Chen Zhenlin, Fu Zhiwen, Zhang Nu, Zou Wenbin, Chen Wei
Department of Pharmacy, Fushun People's Hospital, Fushun, China.
Department of Pharmacy, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China.
BMC Pharmacol Toxicol. 2025 Jan 29;26(1):21. doi: 10.1186/s40360-025-00862-x.
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.
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.
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).
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.
细胞周期蛋白依赖性激酶(CDK)-4/6抑制剂显著改善了多种癌症的治疗结果,但也可引发包括肌肉骨骼疾病在内的各种器官系统毒性。本研究旨在基于真实世界数据全面描述与CDK4/6抑制剂相关的肌肉骨骼不良事件(MSAE)。
从FAERS中提取2015年第一季度(Q1)至2023年第四季度与CDK4/6抑制剂相关的MSAE报告。描述性分析评估报告频率随时间的变化以及患者特征。使用报告比值比(ROR)进行不成比例分析,以确定特定肌肉骨骼首选术语(PT)的信号。发病时间分析研究了MSAE的时间模式。
共识别出10,095份与CDK4/6抑制剂相关的MSAE报告,其中大多数涉及哌柏西利(n = 7819)。患者的中位年龄为64岁(四分位间距:55 - 72岁),主要为女性(97.73%)。大多数报告由消费者提交(47.62%),且大多数报告来自美国(71.53%)。不成比例分析揭示了不同的信号,瑞博西尼在骨痛和骨病变方面显示出突出信号,阿贝西利在颌骨坏死和病理性骨折方面显示出突出信号。哌柏西利在所有肌肉骨骼PT方面显示出一致但不太明显的信号。使用非参数Kruskal-Wallis检验,发病时间分析表明,与阿贝西利(32.5天,四分位间距[12 - 119])和瑞博西尼(34天,四分位间距[8 - 177])相比,哌柏西利的MSAE发病时间显著更长(中位82天,四分位间距[14 - 311])(P值 = 3.048e - 11)。
肌肉骨骼毒性是影响药物安全性的重大不良事件。对接受CDK4/6抑制剂治疗的患者而言,早期识别和妥善处理这些事件至关重要。有必要进一步开展研究以阐明潜在机制并改进风险缓解策略。