, 3000 CB, Rotterdam, The Netherlands.

Laboratory of Paediatrics, Erasmus University Medical Centre-Sophia Children's Hospital, Rotterdam, The Netherlands.

出版信息

Paediatr Drugs. 2018 Feb;20(1):19-28. doi: 10.1007/s40272-017-0266-9.

DOI:10.1007/s40272-017-0266-9
PMID:29079905
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5775976/
Abstract

Antibodies directed to tumour necrosis factor-α (TNF-α) are very effective in treating paediatric Crohn's disease (CD). Over the last few years, research has provided important new insights into how to optimise this treatment's effectiveness. Research on predictors for anti-TNF treatment responsiveness has revealed potential markers, but data on their accuracy in paediatric CD patients are lagging behind. Also, new evidence has become available on the safety profile of anti-TNF antibodies that suggests the assumed increased malignancy risk seen in patients on anti-TNF and thiopurine combination treatment may be linked more to thiopurine use and not to anti-TNF treatment. In addition, the early results of CT-P13, an infliximab biosimilar, in CD patients confirm the expected similarity with its originator. Thus, the effectiveness of anti-TNF antibody treatment is slowly improving, its malignancy risk is lower than assumed, and its costs are reduced by the introduction of equally effective biosimilars. Together, these trends allow for a more prominent role for anti-TNF antibodies in future treatment of paediatric CD.

摘要

针对肿瘤坏死因子-α(TNF-α)的抗体在治疗儿童克罗恩病(CD)方面非常有效。在过去几年中,研究为如何优化这种治疗的有效性提供了重要的新见解。对抗TNF治疗反应性预测指标的研究已揭示了潜在标志物,但关于其在儿童CD患者中的准确性的数据仍滞后。此外,关于抗TNF抗体安全性的新证据表明,接受抗TNF与硫唑嘌呤联合治疗的患者中假定增加的恶性肿瘤风险可能更多与硫唑嘌呤的使用有关,而非抗TNF治疗。此外,英夫利昔单抗生物类似药CT-P13在CD患者中的早期结果证实了其与原研药预期的相似性。因此,抗TNF抗体治疗的有效性正在缓慢提高,其恶性肿瘤风险低于预期,并且通过引入同样有效的生物类似药降低了成本。总体而言,这些趋势使抗TNF抗体在未来儿童CD治疗中能发挥更突出的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4488/5775976/90b05e15fd65/40272_2017_266_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4488/5775976/5252ec8915ea/40272_2017_266_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4488/5775976/90b05e15fd65/40272_2017_266_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4488/5775976/5252ec8915ea/40272_2017_266_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4488/5775976/90b05e15fd65/40272_2017_266_Fig2_HTML.jpg

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Oncostatin M drives intestinal inflammation and predicts response to tumor necrosis factor-neutralizing therapy in patients with inflammatory bowel disease.制瘤素M可引发肠道炎症,并预测炎症性肠病患者对肿瘤坏死因子中和疗法的反应。
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Prediction of complicated disease course for children newly diagnosed with Crohn's disease: a multicentre inception cohort study.
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Infliximab Is Not Associated With Increased Risk of Malignancy or Hemophagocytic Lymphohistiocytosis in Pediatric Patients With Inflammatory Bowel Disease.英夫利昔单抗治疗儿童炎症性肠病并不增加恶性肿瘤或噬血细胞性淋巴组织细胞增生症的发生风险。
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