Evaluation of the efficacy and safety of conversion from the tacrolimus capsule to tablet in stable liver transplant recipients with maintenance therapy: a 24-week, open-label, single-center, phase IV exploratory clinical study.

IF 16.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Accounts of Chemical Research Pub Date : 2023-10-01 Epub Date: 2023-09-27 DOI:10.4174/astr.2023.105.4.228
Jae-Yoon Kim, Sukyoung Chang, Jiyoung Kim, Hyun Hwa Choi, Jaewon Lee, Su Young Hong, Jeong-Moo Lee, Suk Kyun Hong, YoungRok Choi, Nam-Joon Yi, Kwang-Woong Lee, Kyung-Suk Suh
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Abstract

Purpose: The tablet form of tacrolimus is more convenient for drug ingestion than the capsule form. We examined the efficacy and safety of tacrolimus tablets and a satisfaction survey after formula conversion in liver transplant (LT) recipients.

Methods: This study was an open-label, prospective clinical trial for tacrolimus formula 1:1 conversion from capsule to tablet in 41 adult LT recipients with tacrolimus maintenance therapy of more than 1 month. The primary endpoint was incidence of biopsy-proven acute rejection (BPAR) within 24 weeks. Surveys 1 week before and 4 weeks after formula conversion were conducted for total daily dose of medication, number, scale of discomfort and satisfaction.

Results: The overall incidence of BPAR was 0% and there was no graft loss or patient death. The incidence of adverse effects was 34.1% (n = 14) after formula conversion. The most common severe adverse effect was abnormal liver function test (n = 5): biliary complications (n = 4) and alcoholic recidivism (n = 1). Total daily dose and number of tacrolimus doses were significantly lower after formula conversion (P < 0.05) without changes in trough level. According to survey analysis, there was no significant difference in discomfort and satisfaction scales from capsule to tablet conversion (P < 0.05).

Conclusion: The present study suggests that the new tablet formula can be a useful treatment option to maintain a consistent level of tacrolimus with a lower total daily dose and number in adult LT recipients.

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从他克莫司胶囊转为片剂对稳定肝移植受者进行维持治疗的疗效和安全性评估:一项24周、开放标签、单中心、IV期探索性临床研究。
目的:片剂形式的他克莫司比胶囊形式更便于药物摄入。我们检查了他克莫斯片剂的疗效和安全性,并对肝移植(LT)受者进行了配方转换后的满意度调查。方法:本研究是一项开放性、前瞻性的临床试验,对41名接受他克莫司维持治疗超过1个月的成年LT受试者进行他克莫斯配方从胶囊到片剂的1:1转换。主要终点是24周内活检证实的急性排斥反应(BPAR)的发生率。在配方奶粉转换前1周和转换后4周,对药物的每日总剂量、数量、不适程度和满意度进行了调查。结果:BPAR的总发生率为0%,没有移植物丢失或患者死亡。配方奶粉转换后的不良反应发生率为34.1%(n=14)。最常见的严重不良反应是肝功能异常(n=5):胆道并发症(n=4)和酒精性累犯(n=1)。配方奶粉转换后,他克莫司的日总剂量和剂量数显著降低(P<0.05),谷值没有变化。根据调查分析,从胶囊到片剂的转换,不适和满意度没有显著差异(P<0.05)。
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来源期刊
Accounts of Chemical Research
Accounts of Chemical Research 化学-化学综合
CiteScore
31.40
自引率
1.10%
发文量
312
审稿时长
2 months
期刊介绍: Accounts of Chemical Research presents short, concise and critical articles offering easy-to-read overviews of basic research and applications in all areas of chemistry and biochemistry. These short reviews focus on research from the author’s own laboratory and are designed to teach the reader about a research project. In addition, Accounts of Chemical Research publishes commentaries that give an informed opinion on a current research problem. Special Issues online are devoted to a single topic of unusual activity and significance. Accounts of Chemical Research replaces the traditional article abstract with an article "Conspectus." These entries synopsize the research affording the reader a closer look at the content and significance of an article. Through this provision of a more detailed description of the article contents, the Conspectus enhances the article's discoverability by search engines and the exposure for the research.
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