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培非替尼对两名维持性血液透析类风湿关节炎患者的疗效。

Efficacy of peficitinib in two patients with rheumatoid arthritis on maintenance hemodialysis.

作者信息

Nishimura Akito, Tateiwa Masayuki, Tajima Shuuitirou, Tada Takuya

机构信息

Depratment of Orthopedics, Shimizu Welfare Hospital, 578-1 Ihara-cho, Shimizu-ku, Shizuoka City, Shizuoka 424-0114, Japan.

出版信息

J Rural Med. 2022 Jul;17(3):193-195. doi: 10.2185/jrm.2022-005. Epub 2022 Jul 1.

DOI:10.2185/jrm.2022-005
PMID:35847752
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9263949/
Abstract

Treatment options for patients with rheumatoid arthritis on maintenance hemodialysis with an inadequate response to biologic agents have not been reported. In this report, we describe two patients who achieved remission after treatment with peficitinib. Two 69- and 85-year-old patients with rheumatoid arthritis on maintenance hemodialysis were previously treated with biologics and started on peficitinib 100 mg/day after the secondary failure of biologics. In the two cases presented here, rheumatoid arthritis was almost in remission and there were no adverse events, although the patients were switched to peficitinib after secondary failure of the biologic agents. Among Janus kinase inhibitors, peficitinib has the lowest renal excretion; therefore, its administration in patients on dialysis is not contraindicated according to the package insert in Japan. The use of biologic agents in patients on hemodialysis has been reported to be associated with a high incidence of infections; therefore, care should be taken to avoid infections when administering Janus kinase inhibitors. Janus kinase inhibitors with low renal excretion, such as peficitinib, may be effective in patients with rheumatoid arthritis on maintenance hemodialysis who have an inadequate response to biologic agents.

摘要

对于维持性血液透析且对生物制剂反应不佳的类风湿关节炎患者,尚未有相关治疗方案的报道。在本报告中,我们描述了两名接受培非替尼治疗后病情缓解的患者。两名分别为69岁和85岁的维持性血液透析类风湿关节炎患者,此前接受过生物制剂治疗,在生物制剂二次治疗失败后开始服用培非替尼,剂量为每日100毫克。在本报告的这两个病例中,尽管患者在生物制剂二次治疗失败后改用培非替尼,但类风湿关节炎几乎完全缓解,且未出现不良事件。在Janus激酶抑制剂中,培非替尼的肾脏排泄率最低;因此,根据日本的药品说明书,在透析患者中使用该药并无禁忌。据报道,血液透析患者使用生物制剂会导致感染发生率较高;因此,在使用Janus激酶抑制剂时应注意预防感染。肾脏排泄率较低的Janus激酶抑制剂,如培非替尼,可能对维持性血液透析且对生物制剂反应不佳的类风湿关节炎患者有效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/716f/9263949/ddc73da6b054/jrm-17-193-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/716f/9263949/ac17b77b0b1b/jrm-17-193-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/716f/9263949/ddc73da6b054/jrm-17-193-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/716f/9263949/ac17b77b0b1b/jrm-17-193-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/716f/9263949/ddc73da6b054/jrm-17-193-g002.jpg

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本文引用的文献

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Safety and Effectiveness of Peficitinib (ASP015K) in Patients with Rheumatoid Arthritis: Final Results (32 Months of Mean Peficitinib Treatment) From a Long-Term, Open-Label Extension Study in Japan, Korea, and Taiwan.培非替尼(ASP015K)治疗类风湿性关节炎患者的安全性和有效性:来自日本、韩国及台湾一项长期开放标签扩展研究的最终结果(培非替尼平均治疗32个月)
Rheumatol Ther. 2021 Mar;8(1):425-442. doi: 10.1007/s40744-021-00280-5. Epub 2021 Mar 3.
2
Points to consider for the treatment of immune-mediated inflammatory diseases with Janus kinase inhibitors: a consensus statement.采用 JAK 抑制剂治疗免疫介导的炎症性疾病的相关考量:共识声明。
Ann Rheum Dis. 2021 Jan;80(1):71-87. doi: 10.1136/annrheumdis-2020-218398. Epub 2020 Nov 6.
3
Population pharmacokinetic analysis of peficitinib in patients with rheumatoid arthritis.
类风湿关节炎患者的培非替尼群体药代动力学分析。
Br J Clin Pharmacol. 2021 Apr;87(4):2014-2022. doi: 10.1111/bcp.14605. Epub 2020 Dec 1.
4
Comparative efficacy and safety of tofacitinib, baricitinib, upadacitinib, filgotinib and peficitinib as monotherapy for active rheumatoid arthritis.托法替布、巴瑞替尼、乌帕替尼、费卢替尼和培非替尼单药治疗活动性类风湿关节炎的疗效和安全性比较。
J Clin Pharm Ther. 2020 Aug;45(4):674-681. doi: 10.1111/jcpt.13142. Epub 2020 Jun 3.
5
Pharmacokinetics and Safety of a Single Oral Dose of Peficitinib (ASP015K) in Japanese Subjects with Normal and Impaired Renal Function.在肾功能正常和受损的日本受试者中单次口服培非替尼(ASP015K)的药代动力学和安全性。
Clin Drug Investig. 2020 Feb;40(2):149-159. doi: 10.1007/s40261-019-00873-7.
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