Anamorelin and Conduction Defects: A Literature Review and Analysis of the Japanese Pharmacovigilance Database.

IF 1.8 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
In vivo Pub Date : 2025-01-01 DOI:10.21873/invivo.13842
Naohiro Yabuki, Ken-Ichi Sako, Tomoji Maeda, Naohito Ide
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引用次数: 0

Abstract

Background/aim: Cancer cachexia is characterized by weight loss with a specific decrease in skeletal muscle and adipose tissue. In Japan, anamorelin, which has a novel mechanism of action, was approved in 2021 for the treatment of cancer cachexia. However, little information is available on its safety in routine clinical care, in particular the occurrence of conduction defects as adverse reactions. Therefore, this study evaluated the risk and time to onset of anamorelin-related conduction defects by performing a literature review and evaluating the Japanese pharmacovigilance database.

Patients and methods: We reviewed the literature from April 2000 to June 2024 to identify reports of anamorelin-related conduction defects and analyzed data from April 2004 to December 2023 in the Japanese Adverse Drug Event Report (JADER) database. Using the database, we calculated reporting odds ratios (RORs) with 95% confidence intervals (CIs) and adjusted RORs (95%CIs) by considering whether patients were taking concomitant medications that can cause QT prolongation. In addition, we investigated outcomes and time to onset.

Results: The literature review identified seven cases of conduction defects. All cases occurred within approximately three weeks after starting treatment, and all patients recovered. The JADER database contained 537 cases of adverse reactions to anamorelin. The adjusted ROR (95%CI) of conduction defects was 20.00 (14.86-26.91), and the median time to onset was 13 days. Poor clinical outcomes occurred in only a few cases.

Conclusion: Performing frequent cardiac electrograms for two to three weeks after starting anamorelin may help to quickly identify anamorelin-related conduction defects.

Anamorelin与传导缺陷:日本药物警戒数据库的文献回顾与分析。
背景/目的:癌症恶病质的特征是体重减轻,骨骼肌和脂肪组织特异性减少。在日本,anamorelin具有一种新的作用机制,于2021年被批准用于治疗癌症恶病质。然而,关于其在常规临床护理中的安全性,特别是传导缺陷作为不良反应的发生率的信息很少。因此,本研究通过文献回顾和评估日本药物警戒数据库来评估anamorelin相关传导缺陷的风险和发病时间。患者和方法:我们回顾了2000年4月至2024年6月的文献,以确定与anamorelin相关的传导缺陷的报告,并分析了2004年4月至2023年12月日本不良药物事件报告(JADER)数据库中的数据。使用该数据库,我们以95%置信区间(ci)计算报告优势比(RORs),并通过考虑患者是否同时服用可导致QT间期延长的药物来调整RORs (95% ci)。此外,我们调查了结果和发病时间。结果:通过文献复习,发现7例传导缺损。所有病例均发生在开始治疗后约三周内,所有患者均康复。JADER数据库包含537例anamorelin不良反应。传导缺损的校正ROR (95%CI)为20.00(14.86 ~ 26.91),中位发病时间为13天。仅有少数病例出现不良临床结果。结论:在开始使用阿纳莫瑞林后2 - 3周频繁进行心脏心电图检查有助于快速识别阿纳莫瑞林相关的传导缺陷。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
In vivo
In vivo 医学-医学:研究与实验
CiteScore
4.20
自引率
4.30%
发文量
330
审稿时长
3-8 weeks
期刊介绍: IN VIVO is an international peer-reviewed journal designed to bring together original high quality works and reviews on experimental and clinical biomedical research within the frames of physiology, pathology and disease management. The topics of IN VIVO include: 1. Experimental development and application of new diagnostic and therapeutic procedures; 2. Pharmacological and toxicological evaluation of new drugs, drug combinations and drug delivery systems; 3. Clinical trials; 4. Development and characterization of models of biomedical research; 5. Cancer diagnosis and treatment; 6. Immunotherapy and vaccines; 7. Radiotherapy, Imaging; 8. Tissue engineering, Regenerative medicine; 9. Carcinogenesis.
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