Musculoskeletal adverse events associated with CDK4/6 inhibitors: a real-world study using FDA Adverse Event Reporting System (FAERS) database.

IF 2.8 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Zhenlin Chen, Zhiwen Fu, Nu Zhang, Wenbin Zou, Wei Chen
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引用次数: 0

Abstract

Objective: Cyclin-dependent kinase (CDK)-4/6 inhibitors have significantly improved outcomes in several cancers but can also induce various organ system toxicities, including musculoskeletal disorders. This study aimed to comprehensively characterize the musculoskeletal adverse events (MSAEs) associated with CDK4/6 inhibitors based on real-world data.

Methods: Reports of MSAEs linked to CDK4/6 inhibitors from the first quarter (Q1) of 2015 and 2023 Q4 were extracted from the FAERS. Descriptive analyses evaluated report frequencies over time and patient characteristics. Disproportionality analyses using reporting odds ratios (RORs) identified signals for specific musculoskeletal preferred terms (PTs). Time-to-onset analyses examined the temporal patterns of MSAEs.

Results: A total of 10,095 MSAE reports associated with CDK4/6 inhibitors were identified, most involving Palbociclib (n = 7819). The median age of patients was 64 years (IQR: 55-72), predominantly female (97.73%). Most reports were submitted by consumers (47.62%) and the majority of reports were from the United States (71.53%). Disproportionality analyses revealed distinct signals, with Ribociclib showing prominent signals for bone pain and bone lesions, and Abemaciclib for osteonecrosis of the jaw and pathological fractures. Palbociclib demonstrated a consistent but less pronounced signal across musculoskeletal PTs. Time-to-onset analyses demonstrated a significantly longer onset of MSAEs for Palbociclib (median 82 days, IQR[14-311]) compared to Abemaciclib (32.5 days, IQR[12-119]) and Ribociclib (34 days, IQR[8-177]) using the nonparametric Kruskal-Wallis test (P-value = 3.048e-11).

Conclusion: Musculoskeletal toxicities is a significant adverse event that affects drug safety. Early identification and proper management of these events are crucial for patients receiving CDK4/6 inhibitors. Further research is warranted to elucidate the underlying mechanisms and improve risk mitigation strategies.

与CDK4/6抑制剂相关的肌肉骨骼不良事件:一项使用FDA不良事件报告系统(FAERS)数据库的真实世界研究
目的:细胞周期蛋白依赖性激酶(CDK)-4/6抑制剂可显著改善几种癌症的预后,但也可诱导各种器官系统毒性,包括肌肉骨骼疾病。本研究旨在基于真实数据全面表征与CDK4/6抑制剂相关的肌肉骨骼不良事件(MSAEs)。方法:从FAERS中提取2015年第一季度(Q1)和2023年第四季度与CDK4/6抑制剂相关的msae报告。描述性分析评估了随时间变化的报告频率和患者特征。歧化分析使用报告优势比(RORs)识别特定肌肉骨骼首选术语(PTs)的信号。发病时间分析检查了MSAEs的时间模式。结果:共鉴定出10095例与CDK4/6抑制剂相关的MSAE报告,其中大多数涉及帕博西尼(n = 7819)。患者年龄中位数为64岁(IQR: 55-72),以女性为主(97.73%)。大多数报告由消费者提交(47.62%),大多数报告来自美国(71.53%)。歧化分析显示了不同的信号,Ribociclib显示了骨痛和骨病变的显著信号,而Abemaciclib显示了颌骨骨坏死和病理性骨折的显著信号。帕博西尼在肌肉骨骼PTs中表现出一致但不太明显的信号。使用非参数Kruskal-Wallis检验(p值= 3.048e-11),发病时间分析显示Palbociclib的msae发病时间(中位82天,IQR[14-311])明显高于Abemaciclib(32.5天,IQR[12-119])和Ribociclib(34天,IQR[8-177])。结论:肌肉骨骼毒性是影响药物安全性的重大不良事件。对于接受CDK4/6抑制剂治疗的患者来说,这些事件的早期识别和适当管理至关重要。有必要进行进一步的研究,以阐明潜在的机制和改进风险缓解战略。
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
BMC Pharmacology & Toxicology
BMC Pharmacology & Toxicology PHARMACOLOGY & PHARMACYTOXICOLOGY&nb-TOXICOLOGY
CiteScore
4.80
自引率
0.00%
发文量
87
审稿时长
12 weeks
期刊介绍: BMC Pharmacology and Toxicology is an open access, peer-reviewed journal that considers articles on all aspects of chemically defined therapeutic and toxic agents. The journal welcomes submissions from all fields of experimental and clinical pharmacology including clinical trials and toxicology.
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